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2/4 Trigeminal Neuralgia , TN, aka tic douloreaux,

Click Slide Show Draft for New TN Patients.  Bookmark this page now!
 

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Welcome,

Trigeminal Neuralgia , TN, tic douloreaux, is the trigeminal nerve producing  false signals from the brain sending excruciating lightening strikes of facial pain to one side of the face.  Treatment is by medication, radiosurgery, craniofacial surgery or neurosurgery  or Microvascular Decompression  (MVD) for nerve pain relief. Trigeminal Neuralgia typically is near the nose lips, eyes, or ears.

This  compendium is also "Brian's Pain Journal". Let me hear about your face pain. I can publish on the web  anything you have to say about  trigeminal neuralgia. It will help other with face pain.  We can become "Pain Pals". The cause and permanent cure for
tic douloreaux (TN) are still unknown.  If your group would like a speaker about TN  call me. 

This letter is for the record and to keep a PAIN JOURNAL of where the above stated title problem stands. 

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Page 5 of 7 Tim Guith Sections 101 to 125 Opiods

http://www.BrianNelsonConsulting.com/trigeminal-neuralgia-tn/tim-guith.html  UD 09/06/2006 12:11:19 PM -0500

 Page 6 of 7 Bilateral Facial Pain and Bitter Taste in the Mouth. http://www.briannelsonconsulting.com/trigeminal-neuralgia-tn/bilateral-facial-pain.html 

Page 7 of 7 Patient Painful Stories  You are at: http://www.BrianNelsonConsulting.com/trigeminal-neuralgia-tn/patient-painful-stories.html

You can find this site again  by typing  the word "neuralgia1" backwards, ie.  OR "1aiglaruen"in Google. Brian "

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If after you scan to the bottom of this  website and still can't find the information you are looking for try another Google search here.
Contact information for this Website:
 
Brian Nelson, Webpage Marketing Consultant 

 31 Gessner Rd. Houston, TX  09/06/2006 12:11 PM -0500
713-467-3025  Fax 713-467-3192  
Click: E-mail me
Trigeminal Neuralgia, aka Tic douloreaux  or  TN
&
Temporomandibular  Joint aka TMJ  Eventually Cancer.This website is about Brian Nelson's fight with a parotid (salivary) gland tumor. It started out with the symptoms of  Trigeminal Neuralgia, aka Tic douloreaux  or  TN & Temporomadibular Joint aka TMJ Click Here to see my other record file at IAmFightingCancer.com  Bookmark this page now!  
 
Scan down to read my very lengthy and detailed web journal. Call me if I can help you. 713-467-3025 Brian
Signature Card For:                 Brian Nelson    31 Gessner Rd. , Houston, TX  77024
Tel. 713-467-3025 (Refers to my cell)      Fax 713-467-3192        
Click here to e-mail me.

www.NelsonIdeas.com
       Make a difference in the world!  "Idea Possibility Consulting"
www.BrianNelsonConsulting.com    There are so many new ways to make more profit. 
www.PartyTentCity.com 
                                The best modular party tent you can buy!
www.IamFightingCancer.com   Brian's story on Cancer and TN.  Post your Cancer story!

Bookmark this page now!

Misspelled Words on this pagetrigemnal, trigeminal, trigemial, trigeminl, tigeminal, trgeminal, trieminal, trigminal, trigeinal, trigeminar, tligeminal, tligeminar, tr1gen1ma1, tr1gen1mal, trigenimal, trigemimal, trigeminla, trigemianl, trigemnial, trigeimnal, trigmeinal, triegminal, trgieminal, tirgeminal, rtigeminal, trigemina, rigeminal, neuralgia, nuralgia, neralgia, neualgia, neurlgia, neuragia, neuralia, neuralga, neurargia, neurargai, neulalgia, neulalgai, neulargia, neulargai, neuralgai, neura1g1a, neuralg1a, meuralgia, neuraliga, neuraglia, neurlagia, neuarlgia, nerualgia, nueralgia, enuralgia, neuralgi, euralgia, tic, tik, tick, t1c, tci, itc,dou1oreaux, douloreaxu, douloreuax, douloraeux, douloeraux, doulroeaux, douolreaux, doluoreaux, duoloreaux, oduloreaux, douloreau, douloreax, douloreux, douloraux, douloeaux, doulreaux, douoreaux, doloreaux, duloreaux, ouloreaux, douloreaux,tenporomad1bu1ar, tenporomad1bular, tenporomadibular, temporomadibulra, temporomadibualr, temporomadibluar, temporomadiublar, temporomadbiular, temporomaidbular, temporomdaibular, temporoamdibular, tempormoadibular, tempoormadibular, temproomadibular, temopromadibular, tepmoromadibular, tmeporomadibular, etmporomadibular, temporomadibula, temporomadibulr, temporomadibuar, temporomadiblar, temporomadiular, temporomadbular, temporomaibular, temporomdibular, temporoadibular, tempormadibular, tempoomadibular, tempromadibular, temoromadibular, teporomadibular, tmporomadibular, emporomadibular, temporomadibular

Trigeminal Neuralgia, aka Tic douloreaux  or  TN
& Temporomadibular Joint
aka
TMJ  Eventually Cancer.

Trigeminal Neuralgia , TN, tic douloreaux, is the trigeminal nerve producing  false signals from the brain sending excruciating lightening strikes of facial pain to one side of the face. Compendium

Trigeminal Neuralgia , TN, tic douloreaux, is the trigeminal nerve producing  false signals from the brain sending excruciating lightening strikes of facial pain to one side of the face.  Treatment is by medication, radiosurgery, craniofacial surgery or neurosurgery  or Microvascular Decompression  (MVD) for nerve pain relief. Trigeminal Neuralgia typically is near the nose lips, eyes, or ears.

This  compendium is also "Brian's Pain Journal". Let me hear about your face pain. I can publish on the web  anything you have to say about  trigeminal neuralgia. It will help other with face pain.  We can become "Pain Pals". The cause and permanent cure for
tic douloreaux (TN) are still unknown.  If your group would like a speaker about TN  call me. 

Page 4 of 6.

 
by  Brian Nelson
bnelson@PartyTentCity.com

713-467-3025 Houston,  TX 

  Hi Aiglaruen

1 Brian Nelson
www.BrianNelsonConsulting.com
http://www.Internet-Marketing-Sales-Strategies.com
www.PartyTentCity.com
31 Gessner Rd.
Houston,  TX  77024
713-467-3025,  Fax  713-467-3192
 bnelson@PartyTentCity.com

Research on Brian's Pain Management.

What Is Trigeminal Neuralgia?

Brian Nelson’s Report Pain on Left side of Head.
Document Initiated on 8-22-04  Last update 8-30-04 620am ..

Brian Nelson, 31 Gessner Rd. , Houston, TX  77024
bnelson@PartyTentCity.com  , 713-467-3025 .

This letter is for the record and to keep a PAIN JOURNAL of where the above stated title problem stands. 

 Page 1 of 4 Section 1-25
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You  are at Page 4 of 4 Section 76-100
http://www.BrianNelsonConsulting.com/trigeminal-neuralgia-tn/faq-info4.html   ud 09/06/2006 12:11 PM -0500

Here is an interesting MVD website about surgery successes. I am surprised it was on the net.   http://www.hfs-assn.org/surgery.htm 

 MTNSB   Include page Pending Paste.


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76 From: http://facial-neuralgia.org/conditions/tn-gn.html

GLOSSOPHARYNGEAL NEURALGIA
Conditions: Other Cranial Disorders

Disclaimer.

Glossopharyngeal Neuralgia is described as a deep stabbing pain in one side of the throat. The pain is near the tonsil area and can extend into the ear. Thomas J. Lovely, M.D. , Peter J. Jannetta, M.D. of the University of Pittsburgh have a brief discussion on their experiences treating this condition at: Glossopharyngeal Neuralgia.

Links:

Glossopharyngeal Neuralgia - Singapore Journal 1999

Medline on Glossopharyngeal Neuralgia

Merk Manual-- glossopharyngeal neuralgia

Glossopharyngeal neuralgia, CCND Winnipeg

Glossopharyngeal neuralgia University of Pittsburgh

Glossopharyngeal Neuralgia , B.Todd Troost

The following article goes into greater detail although it does not discuss microvascular decompression surgery as a possible treatment..

The following article is excerpted from:
 
THE MANAGEMENT OF PAIN,
VOL 1, Second Edition, 1990, Lea & Febiger, Philadelphia]
CRANIAL NEURALGIAS
John D. Loeser

This article is posted here in compliance with the FAIR USE DOCTRINE and is for educational purposes only, not for commercial use.

"Glossopharyngeal neuralgia is characterized by shock like pains in the territory of the glossopharyngeal nerve. It is in every way similar to tic douloureux except for the distribution of the pain and the customary site of the triggering stimulus.

Etiology

"The vast majority of patients with glossopharyngeal neuralgia are thought to have an artery compressing the nerve as it exits from the medulla and travels through the subarachnoid space to the jugular foramen. This syndrome can be seen in patients with multiple sclerosis, but it is rare.

Symptoms and Signs

"Glossopharyngeal neuralgia is characterized by excruciating shock-like-pain in the region of the tonsilar fossa, pharynx, or base of the tongue. It can radiate to the ear or the angle of the jaw or into the upper lateral neck. The trigger zone is often in the same area, and patients frequently report that swallowing, yawning, clearing the throat, or talking is the precipitating stimulus. The pain often appears to be spontaneous. Chewing or touching the face does not precipitate an attack. Glossopharyngeal neuralgia is much less common than tic douloureux---the incidence ratio is about 1:100.

Diagnosis

"The nature of the pain, its description by the patient, and the chronology of the attacks are identical to those of tic douloureux of the trigeminal nerve. Indeed, glossopharyngeal tic is sometimes mistaken for mandibular division trigeminal tic douloureux. Involvement of the glossopharyngeal nerve can be demonstrated by localizing the triggering stimulus to the pharyngeal structures that it innervates. Blocking the trigger area with local anesthetic can confirm the site of the trigger and nerve involvement. This is unsuccessful in some patients because the vagus nerve can contain the involved sensory fibers. The role of the glossopharyngeal nerve in the regulation of heart rate and blood pressure is thought to be why some patients with glossopharyngeal neuralgia have profound cardiac arrhythmia's and even asystole with the attack of pain. The presence of such phenomena guarantees that the pain syndrome involves this nerve. The diagnosis can be confirmed by the cessation of pain when this nerve is blocked at the jugular foramen or when topical anesthesia of the pharynx stops the pain.

Treatment

"The pharmacologic management is the same as that for tic douloureux of the trigeminal nerve. When medical management fails, suboccipital craniectomy with exploration of the glossopharyngeal nerve is indicated. If a compressing blood vessel is found it can be mobilized, and the pain usually stops without any loss of nerve function. When no structural pathology can be identified, the glossopharyngeal nerve should be Sectioned. In such a case it is wise to Section the upper fibers of the vagus nerve as well, because they can also be involved in the pain syndrome. When rhizotomy is unsuccessful, which happens rarely, the medial aspect of the descending tract of the trigeminal nerve can be Sectioned to produce loss of pain and temperature sensation in the pharynx.

"A percutaneous technique of glossopharyngeal neurolysis has been described, but it has not been widely used because of cardiovascular and laryngeal complications. "

 

Trigeminal Neuralgia, aka Tic douloreaux  or  TN
&
Temporomandibular  Joint aka TMJ  Eventually Cancer.This website is about Brian Nelson's fight with a parotid (salivary) gland tumor. It started out with the symptoms of  Trigeminal Neuralgia, aka Tic douloreaux  or  TN & Temporomadibular Joint aka TMJ Click Here to see my other record file at IAmFightingCancer.com  Bookmark this page now!  
 
Scan down to read my very lengthy and detailed web journal. Call me if I can help you. 713-467-3025 Brian
Hi,
1. CLICK for the very low priced Web Hosting service I use. Click Here for Prices or
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Brian
Signature Card For:                 Brian Nelson    31 Gessner Rd. , Houston, TX  77024
Tel. 713-467-3025 (Refers to my cell)      Fax 713-467-3192        
Click here to e-mail me.

www.NelsonIdeas.com
       Make a difference in the world!  "Idea Possibility Consulting"
www.BrianNelsonConsulting.com    There are so many new ways to make more profit. 
www.PartyTentCity.com 
                                The best modular party tent you can buy!
www.IamFightingCancer.com   Brian's story on Cancer and TN.  Post your Cancer story!
77 From: http://www.gwc.maricopa.edu/class/bio201/cn/cranial.htm Go to this site to click on 12 cranial nerves which light up when you put your cursor over it.

Cranial Nerves:
Review Info
 
 
 
 

  There are 12 pairs of cranial nerves.
  Olfactory I
  Optic II
  Oculomotor III
  Trochlear IV
  Trigeminal V
  Abducens VI
  Facial VII
  Auditory (vestibulocochlear) VIII
  Glossopharyngeal IX
  Vagus X
  Spinal Accessory XI
  Hypoglossal XII
 

To help memorize each, a mnemonic is often used by students such as . . .
"On Old Olympic Towering Tops A Finn And German Viewed Some Hops"
Cranial Nerve:        Major Functions:
I Olfactory        smell
II Optic        vision
III Oculomotor        eyelid and eyeball movement
IV Trochlear        innervates superior oblique
turns eye downward and laterally
V Trigeminal        chewing
face & mouth touch & pain
VI Abducens        turns eye laterally
VII Facial        controls most facial expressions
secretion of tears & saliva
taste
VII Vestibulocochlear
(auditory)
       hearing
equillibrium sensation
IX Glossopharyngeal        taste
senses carotid blood pressure
X Vagus        senses aortic blood pressure
slows heart rate
stimulates digestive organs
taste
XI Spinal Accessory        controls trapezius & sternocleidomastoid
controls swallowing movements
XII Hypoglossal        controls tongue movements

 

78
Trigeminal neuralgia  From http://www.healthatoz.com/healthatoz/Atoz/ency/trigeminal_neuralgia.jsp
 

 

Definition

Trigeminal neuralgia is a disorder of the trigeminal nerve (the fifth cranial nerve) that causes episodes of sharp, stabbing pain in the cheek, lips, gums, or chin on one side of the face.

Description

The trigeminal nerve, which is divided into three branches, is responsible for chewing, for producing saliva and tears, and for sending facial sensations to the brain. When this nerve breaks down for some reason, it can trigger brief but agonizing sizzles of pain on one side of the face.

This condition is unusual in those under age 50 and more often occurs after 70. Women are three times more likely to have the condition than are men. When trigeminal neuralgia does occur in younger people, it is often associated with multiple sclerosis.

The pain, while brief, is so severe that the sufferer often can't do anything else while the attack lasts. People with this pain often wince or twitch, which is where trigeminal neuralgia gets its French nickname tic douloureux, meaning "painful twitch."

Causes and symptoms

The origin of trigeminal neuralgia is not certain, but scientists believe it may be caused by degeneration, pressure, or irritation of the trigeminal nerve. Some doctors believe the pain may be triggered by pressure from a nearby abnormally-formed artery lying too close to the nerve.

Any part of the three branches of the trigeminal nerve may be affected. Neuralgia of the first branch leads to pain around the eyes and over the forehead; the second branch causes pain in the upper lip, nose and cheek; the third branch causes pain on the side of the tongue and lower lip.

The first episodes are usually fairly mild and brief, and it may be minutes, hours, or weeks before the next attack. However, attacks tend to occur in clumps that may last for weeks at a time. As the sufferer ages, the episodes become more frequent and painful, until the person begins to live in constant fear of the next one.

The momentary bursts of pain usually begin from the same spot on the face each time. The pain can be triggered by touching the area, washing, shaving, eating, drinking, or even talking. Even a cool breeze across the face can set off an attack. Pain is more severe at the ends of the affected nerve, especially over the lip, chin, nostrils, or teeth.

Diagnosis
Diagnosis is usually made by eliminating other problems that could cause similar pain in teeth, jaw, head, or sinuses. Because patients with the condition tend to avoid trigger points, avoiding chewing, shaving, touching or washing their faces can be a clue to diagnosis of trigeminal neuralgia.

Treatment

It is not easy to treat trigeminal neuralgia. Pain can be suppressed by a range of medicines, including the anti-epilepsy medicines carbamazepine (Tegretol) or phenytoin (Dilantin). These drugs slow down the nerve signals at certain nerve terminals, which eases the pain. However, these drugs cause a wide range of side effects, including nausea, dizziness, drowsiness, liver problems, and skin allergies. Some people develop resistance to the drugs or they can't tolerate the high dosage needed to control the discomfort. If the medicines are stopped, the pain usually returns.

If drug treatment fails, surgical treatment to block pain signals from the nerve may be effective. Radio-frequency waves, gamma rays, or glycerol injections can deaden the nerve (and hence the pain). An operation that frees the nerve from whatever is compressing it (blood vessel or tumor) can permanently relieve pain, but this major neurosurgical procedure carries its own risks and complications. Alternatively, a new procedure seeks to place a cushioning sponge between the nerve and a pulsating artery wrapping around it to soothe the irritated nerve.

Prognosis

Although the pain is momentarily incapacitating, it's not life-threatening. As the person ages, the attacks can be expected to occur more and more frequently.

Prevention

While the condition itself can't be prevented, there are a number of things patients can do to avoid triggering attacks:

 

  • wash with cotton pads and warm water over the face

     

     

  • rinse the mouth with water after eating, if toothbrushing triggers pain

     

     

  • eat and drink food and beverages at room temperature

     

     

  • chew on the unaffected side

     

     

  • eat soft foods, if eating is becoming a problem

 

79  From http://swnt240.swmed.edu/swneurosurg/tn.htm

Trigeminal Neuralgia and
Vascular Compression Syndromes

 

Trigeminal neuralgia is a face pain syndrome characterized by electric like shock pain that is generally on one side of the face, comes in waves and is often triggered by light touch, brushing of teeth, eating or even talking. It is often misdiagnosed as dental pain or jaw pain and can even be dismissed as "nothing" by inexperienced physicians.

Trigeminal neuralgia is thought to be caused by compression of the nerve that supplies sensation to the face by an aberrant loop in a normal brain blood vessel. Treatment options include observation, medication and various types of surgical procedures to alleviate the pain. No one treatment is right for everyone so we feel it is best to be treated in an environment where multiple treatment modalities are available. Results of the surgical treatment of trigeminal neuralgia are linked to the experience of the surgeon. We believe it is important to only undergo treatment by a neurosurgeon who has familiarity with the disease.

Other vascular compression syndromes exist.  Trigeminal neuralgia is compression of the fifth cranial nerve and results in pain. Compression of the seventh cranial nerve causes hemifacial spasm, a twitching of one side of the face that flares and remits during the course of a day.  Glossopharyngeal neuralgia is compression on the ninth nerve and causes a pain similar to trigeminal neuralgia but in the back of the throat rather then on the face. These other compression syndromes also respond to therapy.

Face pain can be caused by things other then trigeminal neuralgia. Traumatic nerve injury, dental pain, jaw pain and stroke can all cause various types of atypical face pain. The treatment of these types of face pain depends on making the proper diagnosis and customizing therapy. Treatment also needs to be directed to the secondary effects of chronic pain.

80  Osteonecrosis of the Jaw  From http://www.diagnose-me.com/cond/C547513.html
   
     
   

Neuralgia-inducing Cavitational Osteonecrosis (NICO) has been described in medical literature since 1976 and is known under a number of names including: Ratner bone cavities, alveolar cavitational osteopathosis, Robert's bone cavity, trigger point bone cavity, interference field and, most commonly, NICO. In cases of NICO it is claimed that small areas of bone in the upper or lower jaw become infected or inflamed and die, producing neuralgia-like pain. Most often, no sign of inflammation appears on X-ray. NICO is said to appear after tooth extraction, jaw surgery, endodontic therapy or crown preparation and is speculated to be the result of a long-standing low-grade infection.

The pain felt is constant and is often burning and cramping, much like atypical facial pain symptoms. Usually there are trigger points immediately over the areas of infected jawbone that will produce pain when pressed. NICO can cause "referred pain" in that the neuralgia-like symptoms are "referred" to other parts of the face, intraoral cavity and head.

Some cases of NICO appear to be caused or aggravated by infection. Others speculate that minor trauma from extractions, root canal and other dental procedures are common initiators of NICO but believe this only happens in people already susceptible because of a pre-existing blood clotting disorder. Some believe that NICO can develop when blood vessels are injured in the area, resulting in poor circulation which in turn can lead to bone death.

It is difficult to diagnose this problem as the pain symptoms often are similar to other conditions such as Myofascial Pain Disorder (MPD), Temporal Mandibular Joint (TMJ) problems, atypical facial pain, trigeminal neuralgia, phantom toothache, or headache. X-rays of the jawbone most often appear normal. However, a bone biopsy of the affected area can show positive signs of jawbone inflammation.

Discussion
NICO is not generally accepted as a cause of Trigeminal Neuralgia by most medical and dental professionals. It is possible that NICO is involved in some cases of facial neuralgia, especially atypical facial pain. One long-term study has reported considerably or totally reduced pain in 74% of facial neuralgia patients who had jawbone curettage. However, the pain returned for about 30% of these patients, of whom most had been diagnosed with either TN or atypical facial pain.

In dental circles there appears to be two distinct schools of thought on NICO. Some medical and dental professionals consider NICO a controversial diagnosis. Not only do they not consider it a possible cause of trigeminal neuralgia or other facial neuralgias, they also doubt the condition exists as a disorder. They point to data suggesting bone cavitations are found routinely in cadaver jawbones, casting doubt on the theory that bone cavities cause facial neuralgias.

Other dentists believe NICO is the culprit in many facial pain syndromes and that these painful conditions can be cured by jawbone curettage (scraping and removing infected tissue). They point to studies that show a high success rate for jawbone curettage. Some of these dentists believe that root canals and mercury fillings are partly responsible for NICO.

Signs, symptoms & indicators of Osteonecrosis of the Jaw:

Symptoms - Nervous   Shooting/having constant facial pain

Risk factors for Osteonecrosis of the Jaw:

Circulation   Hypercoagulation (Thickened Blood)

Osteonecrosis of the Jaw can lead to:

Nervous System   Trigeminal Neuralgia / Facial Pain

Recommendations and treatments for Osteonecrosis of the Jaw:

Surgery/Invasive   Surgery
  The only known treatment for NICO is jawbone curettage, in which the jawbone is opened, the infected area drilled out, and the bone biopsied to confirm the presence of inflammation or infection. Often the bone cavity is packed with antibiotics such as teramyacin. A course of antibiotic treatment may be prescribed. Jawbone curettage is not currently done routinely, and it is too early to say whether or not it will ever become generally accepted.
Trigeminal Neuralgia, aka Tic douloreaux  or  TN
&
Temporomandibular  Joint aka TMJ  Eventually Cancer.This website is about Brian Nelson's fight with a parotid (salivary) gland tumor. It started out with the symptoms of  Trigeminal Neuralgia, aka Tic douloreaux  or  TN & Temporomadibular Joint aka TMJ Click Here to see my other record file at IAmFightingCancer.com  Bookmark this page now!  
 
Scan down to read my very lengthy and detailed web journal. Call me if I can help you. 713-467-3025 Brian
Signature Card For:                 Brian Nelson    31 Gessner Rd. , Houston, TX  77024
Tel. 713-467-3025 (Refers to my cell)      Fax 713-467-3192        
Click here to e-mail me.

www.NelsonIdeas.com
       Make a difference in the world!  "Idea Possibility Consulting"
www.BrianNelsonConsulting.com    There are so many new ways to make more profit. 
www.PartyTentCity.com 
                                The best modular party tent you can buy!
www.IamFightingCancer.com   Brian's story on Cancer and TN.  Post your Cancer story!
81 From http://www.ninds.nih.gov/health_and_medical/disorders/trigemin_doc.htm
NINDS Trigeminal Neuralgia Information Page
Synonym(s):  Tic Douloureux
Reviewed  05-29-2001   Get Web page suited for printing
Email this to a friend or colleague
Table of Contents (click to jump to sections)

What is Trigeminal Neuralgia?
Is there any treatment?
What is the prognosis?
What research is being done?

Organizations
Related NINDS Publications and Information

What is Trigeminal Neuralgia?
Trigeminal neuralgia, also called tic douloureux, is a condition that affects the trigeminal nerve (the 5th cranial nerve), one of the largest nerves in the head. The trigeminal nerve is responsible for sending impulses of touch, pain, pressure, and temperature to the brain from the face, jaw, gums, forehead, and around the eyes. Trigeminal neuralgia is characterized by a sudden, severe, electric shock-like or stabbing pain typically felt on one side of the jaw or cheek. The disorder is more common in women than in men and rarely affects anyone younger than 50. The attacks of pain, which generally last several seconds and may be repeated one after the other, may be triggered by talking, brushing teeth, touching the face, chewing, or swallowing. The attacks may come and go throughout the day and last for days, weeks, or months at a time, and then disappear for months or years.

Is there any treatment?
Treatment for trigeminal neuralgia typically includes anticonvulsant medications such as carbamazepine or phenytoin. Baclofen, clonazepam, gabapentin, and valproic acid may also be effective and may be used in combination to achieve pain relief. If medication fails to relieve pain, surgical treatment may be recommended.

What is the prognosis?
The disorder is characterized by recurrences and remissions, and successive recurrences may incapacitate the patient. Due to the intensity of the pain, even the fear of an impending attack may prevent activity. Trigeminal neuralgia is not fatal.

What research is being done?
Within the NINDS research programs, trigeminal neuralgia is addressed primarily through studies associated with pain research. NINDS vigorously pursues a research program seeking new treatments for pain and nerve damage with the ultimate goal of reversing debilitating conditions such as trigeminal neuralgia. NINDS has notified research investigators that it is seeking grant applications both in basic and clinical pain research.

82  From: http://www.tna-support.org/newlook/conference_files/2nd%20Natl%20Conf/Dental.htm

Report of the Trigeminal Neuralgia Association
Second National Conference,

November 11-15, 1998
Orlando FL

TN and Dental Problems

Dental problems loom large for anyone with TN because the trigeminal nerve goes to both face and teeth. Some people are initially misdiagnosed by a dentist and have unnecessary root canals and/or extractions. Later on, major dental work can make the pain of TN worse or it can end a remission.

Dentist Brian D. Fuselier: It's true that TN is often diagnosed only after the patient has had a number of unnecessary dental procedures. My colleagues and I are trying to educate dentists to consider TN when they're diagnosing facial pain.

Dentists assume that when prodding a tooth produces severe pain, it is usually caused by pulpitis (inflammation of the pulp or nerve of the tooth) and the appropriate treatment is a root canal. If that doesn't help, the dentist may do a second root canal on another tooth.  Eventually, the patient may have one or more teeth extracted. All this dental treatment may be unnecessary.

The first thing a dentist should do in diagnosing pain is to make sure the patient has a true dental problem. If the pain is not dental, it could be caused by a number of different conditions, including TN. To make a diagnosis, the dentist should ask questions about the quality of the pain - is it throbbing, stabbing, electrical, continuous, etc. - and about its intensity, duration and frequency, as well as its location.

Dentist Parker E. Mahan: Dentists differentiate between types of pain by taking an extensive medical history and examining the teeth, jaw muscles, salivary glands, blood vessels, mucus membranes, and temporomandibular joints. There are several facial pain syndromes that are sometimes confused with TN. They include:

Atypical odontalgia, or atypical toothache: It's atypical because X-rays show nothing wrong with the tooth but it hurts. This often occurs in 30- to 50-year-old women who are depressed. However, the pain is real.

There are a number of theories about the cause of it. Some suggest that the disorder originates in the blood vessels or the sympathetic nervous system. When patients take a tricyclic antidepressant like imipramine (Tofranil) for three-toeight weeks, half find that the pain goes away.

Myofascial pain dysfunction (MPD):  People who clench their teeth repeatedly while they sleep (a problem called bruxism) can develop pain in the muscles on the sides of the face. Hard knots appear within the muscles; squeezing a knot produces shooting pain. If a dentist injects a local anesthetic into these knots, they become soft. The injection disrupts the muscle, but it heals in three weeks. To prevent the pain from returning after that, it's necessary to prevent bruxism, perhaps with a bite splint worn at night.
 
 
Before doing a root canal, should a dentist use Tegretol to make sure the patient doesn't have TN? (If facial pain is relieved by Tegretol, that strongly suggests that it may be caused by TN.)

Dr. Fuselier: If a dentist is uncertain about whether the pain truly is a dental problem, it would be appropriate to refer the patient to a pain-management specialist, such as a neurologist, who has been trained in the use of Tegretol.

Neurosurgeon John M. Tew Jr: Sometimes patients demand that one or more teeth be extracted. If the dentist refuses them, they go looking for someone else who will agree to pull the teeth.

What is being done to educate dentists about TN?

Dr. Gremillion: At dental conferences there are presentations about facial pain, including TN, and dental schools have a growing interest in teaching their students about it. Currently there is strong pressure on the American Association of Dental Schools to make training in facial pain a mandatory part of a dentist's education.
 

 

"A family practitioner may see two cases of trigeminal neuralgia in a lifetime. A dentist may go ten years without seeing a true case of TN." - Dr. Albert Rhoton.

A Precursor to TN
Dr. Gremillion:
Dentists sometimes see a pain problem that appears to be a precursor to trigeminal neuralgia. It can occur months or even decades before full-blown TN, and the procedure used to diagnose the  problem often produces a respite.

In this condition, the pain is sometimes sporadic, sharp, and stabbing, like classic TN, but more typically it's a dull ache or it can feel like sinus pain or a toothache. It may be constant or may come and go, lasting minutes or hours each time. There is no specific trigger zone on the face but chewing, drinking hot or cold liquids, yawning, talking, or brushing teeth can brin on the pain. It is often localized at first. Over time it may spread to involve a larger area or move to another site. To make a diagnosis, the dentist numbs the area with a long-acting local anesthetic. If the pain came from a tooth, it will soon return. If it was produced by TN, relief may continue after the anesthetic wears off. In some cases, a series of injections of local anesthetic can relieve pain for months or even years.

How to Prevent TN Flare-ups after Dental Work
Why does dental work often trigger a new attack of TN for someone who is in remission?  Why does it tend to make the problem worse for those who have their pain under control with medications? Is there any way to prevent these things from happening?

Dentist Parker E. Mahan: After all of the surgical procedures used to treat TN, some patients experience a breakthrough of pain. It probably doesn't take much stimulation to trigger that breakthrough.

TN presents a paradox. On one hand, it's of the utmost importance to maintain good dental health in order to avoid problems that might precipitate, an upsurge of pain. On the other hand, because major dental work can aggravate the Trigeminal nerve, you should have only procedures that are truly necessary - for instance, don't agree to let your dentist replace a very large filling with a crown if the filling is still serviceable.

If you must have major work done, I recommend pre-emptive anesthesia to prevent the pain of the dental procedure from "jazzing up" the transmission of pain signals from the trigeminal nerve to the brain.  

  • For a day or so before and after the procedure, increase the dose of any TN medications you're taking.
  • Ask your dentist to use Marcaine without epinephrine for the local anesthetic. You may need to ask in advance because the average dentist doesn't keep this particular drug in stock. Marcaine is long-acting, so you're less likely to need multiple injections - each one producing pain signals. Epinephrine is a vasoconstrictor; added to a local anesthetic, it prevents blood flow from carrying away the anesthetic and thus prolongs its numbing effect. However, epinephrine can trigger nerve pain, so you're better off without it.
     
  • Ask the dentist to inject the local anesthetic at a site as far as possible from the trigger point for the TN pain.
     
  • Several hours before the procedure, take a pain-killing medication. Opioids such as codeine are good at preempting pain. After the procedure, take the painkiller again.  The goal is to have at least five hours afterwards during which you're free of pain.
     
  • If dental procedures make you very nervous, consider foregoing local anesthesia. You can have laughing gas or IV anesthesia instead to reduce emotional trauma.

If you have TN, is it better to have a root canal or to have a problem tooth pulled? Dr. Langan: Provided an extraction isn't contraindicated for some reason, I believe it is often a better solution than a root canal because the trauma is short-lived, minimizing painful stimulation of the central nervous system.

What can you do to maintain good dental hygiene when it hurts too much to brush your teeth? Dr. Langan: Ask your dentist to prescribe a topical anesthetic called viscous lidocaine and use it to numb your mouth. If that doesn't help, try a prescription mouth rinse called Peridex, an oral antibiotic. It can sometimes stain the teeth, so wipe off your teeth as best you can. Drink only lukewarm fluids to keep from stimulating the nerves in your mouth. When the pain flare-up is over, remember that if you have TN, good dental hygiene means having your teeth cleaned by your dentist at least twice a year.

 

83 The term bruxism is defined as;
                                   “to grind the teeth, a clenching of the teeth, associated with forceful jaw movements,
                                     resulting in rubbing, gritting, or grinding together of the teeth, usually during sleep.”

What causes bruxing to occur?
This is a very difficult question to answer. Some researchers say that if the occlusion (bite) of someone is not correct they will brux. Others say that it is a central nervous system disorder. Others say it is a multifaceted problem.

For all practical purposes……EVERYONE  bruxes. Therefore, the question is NOT whether a person does in fact brux. Rather, the better question is to what degree do they brux. There is not a scale of bruxing that exists, but, we could imagine that there is such a scale. This scale could run from a 1 indicating a very very slight habit to a 10+ which would indicate a severe bruxer. A person at level 1 would not show any signs of bruxing at all. On the other hand the  people in the higher end on the scale would show one or several signs. The pressure that can be generated across the teeth can range from 100 to 600psi (pounds per square inch) this is an incredible amount of force. The problems outlined below occur as a result of these forces being applied over many years -  slowly - and it can be difficult to recognize the cause/effect sequence.

Possible signs, complications or damage that may occur are:

  1. Wearing of teeth.
    Wear occurs from the movement of the teeth harshly against one another. Although all teeth may show this type wear, it is especially noticeable when a person has front teeth that appear having the same length - as if they were filed down.
  2. Breaking of teeth.
    As teeth wear, the edges of front teeth and the cusps or corners of back teeth will begin to show microfractures or cracks. These cracks can not be seen on x-rays. It takes magnified vision and/or an intraoral magnified image to diagnose them. Where this becomes especially important, is that teeth with these type of fractures will either eventually chip, break a corner, or yet require root canal therapy. The reason for root canal therapy is that the fracture begins on the surface of the tooth and eventually deepens until the crack enters the area of the nerve.
  3. Sensitive teeth.
    Usually a generalized soreness and/or a cold sensitivity..
  4. Receeding gums and/or teeth with gum line “notches”.
    Most people have been told or assume that receeding gums occur because of age, using a hard bristle brush or the occurence of gum (periodontal) disease. In fact none of these reasons are correct in a majority of the cases. These are  referred to as abrasion areas. When teeth grind hard against each other year after year, they flex at the gum line and the enamel (which ends thinly at the gum line) microfractures away. The end result is an area at the gum line that you can catch your fingernail in and may get extremely sensitive to touch and/or cold.

     
    brux.jpg (11239 bytes) In this picture, there is exposed root surface 
    and advanced abrasion areas.
  5. Loose teeth
    Teeth loosen because of the "rocking" back forth that occurs. The best analogy is the example of getting a fence post out of the ground by rocking it back and forth.
  6. Periodontal pockets (loss of supporting bone around the teeth).
    Sometimes instead of the tooth getting loose, there may be a generalized horizontal loss of supporting bone and/or localized areas of bone loss.
  7. Bony ridges (tori)
    Instead of losing bone support - some people actually form "extra" bone to support the teeth (this appears as bony ridges that can be seen and felt on the jaw bones as a smooth raised area about at the level of the roots.
    brux1.jpg (11419 bytes) brux2.jpg (6742 bytes)
    This image is of the lower jaw showing
    extra bone in the "floor" of  the mouth
    by the tongue.
    This picture shows the cheeks
    pulled back and the ridge along
      and above the upper back teeth.
  8. Cheek irritation - A ridge or line of fibrosed (toughened) tissue on the inside of the cheek that corresponds to where the teeth come together. Sometimes a person will actually bite themselves along this line (especially in the most posterior molar area).
  9. Sore muscles (especially in the cheek and temple area) When these two muscles are overused. They may get sore - just like when you over exercise, your other muscles get sore.

                                
    10. Headaches (especially upon waking in the same muscle areas mentioned above).
          Instead of soreness, the muscle aches will appear as a headache.
   11. TMJ problems (jaw joint pain / soreness / etc)
         The jaw joint may be over loaded and resulting problems occur.

       These signs take time (usually decades of years) to show themselves.

Does everyone show every problem? No they don't, we are all very different. Some of us will exhibit none of these problems (thank your genetic code for that), some of us will exhibit severe problems (curse your genetic code for that).  So any combination, or NO problems may exist for any one person.

So, what should anyone do about bruxism? Is there a cure?

This is a very difficult thing to answer. For a large number of people, the problem is that their bite is off - this triggers through a series of physiological signals, a dramatic increase in the amount of bruxing.

STRESS is a huge factor when it comes to bruxing. In fact the mouth can show stress before any other area of the body. The more stress, the more bruxing and the harder the bruxing.

NIGHTGUARD
It would be logical to think that an acrylic nightguard is simply a piece of plastic used to cover and prevent the teeth from coming together while sleeping at  night. This is true - BUT - most importantly, when in place it provides a correct bite so that muscles will relax and problems in a persons bite will not trigger the bruxing action.. The aspect of making and delivering a nightguard CORRECTLY is difficult to explain but you may see this process by clicking here. A point needs to be made that tooth wear still slowly occurs when using a nightguard. The reason for this is that a person (especially severe bruxers) will clench and very slightly grind during the day time when their guard is not being worn. 

A nightguard is NOT a solution, rather a method of greatly decreasing  the damage caused by bruxing. It is possible to alter a bite so that a guard may not be needed - the method varies from case to case.

84
bruxismbruxism



Do you suffer from painful jaws or experience headaches in the morning ? Does your spouse complain that you keep him or her up all night ? Have your teeth become more sensitive to cold , touch, or other stimuli ? If so you may be one of the millions of people who unknowingly suffers from bruxism (tooth grinding).
What is Bruxism ?
 

Bruxism, commonly known as tooth grinding, is the the clenching together of the bottom and upper jaw accompanied by the grinding of the lower set of teeth with the upper set. Bruxism affects between 10-50% of the population depending on the particular study sited. Bruxism is a subconscious behavior so many people do not realize that they are doing it ! Often it is the partner who tells them about the nighttime sounds that their bruxism produces.

Although it can occur during the waking hours, bruxism most frequently occurs while we sleep. During sleep, the biting force (the force at which the jaws clench together) can be up to six times greater than the pressure during waking hours. Consequently, significant damage is much more likely to occur with this nighttime bruxism.
The Results of Bruxism

Bruxism can lead to pain and cause damage to gums and other oral structures. This includes:

    Sore Facial Muscles, Headaches, and Ear-Aches
    The muscles used to chew food are the same ones responsible for bruxism. Consequently, these muscles often feel sore or tender in the morning. This may make the jaw feel tight or may cause pain when the sides of the mouth are touched. Often this muscle pain is referred meaning that it manifests itself as a headache, ear-ache, or neck pain.

    Cosmetic Damage
    Bruxism can cause the teeth to be ground down becoming significantly shortened and creating cosmetic damage.

    Sensitive Teeth
    As the enamel of the tooth is worn away by bruxism the underlying dentin layer of the tooth is exposed. This causes the tooth to become sensitive to cold, pressure, and other stimuli.

    Fractured Teeth and Fillings
    The high pressure created from bruxism can fracture teeth and crack fillings.

    Temporomandibular Joint Damage
    Bruxism can cause damage to the temperomandibular joint. This is the "hinge" which connects the lower jaw to the upper jaw allowing use to chew and talk.

How to Treat Bruxism

If you suspect that you suffer from bruxism see your dentist. They can tell you if your symptoms are in fact due to bruxism. In most cases, they can create a custom mouth guard for you to wear while you sleep. The mouth guard takes the punishment that your teeth would normally endure during your bruxism. This will minimize the damage associated with bruxism.

Additionally, your dentist may help you properly position your teeth and tongue so as to reduce your bruxism. Reducing alcohol intake is also advisable since alcohol has been shown to worsen bruxism.

It is now well known that stress and anxiety play the major role in causing bruxism. If you suffer from bruxism try to more effectively manage the stress in your life. By carefully monitoring and controlling the stress you can often dramatically reduce bruxism

85 SLEEP BRUXISM (TOOTH-GRINDING OR TEETH-CLENCHING) INFORMATION  Updated November 30, 1998

What is Sleep Bruxism?

Sleep Bruxism is a sterotyped movement disorder characterized by grinding or clenching of the teeth during sleep.  The disorder has also been identified as nocturnal bruxism, nocturnal tooth-grinding and nocturnal tooth-clenching.

What are the Symptoms?

The symptoms of Sleep Bruxism are tooth-grinding or tooth-clenching during sleep that may cause:

  • abnormal wear of the teeth
  • sounds associated with bruxism (It's about as pleasant as fingernails on a chalkboard!)
  • jaw muscle discomfort

How serious is the disorder?

Some people have episodes that occur less than nightly with no evidence of dental injury or impairment of psychosocial functioning. And others experience nightly episodes with evidence of mild impairment of psychosocial functioning. Yet others have nightly episodes with evidence of dental injury, tempomandibular (jaw) disorders, other physical injury or moderate or severe impairment of psychosocial functioning.

When someone with suspected sleep bruxism has a polysomnographic test there is evidence of jaw muscle activity during the sleep period and the absence of abnormal movement during sleep.  Other sleep disorders may be present at the same time, e.g., obstructive sleep apnea, restless legs syndrome.

Damage to the teeth needs to be stopped. Pain and injury to the jaw may require surgery.

How is it treated?

If the damage is not advanced, your dentist can make you a mouthguard that fits over your lower set of teeth and prevents the two sets of teeth from grinding against each other. See below for treatments using neurofeedback to reduce stress, etc

Trigeminal Neuralgia, aka Tic douloreaux  or  TN
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86     From: http://facial-neuralgia.org/conditions/atfp.html

ATYPICAL FACIAL PAIN
Conditions:  Facial Neuralgias

DISCLAIMER.

| DESCRIPTION | POSSIBLE CAUSES | SYMPTOMS | DIAGNOSIS 
| TREATMENTS | ONLINE RESOURCES |

DESCRIPTION
Atypical Facial Pain (ATFP) is a syndrome encompassing a wide group of facial pain problems. ATFP can have many different causes but the symptoms are all similar. Facial pain, often described as burning, aching or cramping, occurs on one side of the face, often in the region of the trigeminal nerve and can extend into the upper neck or back of the scalp. Although rarely as severe as trigeminal neuralgia, facial pain is continuous for ATFP patients, with few, if any periods of remission. Recent studies propose that ATFP is an early form of trigeminal neuralgia. Indeed, some patients have components of both ATFP and TN symptoms.  Earlier literature has linked ATFP to "psychological pathology." Recent studies, however have shown no such link exists.

POSSIBLE CAUSES
ATFP has many possible causes. In some cases, infections of the sinuses or teeth appear to be involved. Some studies postulate a   low-grade infectious and inflammatory process occurring over a long period can result in nerve damage and be the triggering factor for ATFP pain. Some believe that vascular compression of the trigeminal nerve in the same area that is postulated to lead to trigeminal neuralgia is a cause of ATFP although studies have shown that microvascular decompression rarely leads to pain relief in ATFP patients. Dental or some sort of physical trauma is also linked to ATFP. Several somewhat controversial studies postulate that a condition known as NICO - Neuralgia Inducing Cavitational Osteonecrosis is the cause of the neuralgia-like symptoms of atypical facial pain.

SYMPTOMS
Facial pain, often described as burning, aching or cramping, pinching, pulling, occurs on one side of the face, often in the region of the trigeminal nerve and can extend into the upper neck or back of the scalp. Although rarely as severe as trigeminal neuralgia, facial pain is continuous for ATFP patients, with few, if any periods of remission.

DIAGNOSIS
Diagnosing atypical facial pain is not an easy task. It's not unusual for ATFP patients to have undergone numerous dental procedures, seen multiple doctors and undergone many medical tests before being successfully diagnosed and treated. A diagnosis of ATFP is usually a process of elimination. When a patient complains of constant facial pain restricted to one side of the face, the physician must first rule out any other conditions. Tests include roentgenograms of the skull, MRI and/ or CT scan with particular attention to the skull base, careful dental and otolaryngolgic evaluation, and thorough neurological examination. Only after tests rule out other factors can a diagnosis of ATFP be made.

TREATMENTS
Treatment of ATFP can be difficult and perplexing for both doctor and patient. Medication is usually the first course of treatment. Surgical procedures such as microvascular decompression generally are not successful with ATFP patients.

The following drugs are used to treat atypical facial pain:

bullet5.gif (101 bytes) Amitriptyline. (Triptyl, Elavil)
bullet5.gif (101 bytes)  Gabapentin. (Neurontin).
bullet5.gif (101 bytes)  Pamelor
bullet5.gif (101 bytes)  Capsaicin

Other pain relief strategies include:

bullet5.gif (101 bytes) Hot and cold compresses|
bullet5.gif (101 bytes) Acupuncture
bullet5.gif (101 bytes)  Biofeedback
Dental Splint

ONLINE RESOURCES
Professional Websites

Atypical Facial Pain
Excellent discussion of Atypical Facial Pain from emedicine.com

87 From: http://www.emedicine.com/neuro/topic25.htm
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Atypical Facial Pain

Last Updated: February 9, 2001

 
 
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Author: James H Halsey, MD, Professor, Department of Neurology, University of Alabama Medical Center
James H Halsey, MD, is a member of the following medical societies: American Academy of Neurology, American Heart Association, American Medical Association, American Neurological Association, American Society of Neuroimaging Society, Medical Association of the State of Alabama, New York Academy of Sciences, Pan American Medical Association, Sigma Xi, Society for Neuroscience, and Southern Medical Association
Editor(s): Joseph R Carcione, Jr, DO, MBA, Consultant in Neurology and Medical Acupuncture, Medical Management and Organizational Consulting, Central Westchester Neuromuscular Care, PC; Medical Director, Oxford Health Plans; Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, Pharmacy, eMedicine; Robert Egan, MD, Assistant Professor, Departments of Ophthalmology and Neurology, Portland VAMC, Casey Eye Institute, Oregon Health Sciences University; Selim R Benbadis, MD, Director of Comprehensive Epilepsy Program, Associate Professor, Departments of Neurology and Neurosurgery, University of South Florida, Tampa General Hospital; and Helmi L Lutsep, MD, Associate Director, Oregon Stroke Center, Associate Professor, Department of Neurology, Oregon Health Sciences University
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Background: Atypical facial pain occurs in the territory of the trigeminal nerve, but the discomfort is not typical of trigeminal neuralgia. It may be as severe as trigeminal neuralgia, but its pattern and quality are different. Whereas trigeminal neuralgia is characterized by quick episodes of jabbing or lancinating pain, atypical facial pain is usually burning, aching, dull, or crushing. Moreover, an individual atypical facial pain attack always lasts longer than a few seconds and usually lasts minutes or hours (if not continuous). The distinction is important for making treatment decisions, because surgery, usually rhizotomy or vascular decompression, is highly effective for trigeminal neuralgia, whereas surgery is not appropriate for atypical facial pain.

A variation of atypical facial pain is discomfort similar to that of trigeminal neuralgia (eg, lancinating) but atypical in location (eg, far lateral on the face or in the occipital area). Some writers classify these as neuralgias of other nerves (in these examples, superficial temporal or occipital).

Frequency:
 

  • In the US: Although accurate figures are not possible because of the lack of agreement on criteria for classification, atypical facial pain is approximately one fifth as frequent as trigeminal neuralgia. The incidence of trigeminal neuralgia is 4-5 per 100,000 per year.

Race: No racial predilection is known.

Sex: Atypical facial pain affects both sexes with approximately equal frequency.

Age: The disorder mainly affects adults and is rare in the young.

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History: Atypical facial pain must be distinguished from trigeminal neuralgia. It also must be distinguished from temporomandibular joint (TMJ) syndrome, migraine, and cluster headache.

  • Trigeminal neuralgia is characterized by severe bursts of pain in one or more branches of the trigeminal nerve.
    • The bursts are quick, repetitive jabs of pain (lancinations). Each pain episode is only an instant in duration; the episodes recur irregularly many times a minute.
    • Trigeminal neuralgia episodes are not in synchrony with the heartbeat or pulse (usually slower).
    • The patient may wince, twitch, or cry out when a series of pain jabs occurs.
    • The pain is excruciating.
  • Atypical facial pain may be as severe as trigeminal neuralgia, but its pattern and quality are different.
    • Pain episodes are always longer than a few seconds, lasting minutes to hours, and are sometimes continuous. The duration of the individual episode helps to make the distinction.
    • The pain is dull, aching, crushing, or burning.
    • Occasionally, patients use terms such as "sharp" or "knifelike" to describe the pain.
  • TMJ syndrome is recognized by the following:
    • The location and quality of pain may be similar to those of atypical facial pain.
    • TMJ syndrome is characterized by focal tenderness of one or both TMJs and aggravation of pain by chewing, talking, and lateral jaw movement.
    • Pharmacologic treatment is usually unsuccessful.
    • Treatment of TMJ syndrome (by an oral surgeon) often is directed at either the arthropathy of the joint itself or at fatigue and spasm of the pterygoid and temporalis muscles.
  • Migraine is recognized by the following signs and symptoms. Diagnosis of migraine may be acceptable if some of these features are absent, but generally at least 3 should be present. The essential feature is recurrent, severe headache with normal neurologic examination and blood pressure.
    • Female-to-male ratio is 3:1.
    • Pain is throbbing and synchronous with the heartbeat or pulse, usually on only one side of the head. Headache may be accompanied by scalp tenderness.
    • Photophobia and sonophobia are common associated symptoms.  
    • Nausea often accompanies migraine.  
    • Patients often describe an aura at the onset.  
    • Sleep (if it can be achieved) can abort a migraine. 
    • Pharmacologic therapy, typically with ergotamine, isometheptene, or serotonin receptor agonists of the triptan family, is highly effective for migraine, almost to the point of diagnostic specificity. These agents are ineffective in atypical facial pain.
  • Cluster headache, in terms of effective pharmacologic therapy, is closely related to migraine. Pain location and quality sometimes may be confused with atypical facial pain. Characteristics of cluster headaches include the following: 
    • Male-to-female ratio is 6:1.
    • Pain awakens patient from sleep 
    • Onset of pain is sudden.  
    • Episodes typically last minutes (but can last hours).  
    • Pain is intense, crushing, or burning. 
    • Pain recurs frequently up to several times a day in clusters of several days to weeks.  
    • Strictly unilateral, the pain often is associated with ipsilateral conjunctival injection and nasal congestion.  
    • Unlike migraine, cluster headache is very responsive to inhaled oxygen (ie, abortive) therapy.

Physical:

  • Neurologic and physical examinations are usually normal. Trigger points, where pain is evoked by stimulation, are rare.
  • The supraorbital or infraorbital foramen may be locally tender. Significant tenderness at one or both TMJs would favor the diagnosis of TMJ syndrome.

Causes:

  • Atypical facial pain is usually without a specific cause. However, injury of any peripheral or proximal branch of the trigeminal nerve due to facial trauma or basal skull fracture can produce the disorder.
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Brainstem Gliomas
Chronic Paroxysmal Hemicrania
Cluster Headache
Headache: Pediatric Perspective
Migraine Headache
Migraine Headache: Neuro-Ophthalmic Perspective
Migraine Headache: Pediatric Perspective
Migraine Variants
Temporomandibular Joint Syndrome
Trigeminal Neuralgia

Other Problems to be Considered:

Brainstem syndromes
Chronic pain programs
Malignant and nonmalignant pain syndromes

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Brainstem Gliomas

Chronic Paroxysmal Hemicrania

Cluster Headache

Headache: Pediatric Perspective

Migraine Headache

Migraine Headache: Neuro-Ophthalmic Perspective

Migraine Headache: Pediatric Perspective

Migraine Variants

Temporomandibular Joint Syndrome

Trigeminal Neuralgia

 

 


 

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Imaging Studies:

  • A brain MRI scan with gadolinium is the imaging modality of choice, although most studies will be normal. Examples of possible lesions include neuromas or cysts involving the trigeminal root or its distal branches outside the brain and malignancies of the skull base compressing or invading a branch of the nerve.
  • CT scan of the head with contrast has a lower yield than MRI because of its poorer resolution of the brain stem and cranial nerves.
  TREATMENT Section 6 of 9   Click here to go to the previous section in this topic Click here to go to the top of this page Click here to go to the next section in this topic
Author Information Introduction Clinical Differentials Workup Treatment Medication Miscellaneous Bibliography
 

Medical Care:

  • Medical treatment of atypical facial pain is less satisfactory than that of trigeminal neuralgia, reflecting the etiologic, symptomatic, and nosologic heterogeneity of the two conditions. Of the nonnarcotic drugs, tricyclic antidepressants give best results; phenytoin is of intermediate effectiveness, and carbamazepine is least effective. Any of these may be best in a particular patient.
  • Of the new anticonvulsants, gabapentin and lamotrigine show promise, but their efficacy relative to the older drugs has not been established.
  • In patients whose pain is typical of trigeminal neuralgia (eg, lancinating) but atypical in location, carbamazepine is usually most effective, phenytoin of intermediate effectiveness, and tricyclics the least effective; gabapentin and lamotrigine retain their broad-spectrum positions.
  • For neuropathic pain in any location, the same principle applies. For lancinating pain, the usual order of effectiveness is carbamazepine first, phenytoin intermediate, and tricyclics last. The reverse order is true for burning and other pain types.
  • Aching joint pain and abdominal cramps are least likely to respond to these drugs. In all situations, the quality of pain is more important than its location.
  • Narcotic treatment is sometimes appropriate as an adjunct but requires careful supervision, usually in collaboration with the patient's pharmacist. The most effective program is to provide a monthly ration of narcotic that is strictly enforced and documented. Older patients fare better with narcotics since the risk of addiction is low in patients older than 70 years.

Surgical Care:
Surgical treatment, by section of the infraorbital nerve, maxillary nerve, or sphenopalatine ganglion, is sometimes effective.
 

    • Because of the risk of anesthesia dolorosa, surgery should be reserved for cases of medical intractability with repeated demonstration of pain interruption by nerve block.
    • A new procedure appropriate in carefully selected cases is stereotactic trigeminal root entry zone nucleotomy.

Consultations:

  • All treatments should be provided in cooperation with the patient's primary care physician.


  MEDICATION Section 7 of 9   Click here to go to the previous section in this topic Click here to go to the top of this page Click here to go to the next section in this topic
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The goal of therapy is to manage the pain with anticonvulsants and antidepressants. Narcotics may be appropriate if administered under careful supervision.
 

Drug Category: Tricyclic antidepressants -- A complex group of drugs that have central and peripheral anticholinergic effects and sedative effects. They block the active reuptake of norepinephrine and serotonin.

Drug Name
 
Amitriptyline (Elavil) -- Increases synaptic concentration of serotonin and/or norepinephrine in CNS by inhibiting reuptake by presynaptic neuronal membrane. Useful as analgesic for certain types of chronic and neuropathic pain.
Adult Dose 30-100 mg/d PO hs
Pediatric Dose Children: 0.1 mg/kg PO hs; increase, as tolerated, over 2-3 wk to 0.5-2 mg/d hs
Adolescents: 25-50 mg/d PO hs; increase gradually to 100 mg/d in divided doses
Contraindications Documented hypersensitivity, patients who have taken MAOIs in past 14 d
Interactions Because metabolized by P 450 2D6 system, other drugs that inhibit this enzyme system (eg, cimetidine, quinidine) may increase tricyclic levels; phenobarbital may increase metabolism, decreasing effects; blocks uptake of guanethidine and prevents its hypotensive effects; may interact with thyroid medications, alcohol, CNS depressants, barbiturates, and disulfiram
Pregnancy D - Unsafe in pregnancy
Precautions May have pronouced effects in cardiovascular system; use cautiously in elderly patients or those with cardiac conduction disturbances or history of hyperthyroidism or renal or hepatic impairment
Drug Name
 
Nortriptyline (Aventyl hydrochloride, Pamelor) -- Has demonstrated effectiveness in treatment of chronic pain. Increases synaptic concentration of serotonin and/or norepinephrine in CNS by inhibiting their reuptake by presynaptic neuronal membrane. Additional pharmacodynamic effects, such as desensitization of adenyl cyclase and downregulation of beta-adrenergic receptors and serotonin receptors, appear to play roles.
Adult Dose 25 mg PO tid/qid; not to exceed 150 mg/d
Pediatric Dose <25 kg: Not recommended
25-35 kg: 10-20 mg/d PO
35-54 kg: 25-35 mg/d PO
Contraindications Documented hypersensitivity, narrow-angle glaucoma, patients who have taken MAOIs in past 14 d
Interactions Cimetidine may increase levels; may increase PT in patients stabilized on warfarin
Pregnancy D - Unsafe in pregnancy
Precautions Use cautiously in patients with renal or hepatic impairment, cardiac conduction disturbances, or history of hyperthyroidism

Drug Category: Anticonvulsants -- Although useful, their mechanism of action in neuropathic pain is unknown.

Drug Name
 
Carbamazepine (Tegretol, Carbatrol, Epitol) -- Has antineuralgic effects; may depress activity of nucleus ventralis of thalamus or decrease synaptic transmission or summation of temporal stimulation, leading to neural discharge by limiting influx of sodium ions across cell membrane or other unknown mechanisms. Target blood serum concentrations 4-12 mg/L.
Adult Dose 200 mg PO bid initial dose; increase gradually prn over 2 wk to 200 mg tid; sustained-release form: therapeutic dose bid
Pediatric Dose <6 years: 10-20 mg/kg/d PO initial dose; titrate dose prn 6-12 years: 100 mg PO bid initial dose; titrate dose prn >12 years: 200 mg PO bid initial dose; titrate dose prn
Contraindications Documented hypersensitivity, bone marrow suppression, MAOIs
Interactions Cyclosporine, oral contraceptives, tricyclic antidepressants, warfarin, phenytoin, doxycycline, neuroleptics, fentanyl, calcium channel blockers, macrolide antibiotics, isoniazid, cimetidine, lamotrigine, propoxyphene
Pregnancy C - Safety for use during pregnancy has not been established.
Precautions MAOIs should be discontinued for minimum of 14 d before starting carbamazepine; use cautiously in patients with history of cardiac damage or hepatic disease; blood cell abnormalities have been reported following this medication; may worsen primary generalized epilepsy or atypical absence seizures; 0.5-1% risk of spina bifida in children born to mothers who take carbamazepine during pregnancy
Drug Name
 
Gabapentin (Neurontin) -- Has properties common to other anticonvulsants and antineuralgic effects. Exact mechanism of action not known. Structurally related to GABA but does not interact with GABA receptors.
Adult Dose 300 mg PO hs on day 1; increase to 400 mg PO tid over 3-d interval and titrate dose prn; not to exceed 1200 mg qid
Pediatric Dose <12 years: Not established >12 years: Administer as in adults
Contraindications Documented hypersensitivity
Interactions Antacids can reduce bioavailability by 20%; cimetidine may decrease clearance; may increase levels of norethindrone
Pregnancy C - Safety for use during pregnancy has not been established.
Precautions Abrupt withdrawal may precipitate seizures; use caution when treating patients with renal impairment
Drug Name
 
Phenytoin (Dilantin) -- May stabilize neuronal membranes and treat neuralgia by increasing efflux or decreasing influx of sodium ions across cell membranes in motor cortex during generation of nerve impulses. When serum level in or near therapeutic range, adjust dose in 30- to 50-mg increments. Small-dose increments may cause greater than expected increases in serum concentration (ie, Michaelis-Menten drug kinetics). Steady-state serum levels may take up to 3 wk to occur, because half-life is concentration dependent.
Adult Dose 300 mg/d PO initial dose; adjust to maintain serum levels of 10-20 mg/L
Pediatric Dose 5 mg/kg/d PO bid
Contraindications Documented hypersensitivity, heart block, sinus bradycardia
Interactions Rifampin, cisplatin, vinblastine, bleomycin, folic acid, theophylline, and continuous NG feedings may decrease serum levels and effects; may decrease effects of oral contraceptives, itraconazole, mebendazole, methadone, oral midazolam, valproic acid, cyclosporine, theophylline, doxycycline, quinidine, mexiletine, and disopyramide; isoniazid, chloramphenicol, or fluconazole may increase serum concentrations; may increase warfarin effects and rate of conversion of primidone to phenobarbital, resulting in increased phenobarbital serum concentrations
Pregnancy D - Unsafe in pregnancy
Precautions Discontinue if rash or lymphadenopathy develop; use caution in patients with hepatic dysfunction; phenytoin is about 90% protein bound—during pregnancy or low albumin states, better to adjust PO dose to maintain free serum concentrations of 1-2 mg/L
Drug Name
 
Lamotrigine (Lamictal) -- Triazine derivative useful in treatment of neuralgia. Inhibits release of glutamate and inhibits voltage-sensitive sodium channels, which stabilizes neuronal membrane. Follow manufacturer's recommendation for dose adjustments.
Adult Dose Monotherapy: 50-100 mg/d PO divided bid initial dose; maintenance: 100-400 mg/d qd or divided bid; not to exceed 500 mg/d Adjunct therapy with valproic acid: 25 mg PO qod initial dose; maintenance: 50-200 mg/d qd or divided bid; not to exceed 200 mg/d
Pediatric Dose 2-12 years Monotherapy: Weeks 1-2: 0.6 mg/kg/d PO divided bid, rounded down to the nearest 5 mg Weeks 3-4: 1.2 mg/kg/d PO divided bid, rounded down to the nearest 5 mg Maintenance: 5-15 mg/kg/d PO; not to exceed 400 mg/d divided bid; to achieve usual maintenance dose, increase subsequent doses q1-2wk as follows: Calculate 1.2 mg/kg/d and round down to nearest 5 mg; add this amount to previously administered daily dose
Concomitant therapy with valproic acid: Weeks 1-2: 0.15 mg/kg/d PO qd or divided bid, rounded down to nearest 5 mg; if initial calculated daily dose is 2.5-5 mg, then take 5 mg on alternate days for first 2 wk Weeks 3-4: 0.3 mg/kg/d PO qd or divided bid, rounded down to nearest 5 mg Maintenance: 1-5 mg/kg/d PO; not to exceed 200 mg/d qd or divided bid; to achieve usual maintenance dose, increase subsequent doses q1-2wk as follows: Calculate 0.3 mg/kg/d and round down to nearest 5 mg; add this amount to previously administered qd dose
>12 years Monotherapy: Weeks 1-2: 50 mg/d PO Weeks 3-4: 100 mg/d PO divided bid Maintenance: 300-500 mg/d PO divided bid; to achieve maintenance, increase by 100 mg/d q1-2wk
Concomitant therapy with valproic acid: Weeks 1-2: 25 mg PO qod Weeks 3-4: 25 mg PO qd Maintenance: 100-400 mg/d PO qd or divided bid; to achieve maintenance, increase by 25-50 mg/d q1-2wk
Contraindications Documented hypersensitivity
Interactions Acetaminophen increases renal clearance, decreasing effects; phenobarbital and phenytoin increase metabolism, causing decrease in lamotrigine levels; concomitant valproic acid increases half-life of lamotrigine
Pregnancy C - Safety for use during pregnancy has not been established.
Precautions Use caution in patients with impaired renal or hepatic function
  MISCELLANEOUS Section 8 of 9   Click here to go to the previous section in this topic Click here to go to the top of this page Click here to go to the next section in this topic
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Medical/Legal Pitfalls:

Trigeminal Neuralgia, aka Tic douloreaux  or  TN
&
Temporomandibular  Joint aka TMJ  Eventually Cancer.This website is about Brian Nelson's fight with a parotid (salivary) gland tumor. It started out with the symptoms of  Trigeminal Neuralgia, aka Tic douloreaux  or  TN & Temporomadibular Joint aka TMJ Click Here to see my other record file at IAmFightingCancer.com  Bookmark this page now!  
 
Scan down to read my very lengthy and detailed web journal. Call me if I can help you. 713-467-3025 Brian
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88
 
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Excerpt from Atypical Facial Pain

 

Please click here to view the full topic text: Atypical Facial Pain

Background: Atypical facial pain occurs in the territory of the trigeminal nerve, but the discomfort is not typical of trigeminal neuralgia. It may be as severe as trigeminal neuralgia, but its pattern and quality are different. Whereas trigeminal neuralgia is characterized by quick episodes of jabbing or lancinating pain, atypical facial pain is usually burning, aching, dull, or crushing. Moreover, an individual atypical facial pain attack always lasts longer than a few seconds and usually lasts minutes or hours (if not continuous). The distinction is important for making treatment decisions, because surgery, usually rhizotomy or vascular decompression, is highly effective for trigeminal neuralgia, whereas surgery is not appropriate for atypical facial pain.

A variation of atypical facial pain is discomfort similar to that of trigeminal neuralgia (eg, lancinating) but atypical in location (eg, far lateral on the face or in the occipital area). Some writers classify these as neuralgias of other nerves (in these examples, superficial temporal or occipital).

 

Frequency:
 

  • In the US: Although accurate figures are not possible because of the lack of agreement on criteria for classification, atypical facial pain is approximately one fifth as frequent as trigeminal neuralgia. The incidence of trigeminal neuralgia is 4-5 per 100,000 per year.

Race: No racial predilection is known.

Sex: Atypical facial pain affects both sexes with approximately equal frequency.

Age: The disorder mainly affects adults and is rare in the young.

Please click here to view the full topic text: Atypical Facial Pain

89TMJ Site 
90 Myelin  From http://www.miracosta.cc.ca.us/home/sfoster/neurons/mylen.htm  
The breakdown of the Myelin sheath is what causes you  to feel pain. This is caused by the blood vessel sitting on top of the nerve which is covered by the Myelin sheath  Listen to the audio clip on the Myelin Sheath .

                                       Myelin Sheath

The myelin sheath is the insulating coating of neuron made up largely of fat. It covers each axon. Because myelin is slippery and wet it increases the speed at which the electrical impulse is carried, thus increasing the velocity of nerve impulse. (See Node of Ranvier). Myelin covers some but not all vertebrate axons. Axons that are myelinated appear white and are therefore referred to as "white matter" (as opposed to "grey matter") in the central nervous system. Glossary
AUDIO

91 TNA  TRIGEMINAL NEURALGIA SITE MAP FOR TN.

 

 

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Trigeminal Neuralgia, aka Tic douloreaux  or  TN
&
Temporomandibular  Joint aka TMJ  Eventually Cancer.This website is about Brian Nelson's fight with a parotid (salivary) gland tumor. It started out with the symptoms of  Trigeminal Neuralgia, aka Tic douloreaux  or  TN & Temporomadibular Joint aka TMJ Click Here to see my other record file at IAmFightingCancer.com  Bookmark this page now!  
 
Scan down to read my very lengthy and detailed web journal. Call me if I can help you. 713-467-3025 Brian
Signature Card For:                 Brian Nelson    31 Gessner Rd. , Houston, TX  77024
Tel. 713-467-3025 (Refers to my cell)      Fax 713-467-3192        
Click here to e-mail me.

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92   What is a PET scan?

        A PET scan, or Positron Emission Tomography scan, is an imaging technique that allows physicians to examine many organs of the body and is helpful in diagnosing many diseases, such as cancer.  Other techniques, such as CT scan or MRI, only show organ structure, where as PET shows organ structure and function.  

PET is able to differentiate between malignant and benign tumors since it shows how the organ functions. PET can detect if a disease has moved from one part of the body to another, which is not evident clinically or through routine imaging.  By uncovering abnormalities that might otherwise go undetected, PET guides physicians to the most appropriate treatment.  

What’s involved in the procedure?

           During a PET scan, a patient receives an injection of a small amount of radioactive glucose (sugar) into their bloodstream.  There is no danger from this injection.  The radiation exposure associated with PET is similar to that of conventional CT scanning.  Next, the patient will wait about an hour while the injection is distributed through their body.  Then the patient will lie on a table, keeping their head still, that will slowly pass through the scanner. 

            The entire visit lasts about two to three hours.  The actual procedure is safe with no side effects, and lasts about forty-five minutes.  Typically, the patient will be asked not to eat or drink anything after midnight the night before their appointment.

Why are PET scans important when it comes to cancer?

Ø      Detects recurrent cancer early on.

Ø      Detects extremely small cancerous tumors, which means earlier diagnoses and treatment.

Ø      Differentiates between benign and malignant tumors.

Ø      Accurate in determining tumor stage.

Ø      Differentiates between operable and inoperable disease.

Ø      Non-invasive way of screening diseases.

Ø      Replaces multiple medical testing procedures with a single exam, producing imaging information of superior quality.

Ø      Can reduce or eliminate ineffective and unnecessary treatment - and the associated costs.

What Types of Diseases Can a PET Scan Detect?

The new Medicare Policy covers the following six cancer groups and also covers two non-cancer clinical conditions:

1. Lung Cancer
a) Solitary Pulmonary Nodule
b) Pathologically proven non-small cell lung cancer (NSCCa)

*Diagnosis, **Staging and Re-staging

2. Esophageal Cancer

*Diagnosis, **Staging, ***Re-staging

3. Colorectal Cancer

*Diagnosis, **Staging, and ***Re-staging

4. Lymphoma
a) Hodgkin's Disease
b) Non-Hodgkin's Lymphoma

*Diagnosis, **Staging, and ***Re-staging

5. Melanoma

*Diagnosis, **Staging, and ***Re-staging
-Not covered for evaluating regional lymph nodes

6. Head and Neck Cancer (excluding CNS and Thyroid)

*Diagnosis, **Staging, and ***Re-Staging

7. Breast Cancer

1) Staging of patients with distant metastases or restaging patients with locoregional recurrence or metastases.
2) Monitoring tumor response to therapy for women with locally advanced breast carcinoma.

8. Myocardial Variability

1) Primary or initial diagnostic study for assessing myocardial viability prior to vascularization

2) ****Covered following inconclusive SPECT

9. Medically Refractory Seizures

**Covered for pre-surgical evaluation

 
93
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The Merck Manual of Diagnosis and Therapy   hyperlink to list of sections
Section 14. Neurologic Disorders   hyperlink to list of chapters in current section
Chapter 178. Neuro-Ophthalmologic And Cranial Nerve Disorders
Topics
[General]
Neuro-Ophthalmologic Disorders
Cranial Nerve Disorders
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Cranial Nerve Disorders

The cranial nerves (except for the olfactory, optic, and part of the spinal accessory) leave the CNS from the brain stem (see Table 178-2). Their motor nuclei lie deep within the brain stem; their sensory nuclei, in ganglia just outside it.

THIRD CRANIAL NERVE PALSIES

Partial to complete weakness of the muscles innervated by the 3rd (oculomotor) nerve, resulting in ptosis of the lid, mydriasis, and an outwardly turned eye during primary gaze.

When the patient attempts to turn the eye inward, it moves slowly only to the midline. Upward and downward gaze is compromised in the affected eye. When downward gaze is attempted, the superior oblique muscle causes the eye to rotate inward.

The many causes of 3rd cranial nerve palsies include most major causes of CNS disease, so choice of diagnostic tests should be based on the clinical features of the palsy. Intraorbital structural lesions producing external ophthalmoplegia and ocular myopathies should be distinguished from cranial nerve disease. Exophthalmos or enophthalmos, a history of severe orbital trauma, or an obviously inflamed orbit suggests restrictive orbital disease, which may impair ocular motility. Myopathies are harder to diagnose but are suggested by a partial 3rd nerve palsy. The pupil is always spared in myopathy.

Completely nonfunctional parasympathetic fibers (causing fixed dilated pupils) strongly suggest oculomotor nerve compression. The most common causes are aneurysm (especially of the posterior communicating artery), trauma, and intracranial mass lesion. Oculomotor paralysis in an increasingly unresponsive patient suggests transtentorial herniation and is a major emergency. If the pupil is completely spared but all other muscles innervated by the 3rd nerve are affected (eg, diabetic 3rd nerve paresis), the cause is likely to be an ischemic process of the oculomotor nerve or the midbrain; a demyelinating process is less likely. However, about 5% of posterior communicating artery aneurysms causing oculomotor paralysis spare the pupil.

Third cranial nerve palsies are most indicative of serious disease when associated with severe headache or altered consciousness.

A thorough neurologic examination with CT or MRI is performed. Lumbar puncture is reserved for suspected subarachnoid hemorrhage when CT does not show blood. Cerebral angiography must be performed if aneurysm causing subarachnoid hemorrhage is strongly suspected or when the pupil is clearly affected and no head trauma serious enough to fracture the skull has occurred.

FOURTH CRANIAL NERVE PALSIES

Weakness of the muscle innervated by the 4th (trochlear) nerve (superior oblique muscle).

These palsies are often difficult to detect because they affect vertical eye position predominantly when the eye is turned inward. The patient sees double images, one above and slightly to the side of the other. However, by tilting the head to the side opposite the palsied muscle, the patient may achieve full or almost full ocular motility without double vision.

There are few common identified causes of 4th cranial nerve palsies; many are idiopathic. Closed head trauma without skull fracture is a common cause of unilateral and bilateral palsies; the few cases that occur often follow motor cycle accidents. Aneurysms, tumors, and multiple sclerosis are rare causes.

Evaluation of 4th nerve palsies is similar to that of 3rd nerve palsies. Usually, the diagnosis is obvious from the history and physical examination. Oculomotor exercises may help. Sometimes surgery is necessary to restore concordant vision.

SIXTH CRANIAL NERVE PALSIES

Weakness of the muscles innervated by the 6th (abducens) nerve.

The eye is turned inward; it moves outward sluggishly, reaching the midline at most.

Idiopathic cases are common, although many occur in elderly or diabetic patients in whom small vessel disease may be suspected. In idiopathic cases, no other cranial nerves are involved, and improvement should occur within 2 mo.

One identifiable cause is compression of the 6th nerve in the cavernous sinus by a tumor originating in the nasopharynx. Typically, severe pain in the head and anesthesia in the distribution of the first division of the 5th nerve also occur. Anything that causes the brain to shift may stretch the 6th nerve because of the acute angle it makes before entering Dorello's canal. Thus 6th nerve palsies may be due to large brain tumors remote from the nerve, to increased intracranial pressure, or to lumbar puncture. Diabetic infarction is one of the more common causes. Other causes include trauma of insufficient force to cause a basilar skull fracture, infections or tumors affecting the meninges, Wernicke's encephalopathy, aneurysm, and multiple sclerosis. In children without evidence of increased intracranial pressure, these palsies can result from respiratory infection and thus may be recurrent.

Diagnosing complete 6th cranial nerve palsies is easy, but determining their etiology can be more challenging. Excluding increased intracranial pressure and papilledema (by looking for retinal venous pulsations during funduscopy) is important. MRI or CT can help exclude intracranial mass lesions, hydrocephalus, and direct nerve compression by lesions in the orbit, cavernous sinus, and base of the skull. Lumbar puncture determines the CSF opening pressure and can detect leptomeningeal inflammatory, infectious, or neoplastic infiltrates entrapping the 6th nerve. A collagen vascular screen helps exclude a vasculopathic process. In many cases, 6th nerve palsies resolve once the primary disorder is treated.

TRIGEMINAL NEURALGIA
(Tic Douloureux)

A disorder of the trigeminal nerve producing bouts of excruciating, lancinating pain, lasting between seconds and 2 min, along the distribution of one or more of its sensory divisions, most often the maxillary.

At surgery or autopsy, intracranial arterial and, less often, venous loops compressing the trigeminal nerve root where it enters the brain stem have been found, suggesting that the tic is a compressive neuropathy. The disorder usually affects adults, especially the elderly. Pain is often set off by touching a trigger point or by activity (eg, chewing or brushing the teeth). Although each bout of intense pain is brief, successive bouts may be incapacitating.

Diagnosis

Usually, the history is typical and diagnostic. No clinical or pathologic signs accompany trigeminal neuralgia, so finding a sensory or cranial nerve abnormality requires search for a structural cause of the pain, such as a neoplasm, a multiple sclerosis plaque, or another lesion impinging on the nerve or its pathways in the brain stem. Pontine lesions usually result in sensory and motor dysfunction; a medullary lesion causes only sensory loss of pain and temperature with loss of the corneal reflex. Differential diagnosis includes neoplasm, vascular malformation of the brain stem, a vascular insult, and multiple sclerosis (especially in a younger patient). Postherpetic pain is differentiated by its typical antecedent rash, scarring, and predilection for the ophthalmic division. Trigeminal neuropathy may occur in Sjögren's syndrome or RA, but with a sensory deficit that is often perioral and nasal. Migraine may produce atypical facial pain, with normal examination results, but the pain is more prolonged and is burning or throbbing.

Treatment

Carbamazepine 200 mg 3 or 4 times a day is generally effective, and the benefit is often sustained; liver and hematopoietic functions should be monitored. If carbamazepine is ineffective or produces a toxic reaction, other options include phenytoin 300 to 600 mg/day, baclofen 30 to 80 mg/day, or amitriptyline 25 to 200 mg/day taken at bedtime. Peripheral nerve block provides temporary relief. In resistant cases, a craniectomy is performed to separate pulsating vascular structures (especially arteries) from the trigeminal root in the posterior fossa (Jannetta procedure). Electrolytic, chemical, or balloon-compressive lesions of the gasserian ganglion can be made via a percutaneous stereotaxically positioned needle. Occasionally, a last resort to relieve intractable pain is resection of the 5th nerve fibers between the gasserian ganglion and the brain stem.

FACIAL NERVE DISORDERS

Unilateral facial weakness is a common neurologic sign.

Bell's Palsy

Unilateral facial paralysis of sudden onset and unknown cause.

The mechanism presumably involves swelling of the nerve due to immune or viral disease, with ischemia and compression of the facial nerve in the narrow confines of its course through the temporal bone.

Pain behind the ear may precede facial weakness. Weakness develops within hours, sometimes to complete paralysis. The affected side becomes flat and expressionless, but patients may complain instead about the seemingly twisted intact side. In severe cases, the palpebral fissure widens, and the eye does not close. The patient may complain of a numb or heavy feeling in the face, but no sensory loss is demonstrable. A proximal lesion may affect salivation, taste, and lacrimation and may cause hyperacusis.

Diagnosis

Weakness of the entire half of the face distinguishes Bell's palsy from supranuclear lesions (eg, stroke, cerebral tumor), in which the weakness is partial, affecting the frontalis and orbicularis oculi less than the muscles in the lower part of the face. Bell's palsy must be differentiated from unilateral facial weakness due to other disorders of the facial nerve or its nucleus, chiefly geniculate herpes (Ramsay Hunt's syndrome), middle ear or mastoid infections, sarcoidosis, Lyme disease, petrous bone fractures, carcinomatous or leukemic nerve invasion, chronic meningeal infections, and cerebellopontine angle or glomus jugulare tumors. Skull x-rays and CT and MRI scans are obtained when the diagnosis is in doubt. MRI may show contrast enhancement of the facial nerve, but CT and skull x-rays are typically negative. However, they may show a fracture line, bony erosion due to infection or neoplasm, or internal auditory canal expansion due to a cerebellopontine angle tumor. CT and MRI scans may show the contrast-enhancing mass of angle or glomus tumors. Blood tests for Lyme disease help diagnose it. A chest x-ray and serum ACE are used to detect sarcoidosis, a common cause of facial nerve paralysis in blacks.

Prognosis and Treatment

The extent of nerve damage determines outcome; nerve conduction studies and electromyography are useful. Complete recovery within several months invariably follows acute partial paralysis. The likelihood of complete recovery after total paralysis is 90% if the nerve branches in the face retain normal excitability to supramaximal electrical stimulation but is only about 20% if electrical excitability is absent.

Misdirected regrowth of nerve fibers may innervate lower facial muscles with periocular fibers and vice versa, resulting in contraction of unexpected muscles during voluntary facial movements (synkinesia) or "crocodile tears" during salivation. Facial muscle contractures may follow chronic weakness.

Measures must be taken to prevent corneal drying. They include frequent use of natural tears, isotonic saline and methylcellulose drops, and strips of skin tape to help close the eye. Supportive measures, such as temporary patching, may suffice to protect the exposed eye; tarsorrhaphy may be needed when palpebral fissure persists.

Some studies suggest that corticosteroids (eg, prednisone 60 to 80 mg/day po begun 24 to 48 h after onset and given for 1 wk, then decreased gradually over the 2nd wk) help modestly reduce residual paralysis and expedite recovery. Mild electrical stimulation of the nerve and massage of the facial muscles have no proven benefit. Hypoglossal-facial nerve anastomosis may partially restore facial function if none has returned in 6 to 12 mo but results in difficulty in eating and speaking, so its role is limited.

GLOSSOPHARYNGEAL NEURALGIA

A rare syndrome characterized by recurrent attacks of severe pain in the posterior pharynx, tonsils, back of the tongue, and middle ear.

The cause is unknown, and no pathologic change can be found (except rarely, when due to a tumor in the cerebellopontine angle or the neck). Men are more commonly affected, usually after age 40.

As in trigeminal neuralgia, intermittent attacks of brief, severe, excruciating pain occur paroxysmally, either spontaneously or precipitated by movement (eg, chewing, swallowing, talking, sneezing). The pain, lasting seconds to a few minutes, usually begins in the tonsillar region or at the base of the tongue and may radiate to the ipsilateral ear. The pain is strictly unilateral. In 1 to 2% of patients, increased vagus nerve activity causes cardiac sinus arrest with syncope. Attacks may be separated by long intervals.

Diagnosis and Treatment

Location of the pain, precipitation of an attack by swallowing or by touching the tonsils with an applicator, and temporary elimination of pain with lidocaine applied locally to the throat (after which the pain cannot be evoked by stimulation) distinguish glossopharyngeal neuralgia from trigeminal neuralgia of the mandibular division. Tonsillar, pharyngeal, and cerebellopontine angle tumors and metastatic lesions in the anterior cervical triangle must be ruled out by brain imaging.

Carbamazepine is the drug of choice. Phenytoin, baclofen, or amitriptyline in doses as for trigeminal neuralgia (see above) or trazodone 150 to 400 mg/day in 3 divided doses may be added if necessary. If they are ineffective, cocainization of the pharynx may provide temporary relief, and surgery may be necessary. When pain is restricted to the pharynx, the nerve in the neck may be avulsed; it must be sectioned intracranially if pain is widespread.

94    CYMBALTA?

 

Has anyone tried taking the prescription medication called Cymbalta for TN or related facial pain?  If so, please let Shelly know about your experience.  Send an e-mail to Shelly at swilson@tna-support.org or write a note to Shelly Wilson at 604 Aberdeen Way, Southlake, TX  76092.

 

Cymbalta works to treat more than one condition.  Not only has Cymbalta been proven effective in treating depression, including both its emotional symptoms (such as sadness and irritability) and its physical symptoms (such as fatigue or vague aches and pains), it has also been proven effective managing the pain of diabetic peripheral neuropathy pain (DPNP). 

 

It is believed that Cymbalta acts as an antidepressant and pain reducer due to its effect on two naturally occurring chemicals in the brain and body, serotonin and norepinephrine.

 

Cymbalta comes in a capsule and can be taken once a day.  The recommended daily dose for Cymbalta is 60 mg.  However, your doctor may prescribe a different dose based on his or her medical judgment.  Cymbalta is available in 20 mg, 30 mg, and 60 mg capsules.  Cymbalta is not recommended for those under 18.  Cymbalta is not a narcotic.

 

Source:  www.cymbalta.com/

95

COMPUTER CHAT ROOM

 

Tracy Knight, a Trigeminal Neuralgia Association Telephone Support Contact, voluntarily takes phone calls from TN patients and their supporters at 972-617-7809.  She also donates her time to run a Yahoo! Group called TexasTNsupport.  This group is made for those who suffer from TN or have a loved one that suffers from TN and lives in the Texas area.

 

To visit this chat room, go to:  http://health.groups.yahoo.com/group/TexasTNsupport/

 

Thanks to Tracy for the time she gives our association!

96 DO YOU HAVE ANESTHESIA DOLOROSA?

 

We are compiling a list of facial pain patients that have anesthesia dolorosa so they can network with each other to learn what has helped relieve the pain.

 

As defined in the book “Striking Back!  The Trigeminal Neuralgia and Face Pain Handbook”, anesthesia dolorosa is a troubling and hard-to-treat combination of pain and numbness.

 

If you have anesthesia dolorosa and want to share your experience with other Texans suffering from with the same problem, please send an e-mail to Shelly Wilson at swilson@tna-support.org or send a written note to Shelly Wilson at 604 Aberdeen Way, Southlake, TX  76092.  Please state that it is OK for TNA to share your name, phone number, and e-mail address (if you have one) with other anesthesia dolorosa patients.

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Trigeminal Neuralgia, aka Tic douloreaux  or  TN
&
Temporomandibular  Joint aka TMJ  Eventually Cancer.This website is about Brian Nelson's fight with a parotid (salivary) gland tumor. It started out with the symptoms of  Trigeminal Neuralgia, aka Tic douloreaux  or  TN & Temporomadibular Joint aka TMJ Click Here to see my other record file at IAmFightingCancer.com  Bookmark this page now!  
 
Scan down to read my very lengthy and detailed web journal. Call me if I can help you. 713-467-3025 Brian
Signature Card For:                 Brian Nelson    31 Gessner Rd. , Houston, TX  77024
Tel. 713-467-3025 (Refers to my cell)      Fax 713-467-3192        
Click here to e-mail me.

www.NelsonIdeas.com
       Make a difference in the world!  "Idea Possibility Consulting"
www.BrianNelsonConsulting.com    There are so many new ways to make more profit. 
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09/06/2006 12:11 PM -0500
31 Gessner Rd. Houston, TX  77024

Tel. 713-467-3025, Fax 713-467-3192 Click: E-mail me Updated 09/06/2006 12:11 PM -0500
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