Trigeminal Neuralgia: Difference between revisions

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'''Lead Editors'''    
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<br>
 
== Introduction ==
 
Trigeminal Neuralgia (TN), also known as "Tic D", is afacial pain syndrome. It is characterized by unilateral facial pain following the sensory distribution of cranial nerve V, the Trigeminal Nerve. Most commonly the pain radiates to the mandibular or maxillary regions (in 35% of paitients). In some cases it is accompanied by a brief facial spasm or tic.
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== Clinically Relevant Anatomy<br>  ==
== Clinically Relevant Anatomy<br>  ==


add text here relating to '''''clinically relevant''''' anatomy of the condition<br>  
The trigeminal nerve (the fifth cranial nerve, or simply CN V) is the nerve responsible for sensation in the face, and control of motor functions such as biting and chewing.
 
&nbsp;Its name ("trigeminal" = tri- or three, and -geminus or twin, or thrice twinned) derives from the fact that it has three major branches: the ophthalmic nerve (V1) 1st branch; the maxillary nerve (V2) 2nd branch, and the mandibular nerve (V3) 3rd branch. The ophthalmic and maxillary nerves are purely sensory. The mandibular nerve has both cutaneous and motor functions, the motor supply being tothe muscles of mastication. which include temporalis and masseter.<br>  
 
[[Image:Trigeminal_Nerve_Gray778_.png|400px|Trigeminal Nerve shown in yellow]]&nbsp;[[Image:Trigeminal_Branches.gif]]


== Mechanism of Injury / Pathological Process<br>  ==
== Mechanism of Injury / Pathological Process<br>  ==


add text here relating to the mechanism of injury and/or pathology of the condition<br>  
Usually, no structural lesion is present (85%), although many investigators agree that vascular compression (,ie. venous or arterial loops at the trigeminal nerve entry into the pons) is implicated in the pathogenesis of the idiopathic variety. This compression results in focal trigeminal nerve demyelination. The etiology is labeled idiopathic by default, and is then categorized as "classic trigeminal neuralgia"
 
Microanatomic small and large fibre damage in the nerve, essentially demyelination <ref>Burchiel KJ. Abnormal impulse generation in focally demyelinated trigeminal roots. J Neurosurg. Nov 1980;53(5):674-83</ref>&nbsp;leads to ephaptic transmission, in which action potentials jump from one fiber to another.
 
== Epidemiology ==
 
Recent estimates suggest the prevalence is approximately 1.5 cases per 10,000 population, with an incidence of approximately 15,000 cases per year.
 
==== Age ====
 
In 90% of patients, the disease begins after age 40 years, most often between 60-70 years.
 
==== Gender ====
 
Woman are &nbsp;affected more than men, with figures quoted between&nbsp; 3:2 to 2:1.&nbsp;
 
==== Multiple Sclerosis ====
 
Rushton and Olafson found that approximately 1% of patients with multiple sclerosis (MS) develop TN<ref>Rushton JG, Olafson RA. Trigeminal neuralgia associated with multiple sclerosis. A case report. Arch Neurol. Oct 1965;13(4):383-6</ref>,
 
Jensen et al noted that 2% of patients with trigeminal neuralgia have multiple sclerosis<ref>Jensen TS, Rasmussen P, Reske-Nielsen E. Association of trigeminal neuralgia with multiple sclerosis: clinical and pathological features. Acta Neurol Scand. Mar 1982;65(3):182-9</ref>
 
Patients with both conditions frequently have bilateral trigeminal neuralgia.


== Clinical Presentation  ==
== Clinical Presentation  ==


add text here relating to the clinical presentation of the condition<br>  
Trigeminal neuralgia (TN) presents as a stabbing unilateral facial pain that is usually triggered by chewing activities, or by touching affected areas on the face. <br>  


== Diagnostic Procedures  ==
==== Area of pain ====


add text here relating to diagnostic tests for the condition<br>  
60% of patients with TN present with lancinating pain shooting from the corner of the mouth to the angle of the jaw
 
30% experience jolts of pain from the upper lip or canine teeth to the eye and eyebrow, sparing the orbit itself—this distribution falls between the division of the first and second portions of the nerve.
 
According to Patten<ref>Patten J. Trigeminal neuralgia. In: Neurological Differential Diagnosis. 2nd ed. London: Springer;1996:373-5.</ref>, fewer than 5% of patients experience ophthalmic branch involvement.
 
==== Characteristic Descriptors of pain ====
 
The pain quality is &nbsp;severe, paroxysmal, and lancinating.
 
It usually starts with a sensation of electrical shocks, then quickly increases in less than 20 seconds to an excruciating discomfort felt deep in the face, often contorting the patient's expression. The pain then begins to fade within seconds, only to give way to a burning ache lasting seconds to minutes. During attacks, patients may grimace, wince, or make an aversive head movement, as if trying to escape the pain, thus producing an obvious movement, or tic; hence the term "tic douloureux."
 
==== Fquency of pain ====
 
The number of attacks may vary from less than 1 per day, to hundreds per day.
 
Outbursts fully abate between attacks, even when they are severe and frequent.
 
==== Pain Triggers ====
 
A common feature of TN is that the pain is triggered by touching the painful area of the face, as well as activities such as shaving, rubbing, brushing teeth, moving face to talk, cold wind on the face, etc.
 
Studies suggest that&nbsp; trigger zones, or areas of increased sensitivity, are present in one half of patients and often lie near the nose or mouth<ref>Sands GH. Pain in the face. Headaches in Adults, Annual Course, American Academy of Neurology Annual Meeting. 1994;3:146:130-2</ref>.
 
== Diagnosis and Classification ==
 
The International Headache Society (IHS) have published strict criteria<ref>The International Classification of Headache Disorders: 2nd edition. Cephalalgia. 2004;24 Suppl 1:9-160</ref> for TN:
 
A - Paroxysmal attacks of pain lasting from a fraction of a second to 2 minutes, affecting 1 or more divisions of the trigeminal nerve and fulfilling criteria B and C<br>B - Pain has at least 1 of the following characteristics: (1) intense, sharp, superficial or stabbing; or (2) precipitated from trigger areas or by trigger factors<br>C - Attacks stereotyped in the individual patient<br>D - No clinically evident neurologic deficit<br>E - Not attributed to another disorder
 
No laboratory, electrophysiologic, or radiologic testing is routinely indicated for the diagnosis of trigeminal neuralgia (TN), as patients with characteristic history and normal neurologic examination may be treated without further investigation.
 
The diagnosis of TN is almost entirely based on the patient's history and in most cases &nbsp;no specific laboratory tests are needed.
 
MRI scanning is often indicated simply to exclude other causes of the pain, such as pressure on the trigeminal nerve from [[Acoustic_Neuroma|Acoustic Neuroma]].


== Outcome Measures  ==
== Outcome Measures  ==
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== Management / Interventions<br>  ==
== Management / Interventions<br>  ==


add text here relating to management approaches to the condition<br>  
==== Medical Management  ====
 
A range of anti-epileptic drugs have proved to be useful in management of TN, with carbamazepine in particular having a large number of studies demonstrating efficacy<ref>Rockliff BW, Davis EH. Controlled sequential trials of carbamazepine in trigeminal neuralgia. Arch Neurol. Aug 1966;15(2):129-36</ref>.
 
Non anti-epileptic drugs can also be prescribed, often in conjunction with carbamazepine<ref>He L, Wu B, Zhou M. Non-antiepileptic drugs for trigeminal neuralgia. Cochrane Database Syst Rev. Jul 19 2006;3:CD004029</ref>.
 
==== Surgical Management ====
 
Studies suggest that approximately 25% of TN patients go on to require surgery as their condition worsens over years, and the drug management becomes less effective<ref>Dalessio DJ. Trigeminal neuralgia. A practical approach to treatment. Drugs. Sep 1982;24(3):248-55</ref>.&nbsp; Microvascular decompression and radiofrequency thermorhizotomy are the most common surgical procedures employed in these cases.


== Differential Diagnosis<br>  ==
== Differential Diagnosis<br>  ==


add text here relating to the differential diagnosis of this condition<br>
The main diffential diagnoses for TN are:
 
*Atypical facial pain - this common facial pain is less intense than TN, described as a dull or throbbing ache which lasts for minutes to hours
*[[Migraine_Headache|Migraine]] can cause severe unilateral facial pain
*As can [[Cluster_Headaches|Cluster headaches]]


== Key Evidence  ==
== Key Evidence  ==
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== Recent Related Research (from [http://www.ncbi.nlm.nih.gov/pubmed/ Pubmed])  ==
== Recent Related Research (from [http://www.ncbi.nlm.nih.gov/pubmed/ Pubmed])  ==
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<rss>Feed goes here!!|charset=UTF-8|short|max=10</rss>  
<rss>http://www.ncbi.nlm.nih.gov/entrez/eutils/erss.cgi?rss_guid=1LM5GtZJjqwO8IlOMFGBSud01Y8ODHi5mAbs9kHjHz6Jw78UcD|charset=UTF-8|short|max=10</rss>  
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== References  ==
== References  ==
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References will automatically be added here, see [[Adding References|adding references tutorial]].  
References will automatically be added here, see [[Adding References|adding references tutorial]].  


<references />
<references /> &nbsp;  
&nbsp;
 
[[Category:Neurology]]

Revision as of 01:21, 27 April 2014

Original Editor - Your name will be added here if you created the original content for this page.

Lead Editors  


Introduction[edit | edit source]

Trigeminal Neuralgia (TN), also known as "Tic D", is afacial pain syndrome. It is characterized by unilateral facial pain following the sensory distribution of cranial nerve V, the Trigeminal Nerve. Most commonly the pain radiates to the mandibular or maxillary regions (in 35% of paitients). In some cases it is accompanied by a brief facial spasm or tic.

Clinically Relevant Anatomy
[edit | edit source]

The trigeminal nerve (the fifth cranial nerve, or simply CN V) is the nerve responsible for sensation in the face, and control of motor functions such as biting and chewing.

 Its name ("trigeminal" = tri- or three, and -geminus or twin, or thrice twinned) derives from the fact that it has three major branches: the ophthalmic nerve (V1) 1st branch; the maxillary nerve (V2) 2nd branch, and the mandibular nerve (V3) 3rd branch. The ophthalmic and maxillary nerves are purely sensory. The mandibular nerve has both cutaneous and motor functions, the motor supply being tothe muscles of mastication. which include temporalis and masseter.

Trigeminal Nerve shown in yellow Trigeminal Branches.gif

Mechanism of Injury / Pathological Process
[edit | edit source]

Usually, no structural lesion is present (85%), although many investigators agree that vascular compression (,ie. venous or arterial loops at the trigeminal nerve entry into the pons) is implicated in the pathogenesis of the idiopathic variety. This compression results in focal trigeminal nerve demyelination. The etiology is labeled idiopathic by default, and is then categorized as "classic trigeminal neuralgia"

Microanatomic small and large fibre damage in the nerve, essentially demyelination [1] leads to ephaptic transmission, in which action potentials jump from one fiber to another.

Epidemiology[edit | edit source]

Recent estimates suggest the prevalence is approximately 1.5 cases per 10,000 population, with an incidence of approximately 15,000 cases per year.

Age[edit | edit source]

In 90% of patients, the disease begins after age 40 years, most often between 60-70 years.

Gender[edit | edit source]

Woman are  affected more than men, with figures quoted between  3:2 to 2:1. 

Multiple Sclerosis[edit | edit source]

Rushton and Olafson found that approximately 1% of patients with multiple sclerosis (MS) develop TN[2],

Jensen et al noted that 2% of patients with trigeminal neuralgia have multiple sclerosis[3]

Patients with both conditions frequently have bilateral trigeminal neuralgia.

Clinical Presentation[edit | edit source]

Trigeminal neuralgia (TN) presents as a stabbing unilateral facial pain that is usually triggered by chewing activities, or by touching affected areas on the face.

Area of pain[edit | edit source]

60% of patients with TN present with lancinating pain shooting from the corner of the mouth to the angle of the jaw

30% experience jolts of pain from the upper lip or canine teeth to the eye and eyebrow, sparing the orbit itself—this distribution falls between the division of the first and second portions of the nerve.

According to Patten[4], fewer than 5% of patients experience ophthalmic branch involvement.

Characteristic Descriptors of pain[edit | edit source]

The pain quality is  severe, paroxysmal, and lancinating.

It usually starts with a sensation of electrical shocks, then quickly increases in less than 20 seconds to an excruciating discomfort felt deep in the face, often contorting the patient's expression. The pain then begins to fade within seconds, only to give way to a burning ache lasting seconds to minutes. During attacks, patients may grimace, wince, or make an aversive head movement, as if trying to escape the pain, thus producing an obvious movement, or tic; hence the term "tic douloureux."

Fquency of pain[edit | edit source]

The number of attacks may vary from less than 1 per day, to hundreds per day.

Outbursts fully abate between attacks, even when they are severe and frequent.

Pain Triggers[edit | edit source]

A common feature of TN is that the pain is triggered by touching the painful area of the face, as well as activities such as shaving, rubbing, brushing teeth, moving face to talk, cold wind on the face, etc.

Studies suggest that  trigger zones, or areas of increased sensitivity, are present in one half of patients and often lie near the nose or mouth[5].

Diagnosis and Classification[edit | edit source]

The International Headache Society (IHS) have published strict criteria[6] for TN:

A - Paroxysmal attacks of pain lasting from a fraction of a second to 2 minutes, affecting 1 or more divisions of the trigeminal nerve and fulfilling criteria B and C
B - Pain has at least 1 of the following characteristics: (1) intense, sharp, superficial or stabbing; or (2) precipitated from trigger areas or by trigger factors
C - Attacks stereotyped in the individual patient
D - No clinically evident neurologic deficit
E - Not attributed to another disorder

No laboratory, electrophysiologic, or radiologic testing is routinely indicated for the diagnosis of trigeminal neuralgia (TN), as patients with characteristic history and normal neurologic examination may be treated without further investigation.

The diagnosis of TN is almost entirely based on the patient's history and in most cases  no specific laboratory tests are needed.

MRI scanning is often indicated simply to exclude other causes of the pain, such as pressure on the trigeminal nerve from Acoustic Neuroma.

Outcome Measures[edit | edit source]

add links to outcome measures here (see Outcome Measures Database)

Management / Interventions
[edit | edit source]

Medical Management[edit | edit source]

A range of anti-epileptic drugs have proved to be useful in management of TN, with carbamazepine in particular having a large number of studies demonstrating efficacy[7].

Non anti-epileptic drugs can also be prescribed, often in conjunction with carbamazepine[8].

Surgical Management[edit | edit source]

Studies suggest that approximately 25% of TN patients go on to require surgery as their condition worsens over years, and the drug management becomes less effective[9].  Microvascular decompression and radiofrequency thermorhizotomy are the most common surgical procedures employed in these cases.

Differential Diagnosis
[edit | edit source]

The main diffential diagnoses for TN are:

  • Atypical facial pain - this common facial pain is less intense than TN, described as a dull or throbbing ache which lasts for minutes to hours
  • Migraine can cause severe unilateral facial pain
  • As can Cluster headaches

Key Evidence[edit | edit source]

add text here relating to key evidence with regards to any of the above headings

Resources
[edit | edit source]

add appropriate resources here

Case Studies[edit | edit source]

add links to case studies here (case studies should be added on new pages using the case study template)

Recent Related Research (from Pubmed)[edit | edit source]

Failed to load RSS feed from http://www.ncbi.nlm.nih.gov/entrez/eutils/erss.cgi?rss_guid=1LM5GtZJjqwO8IlOMFGBSud01Y8ODHi5mAbs9kHjHz6Jw78UcD|charset=UTF-8|short|max=10: Error parsing XML for RSS

References[edit | edit source]

References will automatically be added here, see adding references tutorial.

  1. Burchiel KJ. Abnormal impulse generation in focally demyelinated trigeminal roots. J Neurosurg. Nov 1980;53(5):674-83
  2. Rushton JG, Olafson RA. Trigeminal neuralgia associated with multiple sclerosis. A case report. Arch Neurol. Oct 1965;13(4):383-6
  3. Jensen TS, Rasmussen P, Reske-Nielsen E. Association of trigeminal neuralgia with multiple sclerosis: clinical and pathological features. Acta Neurol Scand. Mar 1982;65(3):182-9
  4. Patten J. Trigeminal neuralgia. In: Neurological Differential Diagnosis. 2nd ed. London: Springer;1996:373-5.
  5. Sands GH. Pain in the face. Headaches in Adults, Annual Course, American Academy of Neurology Annual Meeting. 1994;3:146:130-2
  6. The International Classification of Headache Disorders: 2nd edition. Cephalalgia. 2004;24 Suppl 1:9-160
  7. Rockliff BW, Davis EH. Controlled sequential trials of carbamazepine in trigeminal neuralgia. Arch Neurol. Aug 1966;15(2):129-36
  8. He L, Wu B, Zhou M. Non-antiepileptic drugs for trigeminal neuralgia. Cochrane Database Syst Rev. Jul 19 2006;3:CD004029
  9. Dalessio DJ. Trigeminal neuralgia. A practical approach to treatment. Drugs. Sep 1982;24(3):248-55