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PANKAJ KUMAR
BDS FINAL YEAR
ORAL AND MAXILOFACIAL SURGERY
CONTENTS
Introduction
Definition
Classification
Etiology and Pathogenesis
Clinical features
Diagnosis
Treatment and management
Public Health Importance
Conclusion
References
INTRODUCTION
Anatomy of Trigeminal nerve
DEFINITION
• Sudden, usually
unilateral, severe brief
stabbing pain in the
distribution of one of
more branches of the
V nerve.
Other names
Tic douloureux – Nicholaus Andre
Fothergill’s disease – John Fothergill
CLASSIFICATION:
International Headache Society (IHS) classified
trigeminal neuralgia into two types:
Classical /idiopathic/typical
Symptomatic
Classical trigeminal
neuralgia is a unilateral
disorder characterized
by brief electric, shock-
like pains.
are abrupt in
and termination
They
onset
and limited to the
distribution of one or
more divisions of the
trigeminal nerve.
Symptomatic trigeminal neuralgia
Pain is similar to classical type
But it is
structural
caused
lesion
by a
other
demonstrable
than vascular
compression.
ETIOLOGY
Compression of the trigeminal nerve root
Primary demyelination disorders
Multiple sclerosis
Charcot-Marie-Tooth disease(hereditary
sensory motor neuropathy)
Infiltrative disorders of the trigeminal nerve
root, ganglion and nerve
Carcinomatous deposits
Perineural spread of head and neck cancer
Non-demyelinating lesions of the pons or
medulla
Familial trigeminal neuralgia
Compression of the Trigeminal Nerve Root
Compressive lesions
Tumor of cerebellar pontine angle
Posterior cranial fossa tumors
Schwannomas
Meningioma
Epidermoid cyst
deformity
imperfecta
Compression from osteoma or
resulting from osteogenesis
(rarely)
PATHOGENESIS
Superior cerebellar artery pressing on or
grooving the root of the nerve causes pressure
which results in
focal demyelinization and hyperexcitability of
nerve fibres
which fire in response to light touch resulting in
brief episodes of intense pain.
CLINICAL FEATURES
Rare
Middle age
Female predilection (60%)
Maxillary division more commonly involved
Opthalmic division rarely involved
Shaving, showering, speaking, eating, or
exposure to wind triggers episodes
Contd…….
CLINICAL FEATURES……………….
Pain occurs in areas of the face where the
trigeminal nerve supplies normal sensation:
cheek, jaw, teeth, gums and lips, and
sometimes the eye or forehead
The pain is described as episodes of
–stabbing, electric
intense feeling like
shocks, burning, crushing, exploding,
lancenating pain
Pain lasts for few
seconds to minutes
Unilateral
(predominantly right
side)
Precipitated by trigger
zones
Extreme cases ‘frozen
or mask like face’
Trigger zones
DIAGNOSIS
 History
 Clinical examination
 Diagnostic LAblocks
 CT scan
 MRI
Pain History
 Chief complaint
 History of present illness
 Current symptoms: Onset, Location, Quality,
Intensity, Frequency, Duration
 Aggravating and alleviating factors
 Past treatments
IHS diagnostic criteria for trigeminal
neuralgia
Classic trigeminal neuralgia
A. Paroxysmal attacks of facial or frontal pain
that last a few seconds to less than 2 minutes,
affecting one or more divisions of the
trigeminal nerve and fulfilling criteria B and
C.
B. Pain has at least one of the following
characteristics:
1. Intense, sharp, superficial or stabbing
2.Precipitated from trigger areas or by
trigger factors
3.The patient is entirely asymptomatic
between paroxysms.
are stereotyped in the individual
no clinically evident neurological
C. Attacks
patient.
D. There is
deficit.
E. Not attributed to another disorder.
Symptomatic trigeminal neuralgia
A. Paroxysmal attacks of pain lasting from a
fraction of a second to 2 minutes, with or
without persistence of aching between
paroxysms, affecting one or more divisions of
the trigeminal nerve and fulfilling criteria B.
B. Pain has at least one of the following
characteristics:
1. Intense, sharp, superficial or stabbing
2.Precipitated from trigger areas orby trigger
factors
3.Attacks are stereotyped in the individual
patient
4. A causative lesion, other than vascular
compression, has been demonstrated by
special investigations and/or posterior fossa
exploration.
Differential Diagnosis Of Classic
Trigeminal Neuralgia
1. Secondary trigeminal neuralgia
2. Pain of dental origin
3. Extracranial
4. Neuropathic
5. Neurovascular
6. Psychogenic
TREATMENT
Medical management
Surgical management
Treatment of trigeminal neuralgia is broadly
divided into two categories:
1. Destructive treatment:
 Radiofrequency Rhizotomies
 Balloon Gangliolysis
 Stereotactic Radiosurgery (ie Gamma Knife)
The possible complication of destructive
treatment is facial numbness, neuroparalytic
keratitis, or the sever complication of anesthesia
dolorosa which is a more complex facial pain.
2. Non destructive treatment:
 Medical treatment (Tegretol, Baclofen,
Dilantin, etc.)
 Microvascular decompression (with initial
success rate of 85 to 95%)
The possible complication of non destructive
treatment is side effect of medication and risk of
surgery.
Medical management
CARBAMAZEPINE
100– 200mg, bd ortid
Which provides benefit to more than 75% of
patients
Common trade names: Tegretol, Tegretol XL,
Carbitrol
Mode of action
Side effects
Other Medication
 Oxcarbazepine
 Gabapentin
 Lamotrigine
 Baclofen
 Topiramate
 Sodium valproate
 Phenytoin
 Clonazepam
 Felbamate
 Pimozide
 Zonisamide
 Pregabalin
Surgical management
Surgical options have been reserved for those
patients
who have a clearly defined secondary cause
for the trigeminal neuralgia,
who are unresponsive,
who have severe, unremitting pain that
limits their ability to eat,
for whom multiple medications are
intolerable or contraindicated
Surgical options
Percutaneous glycerol rhizolysis
Percutaneous balloon compression
Radiofrequency trigeminal (retrogasserian)
rhizotomy
Gamma knife radiosurgery
Microvascular decompression
Percutaneous Glycerol Rhizolysis
This procedure is used in
Arterial or venous compression of the
trigeminal nerve
Multiple sclerosis
Done with absolute alcohol or
phenol/glycerol mixture injected
phenol or
into the
trigeminal cistern
Hartel technique
When the needle pierces the foramen ovale and enters
the trigeminal cistern there is usually a characteristic
jaw twitch and CSF returns through the needle.
Lack of CSF return may be related to poor position of
the needle or to scarring within the cistern due to prior
surgery
Glycerol rhizolysis (GR)
Test dose: 0.1-0.15 ml
0.05~0.1 ml at 3~5 min. intervals
Total dose: 0.1~0.4 ml
Sensory changes: pain, burning or
paresthesia
Percutaneous balloon compression
0.5 - 1ml of contrast
Pear-shape balloon
Compression time: 1-7
min.
Radiofrequency thermo-coagulation
 The theory behind the use of radiofrequency to
lesion the trigeminal nerve is that it may
selectively injures/destroys the unmyelinated
or poorly myelinated nociceptive nerve fibers
and spares the (heavily) myelinated fibers
which serve touch, proprioception, and motor
function
Apermanent lesion in the retrogasserian trigemianal
nerve is made by beginning at 10Vand approximately
60mAfor a duration of 30-40 sec and increasing to
approx. 20Vand 100mA
(a) Thermal lesion of trigeminal nerve. (b) Mislocation of the electrode
(c) Expansion of thermal energy to neighboring neural structures.
Gamma knife radiosurgery
 The Gamma
focused array
intercepting beams
Knife is a
of
201
of
gamma radiation, produced
by separate cobalt sources.
 The dose is 70–90Gy.
 Pain relief is usually not
immediate.
 The mean time to pain relief
in two series was
approximately one month.
Microvascular decompression
It is the only medical or surgical intervention
that directly addresses the presumed
underlying pathology of classic trigeminal
neuralgia.
Retrosigmoid craniectomy approach
Operative approach
Microvascular decompression(MVD)
RFL for patients who are elderly or medically
frail.
Posterior fossa exploration and MVD for
younger healthier patients who can tolerate the
longer more invasive surgical procedure.
GKR as an alternative to RFL in frail or elderly
patients. MVD or RFL remains the standard
for surgical treatment of younger patients who
have considerable life expectancy
Peripheral procedures
Peripheral
neurectomies
Cryotherapy
(cryonanlgesia)
Alcohol block
Streptomycin –
lidocaine injections
OMFS….
Peripheral neurectomy
Supra orbital
Infra orbital
Mental
Inferior alveolar
Long buccal
Lingual (rarely)
Infraorbital neurectomy
SUPRAORBITAL NEURECTOMY
Inferior Alveolar Nerve
Neurectomy
Trigeminal Neuralgia Diet
Low fat, high protein, high calorie
Easy chewable foods
Served lukewarm
Offered frequently
Trigeminal Neuralgia Association recommends
 avoidance of: extreme hot/cold, hot sauce,
chili, spicy salsa, mints, black pepper,
cinnamon, ginger, nutmeg
PUBLIC HEALTH IMPORTANCE
 Trigeminal neuralgia has an incidence of 4–5
per 100,000 of the
population.
 It is nearly twice as common in women,
 Incidence increases in age to around 1 in
1000 patients older than 75 years of
age.
 Rarely,familial cases have been reported.
 It is reported that 150,000 people are
diagnosed with trigeminal neuralgia every
year.
 The only indication about the prevalence of
TN comes from a study by Penman , who in
1969 reported rates of 107.5/1000000 in men
and 200.2/1000000 in women.
 TN is therefore a raredisease
 TN incidence progressively increases with
increasing age: from 17.5/100000/ between 60
and 69 years of age up to 25.6/100000/year
after 70.
 The female-to-male ratio was 1.74:1 in the
Katusic et al. study
 and 3:2 in another study by Ashkenazi and
Levin.
CONCLUSION
Population-based epidemiological studies
are essential to determine the spectrum of
TN symptoms in the population,
identifying individuals in whom symptoms
are mild enough that they do not seek
treatment. Potentially useful approaches in
studying the epidemiology of TN include
multi-site population-based studies
A concerted program of epidemiologic
to identify these key
studies is needed
features of TN: prevalence and public
health impact, especially among women
and members of minority groups; risk
factors; comorbidity; prodromal symptoms;
and natural history.
REFERENCES:
Fonseca, Marciani, Turvey, Oral and
Maxillofacial surgery, 2nd edition, volumeII
,Saunders Elsevier, 2009.
Jafferey P. Okeson, Bells Orofacial pain, 6th
edition, Quintessence publishing co Inc,
2005.
Peterson, Ellis, Hupp, Tucker, Oral and
maxillofacial surgery, 4th edition, Elsevier,
2003.
G.C. Manzoni , P. Torelli, Epidemiology of typical
and atypical craniofacial neuralgias, Neurol Sci
(2005) 26: S65–S67
Abhishek singh nayyar, Mubeen Khan, Trigeminal
Neuralgia: Revisiting clinical characteristics in the
Indian scenario. A Journal of Medical science and
Technology. Volume I, Issue 2, August 2012; pages
9-17
Cheryl A. Kitt et al., Topical review Trigeminal
neuralgia: opportunities for research and
treatment, International Association for the Study
of Pain, 2000.
THANK YOU

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Trigeminalneuralgiaseminar2 180526065218-converted

  • 2. CONTENTS Introduction Definition Classification Etiology and Pathogenesis Clinical features Diagnosis Treatment and management Public Health Importance Conclusion References
  • 4.
  • 5.
  • 6. DEFINITION • Sudden, usually unilateral, severe brief stabbing pain in the distribution of one of more branches of the V nerve.
  • 7. Other names Tic douloureux – Nicholaus Andre Fothergill’s disease – John Fothergill
  • 8. CLASSIFICATION: International Headache Society (IHS) classified trigeminal neuralgia into two types: Classical /idiopathic/typical Symptomatic
  • 9. Classical trigeminal neuralgia is a unilateral disorder characterized by brief electric, shock- like pains. are abrupt in and termination They onset and limited to the distribution of one or more divisions of the trigeminal nerve.
  • 10. Symptomatic trigeminal neuralgia Pain is similar to classical type But it is structural caused lesion by a other demonstrable than vascular compression.
  • 11. ETIOLOGY Compression of the trigeminal nerve root Primary demyelination disorders Multiple sclerosis Charcot-Marie-Tooth disease(hereditary sensory motor neuropathy) Infiltrative disorders of the trigeminal nerve root, ganglion and nerve Carcinomatous deposits Perineural spread of head and neck cancer Non-demyelinating lesions of the pons or medulla Familial trigeminal neuralgia
  • 12. Compression of the Trigeminal Nerve Root
  • 13.
  • 14. Compressive lesions Tumor of cerebellar pontine angle Posterior cranial fossa tumors Schwannomas Meningioma Epidermoid cyst deformity imperfecta Compression from osteoma or resulting from osteogenesis (rarely)
  • 15.
  • 16. PATHOGENESIS Superior cerebellar artery pressing on or grooving the root of the nerve causes pressure which results in focal demyelinization and hyperexcitability of nerve fibres which fire in response to light touch resulting in brief episodes of intense pain.
  • 17. CLINICAL FEATURES Rare Middle age Female predilection (60%) Maxillary division more commonly involved Opthalmic division rarely involved Shaving, showering, speaking, eating, or exposure to wind triggers episodes Contd…….
  • 18. CLINICAL FEATURES………………. Pain occurs in areas of the face where the trigeminal nerve supplies normal sensation: cheek, jaw, teeth, gums and lips, and sometimes the eye or forehead The pain is described as episodes of –stabbing, electric intense feeling like shocks, burning, crushing, exploding, lancenating pain
  • 19. Pain lasts for few seconds to minutes Unilateral (predominantly right side) Precipitated by trigger zones Extreme cases ‘frozen or mask like face’
  • 21.
  • 22. DIAGNOSIS  History  Clinical examination  Diagnostic LAblocks  CT scan  MRI
  • 23. Pain History  Chief complaint  History of present illness  Current symptoms: Onset, Location, Quality, Intensity, Frequency, Duration  Aggravating and alleviating factors  Past treatments
  • 24. IHS diagnostic criteria for trigeminal neuralgia Classic trigeminal neuralgia A. Paroxysmal attacks of facial or frontal pain that last a few seconds to less than 2 minutes, affecting one or more divisions of the trigeminal nerve and fulfilling criteria B and C.
  • 25. B. Pain has at least one of the following characteristics: 1. Intense, sharp, superficial or stabbing 2.Precipitated from trigger areas or by trigger factors 3.The patient is entirely asymptomatic between paroxysms.
  • 26. are stereotyped in the individual no clinically evident neurological C. Attacks patient. D. There is deficit. E. Not attributed to another disorder.
  • 27. Symptomatic trigeminal neuralgia A. Paroxysmal attacks of pain lasting from a fraction of a second to 2 minutes, with or without persistence of aching between paroxysms, affecting one or more divisions of the trigeminal nerve and fulfilling criteria B.
  • 28. B. Pain has at least one of the following characteristics: 1. Intense, sharp, superficial or stabbing 2.Precipitated from trigger areas orby trigger factors 3.Attacks are stereotyped in the individual patient 4. A causative lesion, other than vascular compression, has been demonstrated by special investigations and/or posterior fossa exploration.
  • 29. Differential Diagnosis Of Classic Trigeminal Neuralgia 1. Secondary trigeminal neuralgia 2. Pain of dental origin 3. Extracranial 4. Neuropathic 5. Neurovascular 6. Psychogenic
  • 31. Treatment of trigeminal neuralgia is broadly divided into two categories: 1. Destructive treatment:  Radiofrequency Rhizotomies  Balloon Gangliolysis  Stereotactic Radiosurgery (ie Gamma Knife) The possible complication of destructive treatment is facial numbness, neuroparalytic keratitis, or the sever complication of anesthesia dolorosa which is a more complex facial pain.
  • 32. 2. Non destructive treatment:  Medical treatment (Tegretol, Baclofen, Dilantin, etc.)  Microvascular decompression (with initial success rate of 85 to 95%) The possible complication of non destructive treatment is side effect of medication and risk of surgery.
  • 33. Medical management CARBAMAZEPINE 100– 200mg, bd ortid Which provides benefit to more than 75% of patients Common trade names: Tegretol, Tegretol XL, Carbitrol Mode of action Side effects
  • 34. Other Medication  Oxcarbazepine  Gabapentin  Lamotrigine  Baclofen  Topiramate  Sodium valproate  Phenytoin  Clonazepam  Felbamate  Pimozide  Zonisamide  Pregabalin
  • 35. Surgical management Surgical options have been reserved for those patients who have a clearly defined secondary cause for the trigeminal neuralgia, who are unresponsive, who have severe, unremitting pain that limits their ability to eat, for whom multiple medications are intolerable or contraindicated
  • 36. Surgical options Percutaneous glycerol rhizolysis Percutaneous balloon compression Radiofrequency trigeminal (retrogasserian) rhizotomy Gamma knife radiosurgery Microvascular decompression
  • 37.
  • 38. Percutaneous Glycerol Rhizolysis This procedure is used in Arterial or venous compression of the trigeminal nerve Multiple sclerosis Done with absolute alcohol or phenol/glycerol mixture injected phenol or into the trigeminal cistern
  • 39. Hartel technique When the needle pierces the foramen ovale and enters the trigeminal cistern there is usually a characteristic jaw twitch and CSF returns through the needle. Lack of CSF return may be related to poor position of the needle or to scarring within the cistern due to prior surgery
  • 40. Glycerol rhizolysis (GR) Test dose: 0.1-0.15 ml 0.05~0.1 ml at 3~5 min. intervals Total dose: 0.1~0.4 ml Sensory changes: pain, burning or paresthesia
  • 41. Percutaneous balloon compression 0.5 - 1ml of contrast Pear-shape balloon Compression time: 1-7 min.
  • 42.
  • 43. Radiofrequency thermo-coagulation  The theory behind the use of radiofrequency to lesion the trigeminal nerve is that it may selectively injures/destroys the unmyelinated or poorly myelinated nociceptive nerve fibers and spares the (heavily) myelinated fibers which serve touch, proprioception, and motor function
  • 44. Apermanent lesion in the retrogasserian trigemianal nerve is made by beginning at 10Vand approximately 60mAfor a duration of 30-40 sec and increasing to approx. 20Vand 100mA
  • 45.
  • 46. (a) Thermal lesion of trigeminal nerve. (b) Mislocation of the electrode (c) Expansion of thermal energy to neighboring neural structures.
  • 47.
  • 49.  The Gamma focused array intercepting beams Knife is a of 201 of gamma radiation, produced by separate cobalt sources.  The dose is 70–90Gy.  Pain relief is usually not immediate.  The mean time to pain relief in two series was approximately one month.
  • 50. Microvascular decompression It is the only medical or surgical intervention that directly addresses the presumed underlying pathology of classic trigeminal neuralgia. Retrosigmoid craniectomy approach
  • 52.
  • 53.
  • 55. RFL for patients who are elderly or medically frail. Posterior fossa exploration and MVD for younger healthier patients who can tolerate the longer more invasive surgical procedure. GKR as an alternative to RFL in frail or elderly patients. MVD or RFL remains the standard for surgical treatment of younger patients who have considerable life expectancy
  • 57. OMFS…. Peripheral neurectomy Supra orbital Infra orbital Mental Inferior alveolar Long buccal Lingual (rarely)
  • 61. Trigeminal Neuralgia Diet Low fat, high protein, high calorie Easy chewable foods Served lukewarm Offered frequently Trigeminal Neuralgia Association recommends  avoidance of: extreme hot/cold, hot sauce, chili, spicy salsa, mints, black pepper, cinnamon, ginger, nutmeg
  • 62. PUBLIC HEALTH IMPORTANCE  Trigeminal neuralgia has an incidence of 4–5 per 100,000 of the population.  It is nearly twice as common in women,  Incidence increases in age to around 1 in 1000 patients older than 75 years of age.  Rarely,familial cases have been reported.  It is reported that 150,000 people are diagnosed with trigeminal neuralgia every year.
  • 63.  The only indication about the prevalence of TN comes from a study by Penman , who in 1969 reported rates of 107.5/1000000 in men and 200.2/1000000 in women.  TN is therefore a raredisease  TN incidence progressively increases with increasing age: from 17.5/100000/ between 60 and 69 years of age up to 25.6/100000/year after 70.
  • 64.  The female-to-male ratio was 1.74:1 in the Katusic et al. study  and 3:2 in another study by Ashkenazi and Levin.
  • 65. CONCLUSION Population-based epidemiological studies are essential to determine the spectrum of TN symptoms in the population, identifying individuals in whom symptoms are mild enough that they do not seek treatment. Potentially useful approaches in studying the epidemiology of TN include multi-site population-based studies
  • 66. A concerted program of epidemiologic to identify these key studies is needed features of TN: prevalence and public health impact, especially among women and members of minority groups; risk factors; comorbidity; prodromal symptoms; and natural history.
  • 67. REFERENCES: Fonseca, Marciani, Turvey, Oral and Maxillofacial surgery, 2nd edition, volumeII ,Saunders Elsevier, 2009. Jafferey P. Okeson, Bells Orofacial pain, 6th edition, Quintessence publishing co Inc, 2005. Peterson, Ellis, Hupp, Tucker, Oral and maxillofacial surgery, 4th edition, Elsevier, 2003.
  • 68. G.C. Manzoni , P. Torelli, Epidemiology of typical and atypical craniofacial neuralgias, Neurol Sci (2005) 26: S65–S67 Abhishek singh nayyar, Mubeen Khan, Trigeminal Neuralgia: Revisiting clinical characteristics in the Indian scenario. A Journal of Medical science and Technology. Volume I, Issue 2, August 2012; pages 9-17 Cheryl A. Kitt et al., Topical review Trigeminal neuralgia: opportunities for research and treatment, International Association for the Study of Pain, 2000.