TROCHLEAR NERVE
BY- DR. PRIYANKA RAJ
• 4TH cranial nerve
• Motor in function, supplies only
superior oblique
• Only cranial nerve that arises from
the dorsal aspect of the brain
• Only cranial nerve to cross
completely to the other side (arises
from the contralateral nucleus)
• Longest and thinnest of all cranial
nerves
FUNCTIONAL COMPONENTS
• SOMATIC EFFERENT- movement of the eyeball through superior
oblique muscle
• GENERAL SOMATIC AFFERENT- proprioceptive impulses from superior
oblique relayed in mesencephalic nucleus of trigeminal nerve
NUCLEUS
• Midbrain- Ventromedial part of
central gray matter at the level
of inferior colliculus
• Caudal to and continuous with
3rd nerve nucleus complex
• Belongs to somatic efferent
column of nuclei and closely
related to medial longitudinal
bundle
CONNECTIONS OF THE NUCLEUS
• CEREBRAL CORTEX-
• Motor cortex (precentral gyrus) corticonuclear tracts
• Visual cortex superior colliculus & tactobulbar tract
• Frontal eye fields
• Nuclei of 3rd, 6th & 8th cranial nerves  medial longitudinal bundle
• Superior colliculi  descenginf predorsal bundle
• Vertical & torsional gaze centres
• Cerebellum vestibular nuclei
COURSE AND DISTRIBUTION
• PARTS
1. Fascicular part
2. Precavernous part
3. Intracavernous part
4. Intraorbital part
FASCICULAR PART
• Nucles efferent fibres
posteriorly around the
aqueductal gray matter
anterior medullary velum
decussate completely
PRECAVERNOUS PART
• Superior medullary vellum frenulum
veli (below inf. colliculus) dorsal
aspect of midbrainjust above
pons winds around cerebral
peduncle b/w posterior cerebral &
superior cerebellar arteries lateral
to cerebral peduncle posterior
corner of roof of cavernous sinus
INTRACAVERNOUS PART
• Cavernous sinus lateral wall
below oculomotor + above 1st
div of trigeminal ant part
crosses over 3rd nerve lateral
part of superior orbital fissure
INTRAORBITAL PART
• Superior orbital fissure above
the origin of LPS orbital
surface of superior oblique
• Extra fibres in intraorbital part
carry proprioceptive impulses
join ophthalmic division of 5th
nerve in cavernouos
sinusrelay in mesencephalic
nucleus of 5th nerve
SUPERIOR OBLIQUE MUSCLE
• PRIMARY POSITION OF GAZE
• Primary action- INTORSION (along A-P axis)
• Secondary action- DEPRESSION (along horizontal
axis)
• Tertiary action- ABDUCTION ( along vertical axis)
• GLOBE 51° ADDUCTED
• Axis of muscle rotation coincides with optical axis
• DEPRESSION only
• GLOBE 39° ABDUCTED
• Optical axis and line of pull of muscle mae an angle
of 90°
• INTORSION only
4th NERVE PARALYSIS
1. CONGENITAL- 40%
2. TRAUMA- 34%
• Usually bilateral
• Impact on anterior medullary velum at decussation
3. IDIOPATHIC- 20%
4. VASCULAR AND NEUROGENIC- 3-5%
• in older individuals microvasculopathy secondary to diabetes
atherosclerosis or hypertension
• Aneyrusms and tumor
• Ocular myasthenia- isolated unilateral
• SO palsy is most common form of paralytic squint
CLINICAL FEATURES
• The features of nuclear , fasicular and
peripheral 4th nerve palsies are
clinically identical
• nuclear lesions produce
CONTRALATERAL superior oblique
weakness.
SYMPTOMS :
DIPLOPIA : Acute onset of a vertical
diplopia, which is more on downward
gaze ,it is noted by patients while
coming down stairs and while doing
near work.
SIGNS :
1)HYPERTROPIA – the involved eye is
higher as a result of weakness of the
superior oblique muscle, which
becomes more prominent when the
head is tilted towards the ipsilateral
shoulder
2)RESTRICTED OCULAR MOVEMENTS:
there is limitation of depression on
adduction.
3)ABNORMAL HEAD POSTURE:
to avoid diplopia ,head takes a
posture towards the action of the
superior oblique muscle, face is
slightly turned to the opposite side,
chin is depressed, and head is tilted
towards the opposite side.
HEAD IS TILTED TO THE RIGHT.
FACE IS TURNED TO THE RIGHT.
CHIN IS DEPRESSED
UNILATERAL PALSY BILATERAL PALSY
EXOTROPIA IN
DOWNWARD GAZE
little V-pattern exotrpia
TORSION (double
Maddox rod test)
Excyclodeviation <10° Excyclodeviation > 10°
DUCTIONS Normal or diminished diminished
HEAD TILT TEST Positive for involved eye
Hypertropia increases on
tilting head towards
ipsilateral shoulder
Tilting to either side
increases hypertropia
PARK-BIELSCHOWSKY TEST:
• STEP 1 :( to assess which eye is
hypertropic in the primary gaze.)
• In case of left hypertropia, the
following four muscles could be
involved:
• 1) Depressors of the left eye i.e SO
or IR
• 2) Elevators of the right eye i.e the
SR or IO.
• In a 4th nerve palsy the involved
eye is always higher.
• STEP 2 : (which lateral direction has
worse hypertropia )
• If the left hypertropia increases on
right gaze implicates a left superior
oblique or right superior rectus
involvement.
• Increase in the left gaze implicates that
either the right inferior oblique or left
inferior rectus are involved.
• In 4th nerve palsy the deviation IS
WORSE ON OPPOSITE GAZE . (WOOG)
• After step one and step two in Park’s three step test, one is always left
with two muscles
• Either two superior muscles or
• Two inferior muscles
• E.g.,
• RSO or LSR
• LSO or RSR
• LIO or RIR
• RIO or LIR
• STEP 3: ( in which head tilt direction is the hypertropia worse )
• BIELSCHOWSKY HEAD TILT TEST
• The head tilt test is performed with the patient fixating at a straight
ahead target at 3 mts.
• If a superior muscle is weak, HT greater on tilt toward involved muscle
• If an inferior muscle is weak, HT greater on head tilt opposite involved
side
• Increase in left hypertropia on left head tilt implies the left superior
oblique is involved , and increase in right hypertropia on left head tilt
indicates the right inferior rectus is involved.
• In 4th nerve palsy the deviation is BETTER ON OPPOSITE TILT(BOOT).
Hypertropia
Gaze
Gaze where
HT is larger
Head tilt where
HT is larger
RSO palsy R L R
LSO palsy L R L
In Right SO palsy , on right head tilt RSR
will work thus the eye will move upwards
• 4TH CONFIRMATORY STEP: (is the hypertropia worse in upgaze or
downgaze)
• If the left hypertropia increases on down gaze it confirms that the left
superior oblique is involved .
• Helps to rule out mimickers like myasthenia and thyroid disease.
DOUBLE MADDOX ROD TEST
For measuring the degree of
cyclodeviation.
In unilateral palsy – cyclodeviation <10 deg
In bilateral palsy – cyclodeviation >10 deg
SYNDROMES
1. Nuclear- fasicular
2. Subarachnoid space syndrome
3. Cavernous sinus syndrome
4. Orbital syndrome
5. Isolated 4th nerve palsy
1. -NUCLEAR- FASICULAR
• Difficult to distinguish nuclear and fasicular lesions due to short
course of fascicles within midbrain
1. Haemorrhage
2. Infarction
3. Demyelination
4. Trauma
• Fascicular lesions may get contralateral Horner’s syndrome; and
trauma (especially near anterior medullary velum) may cause bilateral
CN IV palsies
• 2. SUBARACHNOID SPACE-
• Closed hea trauma
• Meningitis
• Neoplasms like- pinealomas, tentorial meningiomas
• aneurysms
• 3. CAVERNOUS SINUS SYNDROME
• Associated with 3rd, 5th, 6th nerve palsies and ocular sympathetic
paralysis
3. ORBITAL SYNDROME
• Trauma
• Infalmmation
• Tumors
• Seen in association with other cranial nerve palsies: 3rd, 5th, 6th
• Associated with
• Proptosis
• Chemosis
• Conjunctival congestion
ISOLATED SUPERIOR OBLIQUE PALSY
• Most common etiologies are congenital and traumatic
1. CONGENITAL-
• large vertical fusion amplitude (10-15 prism diopters)
• FAT- family album tomography scan
2. ACQUIRED-
• In ischaemic conditions- diabetes, herpes zoster
Differential Diagnosis of Vertical Binocular Diplopia
• Superior Oblique Palsy
• Thyroid Ophthalmopathy
• Myasthenia Gravis
• Brown Syndrome
• Orbital fracture with entrapment
• Cyclovertical paresis or overaction
• Skew Deviation/Ocular Tilt
• Dissociated Vertical Deviation
MANAGEMENT
• NONSURGICAL- prisms
• CONGENITAL:large hypertropia in PP treated by SO tucking
• ACQUIRED:
SMALL- ipsilateral IO weakening.
MODERATE- ipsilateral IO weakening with ipsilateral SR weakening .
PURE EXCYCLOTROPIA: without hypertropia –HARADA- Ito procedure
Splitting & ALT OF lateral half of SO tendon.
THANK YOU

Trochlear nerve

  • 1.
  • 2.
    • 4TH cranialnerve • Motor in function, supplies only superior oblique • Only cranial nerve that arises from the dorsal aspect of the brain • Only cranial nerve to cross completely to the other side (arises from the contralateral nucleus) • Longest and thinnest of all cranial nerves
  • 3.
    FUNCTIONAL COMPONENTS • SOMATICEFFERENT- movement of the eyeball through superior oblique muscle • GENERAL SOMATIC AFFERENT- proprioceptive impulses from superior oblique relayed in mesencephalic nucleus of trigeminal nerve
  • 4.
    NUCLEUS • Midbrain- Ventromedialpart of central gray matter at the level of inferior colliculus • Caudal to and continuous with 3rd nerve nucleus complex • Belongs to somatic efferent column of nuclei and closely related to medial longitudinal bundle
  • 6.
    CONNECTIONS OF THENUCLEUS • CEREBRAL CORTEX- • Motor cortex (precentral gyrus) corticonuclear tracts • Visual cortex superior colliculus & tactobulbar tract • Frontal eye fields • Nuclei of 3rd, 6th & 8th cranial nerves  medial longitudinal bundle • Superior colliculi  descenginf predorsal bundle • Vertical & torsional gaze centres • Cerebellum vestibular nuclei
  • 7.
    COURSE AND DISTRIBUTION •PARTS 1. Fascicular part 2. Precavernous part 3. Intracavernous part 4. Intraorbital part
  • 8.
    FASCICULAR PART • Nuclesefferent fibres posteriorly around the aqueductal gray matter anterior medullary velum decussate completely
  • 9.
    PRECAVERNOUS PART • Superiormedullary vellum frenulum veli (below inf. colliculus) dorsal aspect of midbrainjust above pons winds around cerebral peduncle b/w posterior cerebral & superior cerebellar arteries lateral to cerebral peduncle posterior corner of roof of cavernous sinus
  • 11.
    INTRACAVERNOUS PART • Cavernoussinus lateral wall below oculomotor + above 1st div of trigeminal ant part crosses over 3rd nerve lateral part of superior orbital fissure
  • 13.
    INTRAORBITAL PART • Superiororbital fissure above the origin of LPS orbital surface of superior oblique • Extra fibres in intraorbital part carry proprioceptive impulses join ophthalmic division of 5th nerve in cavernouos sinusrelay in mesencephalic nucleus of 5th nerve
  • 15.
    SUPERIOR OBLIQUE MUSCLE •PRIMARY POSITION OF GAZE • Primary action- INTORSION (along A-P axis) • Secondary action- DEPRESSION (along horizontal axis) • Tertiary action- ABDUCTION ( along vertical axis) • GLOBE 51° ADDUCTED • Axis of muscle rotation coincides with optical axis • DEPRESSION only • GLOBE 39° ABDUCTED • Optical axis and line of pull of muscle mae an angle of 90° • INTORSION only
  • 16.
    4th NERVE PARALYSIS 1.CONGENITAL- 40% 2. TRAUMA- 34% • Usually bilateral • Impact on anterior medullary velum at decussation 3. IDIOPATHIC- 20% 4. VASCULAR AND NEUROGENIC- 3-5% • in older individuals microvasculopathy secondary to diabetes atherosclerosis or hypertension • Aneyrusms and tumor • Ocular myasthenia- isolated unilateral • SO palsy is most common form of paralytic squint
  • 17.
    CLINICAL FEATURES • Thefeatures of nuclear , fasicular and peripheral 4th nerve palsies are clinically identical • nuclear lesions produce CONTRALATERAL superior oblique weakness. SYMPTOMS : DIPLOPIA : Acute onset of a vertical diplopia, which is more on downward gaze ,it is noted by patients while coming down stairs and while doing near work.
  • 18.
    SIGNS : 1)HYPERTROPIA –the involved eye is higher as a result of weakness of the superior oblique muscle, which becomes more prominent when the head is tilted towards the ipsilateral shoulder 2)RESTRICTED OCULAR MOVEMENTS: there is limitation of depression on adduction.
  • 19.
    3)ABNORMAL HEAD POSTURE: toavoid diplopia ,head takes a posture towards the action of the superior oblique muscle, face is slightly turned to the opposite side, chin is depressed, and head is tilted towards the opposite side. HEAD IS TILTED TO THE RIGHT. FACE IS TURNED TO THE RIGHT. CHIN IS DEPRESSED
  • 20.
    UNILATERAL PALSY BILATERALPALSY EXOTROPIA IN DOWNWARD GAZE little V-pattern exotrpia TORSION (double Maddox rod test) Excyclodeviation <10° Excyclodeviation > 10° DUCTIONS Normal or diminished diminished HEAD TILT TEST Positive for involved eye Hypertropia increases on tilting head towards ipsilateral shoulder Tilting to either side increases hypertropia
  • 21.
    PARK-BIELSCHOWSKY TEST: • STEP1 :( to assess which eye is hypertropic in the primary gaze.) • In case of left hypertropia, the following four muscles could be involved: • 1) Depressors of the left eye i.e SO or IR • 2) Elevators of the right eye i.e the SR or IO. • In a 4th nerve palsy the involved eye is always higher.
  • 22.
    • STEP 2: (which lateral direction has worse hypertropia ) • If the left hypertropia increases on right gaze implicates a left superior oblique or right superior rectus involvement. • Increase in the left gaze implicates that either the right inferior oblique or left inferior rectus are involved. • In 4th nerve palsy the deviation IS WORSE ON OPPOSITE GAZE . (WOOG)
  • 23.
    • After stepone and step two in Park’s three step test, one is always left with two muscles • Either two superior muscles or • Two inferior muscles • E.g., • RSO or LSR • LSO or RSR • LIO or RIR • RIO or LIR
  • 24.
    • STEP 3:( in which head tilt direction is the hypertropia worse ) • BIELSCHOWSKY HEAD TILT TEST • The head tilt test is performed with the patient fixating at a straight ahead target at 3 mts. • If a superior muscle is weak, HT greater on tilt toward involved muscle • If an inferior muscle is weak, HT greater on head tilt opposite involved side
  • 25.
    • Increase inleft hypertropia on left head tilt implies the left superior oblique is involved , and increase in right hypertropia on left head tilt indicates the right inferior rectus is involved. • In 4th nerve palsy the deviation is BETTER ON OPPOSITE TILT(BOOT). Hypertropia Gaze Gaze where HT is larger Head tilt where HT is larger RSO palsy R L R LSO palsy L R L
  • 26.
    In Right SOpalsy , on right head tilt RSR will work thus the eye will move upwards
  • 28.
    • 4TH CONFIRMATORYSTEP: (is the hypertropia worse in upgaze or downgaze) • If the left hypertropia increases on down gaze it confirms that the left superior oblique is involved . • Helps to rule out mimickers like myasthenia and thyroid disease.
  • 29.
    DOUBLE MADDOX RODTEST For measuring the degree of cyclodeviation. In unilateral palsy – cyclodeviation <10 deg In bilateral palsy – cyclodeviation >10 deg
  • 31.
    SYNDROMES 1. Nuclear- fasicular 2.Subarachnoid space syndrome 3. Cavernous sinus syndrome 4. Orbital syndrome 5. Isolated 4th nerve palsy
  • 32.
    1. -NUCLEAR- FASICULAR •Difficult to distinguish nuclear and fasicular lesions due to short course of fascicles within midbrain 1. Haemorrhage 2. Infarction 3. Demyelination 4. Trauma • Fascicular lesions may get contralateral Horner’s syndrome; and trauma (especially near anterior medullary velum) may cause bilateral CN IV palsies
  • 33.
    • 2. SUBARACHNOIDSPACE- • Closed hea trauma • Meningitis • Neoplasms like- pinealomas, tentorial meningiomas • aneurysms
  • 34.
    • 3. CAVERNOUSSINUS SYNDROME • Associated with 3rd, 5th, 6th nerve palsies and ocular sympathetic paralysis
  • 35.
    3. ORBITAL SYNDROME •Trauma • Infalmmation • Tumors • Seen in association with other cranial nerve palsies: 3rd, 5th, 6th • Associated with • Proptosis • Chemosis • Conjunctival congestion
  • 36.
    ISOLATED SUPERIOR OBLIQUEPALSY • Most common etiologies are congenital and traumatic 1. CONGENITAL- • large vertical fusion amplitude (10-15 prism diopters) • FAT- family album tomography scan 2. ACQUIRED- • In ischaemic conditions- diabetes, herpes zoster
  • 37.
    Differential Diagnosis ofVertical Binocular Diplopia • Superior Oblique Palsy • Thyroid Ophthalmopathy • Myasthenia Gravis • Brown Syndrome • Orbital fracture with entrapment • Cyclovertical paresis or overaction • Skew Deviation/Ocular Tilt • Dissociated Vertical Deviation
  • 38.
    MANAGEMENT • NONSURGICAL- prisms •CONGENITAL:large hypertropia in PP treated by SO tucking • ACQUIRED: SMALL- ipsilateral IO weakening. MODERATE- ipsilateral IO weakening with ipsilateral SR weakening . PURE EXCYCLOTROPIA: without hypertropia –HARADA- Ito procedure Splitting & ALT OF lateral half of SO tendon.
  • 39.