Brainstem and Cranial Nerve Anatomy
Eye
Examination - Eye Examination
1. There are 4 structures in the midline beginning with M
a. Motor pathway (contralateral corticospinal weakness)
b. Medial lemniscus (contralateral dorsal column sensory loss)
c. Medial Longitudinal fasciculus (ipsilateral INO)
d. Motor nuclei
2. There are 4 lateral structures beginning with S
a. Spinocerebellar pathways (ipsilateral ataxia)
b. Spinothalamic (contralateral pain and temperature loss)
c. Sensory nucleus of the 5th CN
d. Sympathetic pathway (ipsilateral horner’s syndrome)
3. There are 4 cranial nerves in the medulla, 4 in the pons, and 4 above the pons
4. The 4 midline motor nuclei divide into 12 (3, 4, 6, 12) the others (5, 7, 9, 11) are in the lateral brainstem.





CNI
·
Best to just ask if patient has problem with smell
CNII
·
Acuity
CNIII, IV, VI
·
Eye movements
CNV
·
Sensation in three divisions
o
Efferent CN V
o
Afferent CN VII
o
Masseter contraction
o
Jaw opening
o
+/- Jaw jerk
CNVII
·
Facial strength
CNVIII
·
Hearing
CN IX, X
·
Palate symmetry
CN XI
·
Head rotation
CN XII
·
Tongue protrusion
Multiple Cranial Neuropathies
Malignant
Carcinomatous or lymphomatous meningitis
Metastases
Local tumour invasion – nasopharyngeal tumour, sarcoma, cordoma
Perineural invasion – SCC, BCC
Infections
Radiculitis/meningeal infections - TB, fungal, syphilis, lyme
Direct neural infection – Listeria, HIV, CMV, Herpes zoster
Botulism
Inflammatory
Sarcoid
Wegener granulomatosis
Sjogren syndrome
Mixed connective tissue disease
(Myasthenia gravis)
Idiopathic
Tolosa-Hunt like syndrome
Melkersson-Rosenthal syndrome
Idiopathic pachymeningitis
Post-infectious – GBS type
Vascular
Carotid dissection or Jugular occlusion at the skull base
Other
Trauma
Paget disease of skull base
Arnold Chiari malformation
·
Cribriform plate to medial temporal lobe on same
side
·
Loss of smell
·
Test each nostril with familiar smells
·
Causes of anosmia – most are bilateral
·
URTI
·
Smoking
·
Age
·
Ethmoid tumours
·
Basal skull fractures or frontal fracture
·
Post-pituitary surgery
·
Congenital
·
Frontal lobe base disease
o
Meningioma of the olfactory groove
o
Post basal meningitis
o
Sarcoidosis
·
Retina – optic nerve – optic chiasm
·
Optic tract – lateral geniculate body
·
Optic radiation – visual cortex
·
Light reflex fibres – branch off optic tract to
superior colliculus (and synapse with fibres of third nerve)
Examination
·
Acuity
·
Fields
o
Hat pin
o
Glasses off
o
Fields then map scotoma
·
Fundoscopy

·
Nuclei -
peri-aqueductal grey matter in mid-brain at
level of superior colliculus
·
Nerve exits anterior midbrain near cerebral
peduncle
·
Travels between superior cerebrallar
artery and PCA
·
Travel along PCOM and lateral to ICA
·
Through cavernous sinus and superior orbital
fissure.
·
Visceral (Edinger-Westphal nucleus)
o
Lies dorsal to somatic nucleus
o
Supplies cilliary
dilation and cilliary muscles (accommodation)
Pupils
-
Third nerve supplies parasympathetic fibres to the
pupil via Edinger-Wetphal nucleus – cilliary dilation and papillary accommodation.
-
Sympathetic supply comes via ascending sympathetic
fibres from the spinal cord (C8-T2)
Eye movements
-
Supplies all muscles except lateral rectus and
superior oblique
Other
-
Levator palpebrae –
elevates eyelid
Third nerve lesions
·
Ipsilateral weakness of :
1.
Adduction (Medial rectus)
2.
Elevation
3.
Depression
·
Dilated pupil – unreactive to light (direct or
consensual) or accommodation
Causes
·
Central
o
Vascular, tumour demyelination
·
Peripheral
o
Compressive lesions
o
Tumour
o
Basal meningitis
o
Nasopharyngeal or orbital tumours
o
Ischaemia
o
DM
o
Cavernous sinus disease (see above – painful opthalmoplegia)
·
Nucleus, caudal to CNIII nucleus –
periaqueductal grey matter at level of inferior colliculus in midbrain.
·
The only cranial nerve to emerge dorsally from
the brainstem
·
Crossed over after emerging
·
Travels ventrally and thus has longest course
of all cranial nerves (75mm)
·
Passes b/n superior cerebellar artery and PCA
·
Travels through cavernous sinus
·
Supplies superior oblique – intorts the eye,
also depression and abducts
·
Diplopia is common, especially when looking down
(going down stairs and reading)
o
Vertical or oblique diplopia
·
May walk with head tilted to side opposite
lesion to maintain binocular vision
·
May be head tilt away from side of lesion
·
Elevation (hypertropia)
of the affected eye
o
Worse when looking away from the affected side
·
Unable to move eye in and down
·
Examination findings are greater with head
tilted to side of lesion.
·
In patients with CNII lesion it may be hard to
tell if IV is intact
o
Ask patient to abduct eye affected with CNII
palsy and then watch for subtle intorsion as they try
to look down
·
Most common causes
o
Trauma
o
Decompensation of congenital CN IV lesion
o
Microvascular ischaemia
·
Other causes by location
|
Location of lesion |
Associated
Sx |
Causes |
|
Nucleus
(midbrain) |
Contralateral Sup Oblique weakness and
Ipsilateral Horners |
Trauma Infarction Neoplasm |
|
Fascicle
|
Rare Contralateral ataxia |
Superior cerebellar peduncle
pathology |
|
Subarachnoid
space |
Isolated |
Trauma Microvascular Meningitis Tumour |
|
Cavernous
sinus |
See Cavernous sinus syndrome |
|
|
Orbital
apex |
See orbital apex syndromes |
|
·
Nucleus – in the centre of the pons, beneath the
floor of the 4th ventricle, adjacent to CNVII
·
Exits brainstem anteriorly at ponto-medullary junction
·
Runs up the front of the brainstem
·
Past basilar artery, over crest of petrous part
of temporal bone (point of compression in raised ICP)
·
Through cavernous sinus, superior orbital
fissure
·
Supplies lateral rectus
·
Inward deviation of eye (esotropia)
·
Can sometimes appear comitant
·
One and a half syndrome
o
CN VI and ipsilateral MLF lesion
o
Either eye unable to look to side of lesion,
only contralateral eye able to look away from lesion.
·
Common and specific causes
o
Raised ICP
o
Low ICP – especially with spinal CSF leak which
may cause downward pressure.
o
Microvascular
o
Congenital (Duane or Mobius Syndrome)
·
Bilateral disease
o
Raised ICP
o
Meningitis
·
Mimics
o
Thalamic esotropia
o
Convergence spasm
|
Site |
Associated Sx |
Causes |
|
Nucleus (pons) |
Conjugate gaze
palsy (One and a half syndrome) Ipsilateral CNVII |
Stroke Neoplasm |
|
Fascicle (pons) |
Contralateral
hemiparesis +/- other signs |
Stroke Neoplasm Demyelination |
|
Subarachnoid
space |
Isolated |
Microvascular Raised ICP (or
low ICP) Meningitis Trauma Tumour Petrous apex
infection Vertebral/Basilar
dilation/aneurysm Chiari
malformation |
|
Cavernous sinus |
See cavernous
sinus syndrome |
|
|
Orbital Apex |
See Orbital apex
syndromes |
|
Examination
-
Sensation
-
Corneal reflex
-
Masseter contraction
-
Jaw opening – deviates to side of lesion
CNVII
Functions
-
Muscles
-
Taste on the anterior two-thirds of the tongue
-
Lacrimal and salivary glands
Examination
-
Muscle function
-
Taste on tongue
-
Lacrimation (schirmers
test)
Lesions
Nuclei
-
Medulla
Course
-
Formed by rootlets from groove between olive and
inferior cerebellar peduncle
-
Travels closely with vagus
and exits at jugular foramen
Function
-
Taste from the posterior third of the tongue
-
Motor and sensory to pharynx and larynx with vagus
-
Stylopharyngeus is the only skeletal
muscle innervated
-
Carotid baroreceptors
Clinical
-
Dysphagia, choking
-
Often with hoarseness due to vagus
nerve damage
Lesions
-
Medulla infarction
-
Tumour near jugular foramen – will affect vagus as well
-
Internal carotid aneurysm or jugular bulb thrombosis
-
Vincristine toxicity – jaw pain
Examination
-
Elevation of pharynx (vagus
and glossopharyngeal)
-
Decreased saliva production (never actually tested)
-
Test for bilateral sensation to the pharynx and
posterior tongue, this may also elicit a gag reflex
-
Asymmetry of gag reflex is most indicative of
pathology (sensory component of reflex is glossopharyngeal,
motor is vagus)
-
Nuclei
Course
Function
Clinical
Examination
Examination
-
Inspect tongue for wasting and fasciculations
(lower motor neurone lesion)
-
Protrude tongue – deviates towards weaker side
-