Brainstem and Cranial Nerve Anatomy

Rule of 4. 1

Brainstem Diagrams. 1

Examination – screening. 1

CN I – Olfactory. 1

Eye Examination - Eye Examination. 1

CN II – Optic. 1

CN III – Oculomotor 1

CN IV – Trochlear 1

CN VI – Abducens. 1

CN V – Trigeminal 1

CN VIII – Vestibulocochlear 1

CN IX – Glossopharyngeal 1

CN X – Vagus. 1

CN XI – Accessory. 1

CN XII – Hypoglossal 1

 

Rule of 4

 

4 Rules:

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.


 

Brainstem Diagrams

 


 


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Examination – screening

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

 

CN I – Olfactory

Course

·         Cribriform plate to medial temporal lobe on same side

Examination

·         Loss of smell (anosmia)

·         Test each nostril with familiar smells

Lesions

·         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

Eye Examination - Eye Examination

CN II – Optic

Course

·         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

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CN III – Oculomotor

Anatomy

·         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

Examination

Lesions

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)

CN IV – Trochlear

Anatomy

·         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

Clinical

·         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

Examination

·         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

 

Lesions

·         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

 

CN VI – Abducens

Anatomy

·         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

Examination

·         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.

Lesions

·         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

 

Causes by location

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

 

 

CN V – Trigeminal

 

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

 

CN VIII – Vestibulocochlear

CN IX – Glossopharyngeal

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)

-           

 

 

CN X – Vagus

Nuclei

Course

Function

 

Clinical

 

Examination

 

 

 

CN XI – Accessory

CN XII – Hypoglossal

Examination

-          Inspect tongue for wasting and fasciculations (lower motor neurone lesion)

-          Protrude tongue – deviates towards weaker side

-