CNS

PathologyUpdated 4 min read
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One Liners

  1. While sudden violent, flinging movements of an entire limb = (hemiballismus) = subthalamic nucleus
  2. generalized erratic dance-like jerky movements (chorea) = basal ganglia
  3. Vector of Viral Enchepelitis = House Flies
  4. Autonomic Neuropathy = Postural Hypotension
  5. Most common brain tumor in children = Astrocytoma
  6. Route of tranmission for meningiococcal infections = Bloodstream

Meningitis

Age GroupPrimary Bacterial Etiologies
Neonates (<3 months)1. Group B Streptococcus (S. agalactiae)

2. Escherichia coli

3. Listeria monocytogenes
Children (3 months – 10 years)1. Streptococcus pneumoniae (Most common overall)

2. Neisseria meningitidis
Teens & Young Adults (10 – 19 years)1. Neisseria meningitidis (Highest incidence in teens/dorms)

2. Streptococcus pneumoniae
Adults & Elderly (>20 years)1. Streptococcus pneumoniae

2. Neisseria meningitidis (Adults)

3. Listeria monocytogenes (Elderly/Immunocompromised)

Syndromes

SyndromeCause / LesionKey structures involvedClassic findings / MCQ clues
Costen SyndromeTMJ dysfunctionTemporomandibular jointFacial pain
Ear symptoms
; no true nerve infiltration or palatal paralysis
Sluder SyndromeSphenopalatine ganglion neuralgiaSphenopalatine ganglionSevere facial pain
nasal congestion
lacrimation
Wallenberg Syndrome ⭐PICA infarction → lateral medullaSpinal trigeminal nucleus, spinothalamic tract, nucleus ambiguus, sympathetic fibers, inferior cerebellar peduncleIpsilateral Horner + ipsilateral facial pain/temp loss
contralateral body pain/temp loss
ipsilateral ataxia
dysphagia/hoarseness
Dejerine Syndrome ⭐ASA infarction → medial medullaCN XII, pyramid, medial lemniscusIpsilateral tongue paralysis
contralateral hemiparesis
contralateral loss of vibration/proprioception
Ramsay Hunt Syndrome ⭐⭐⭐VZV reactivation in geniculate ganglionCN VII ± CN VIIIIpsilateral LMN facial paralysis
painful vesicular ear/palatal rash
severe otalgia
; may have vertigo, tinnitus, hearing loss
Trotter Syndrome ⭐⭐⭐Nasopharyngeal carcinoma invading lateral nasopharynx / Sinus of MorgagniEustachian tube + V3 + palatal muscles/innervationIpsilateral conductive hearing loss
ipsilateral facial pain/numbness
ipsilateral palatal paresis
Parkinson Disease ⭐⭐⭐Degeneration of dopaminergic neuronsSubstantia nigra pars compactaResting tremor
rigidity
bradykinesia/akinesia
; Lewy bodies
Frey's Syndrome (Auriculotemporal Syndrome) ⭐⭐⭐Injury/surgery to parotid region, classically after parotidectomyDamaged parasympathetic postganglionic secretomotor fibers

sympathetic fibers supplying sweat glands and cutaneous blood vessels

Gustatory sweating + flushing
over the parotid/cheek region during eating or anticipation of food
Dejerine–Roussy Syndrome (Thalamic Pain Syndrome) ⭐⭐⭐Thalamic stroke/infarctionVPL + VPM nuclei of thalamusSudden contralateral hemisensory loss + sensory ataxiaAs sensation returns → severe, persistent central neuropathic pain, dysesthesia, paresthesia, sensory disturbances, emotional/behavioral changes
Gerstmann Syndrome ⭐⭐⭐,Lesion of the dominant hemisphere (usually left)Angular gyrus, inferior parietal lobuleBrodmann area 39Agraphia + Acalculia + Finger agnosia + Left-right disorientationThe 4 A's → Angular gyrus

Eye

FeatureCN III (Oculomotor)CN IV (Trochlear)CN VI (Abducens)
Innervated Muscle(s)Superior, Inferior, & Medial Recti; Inferior Oblique; Levator Palpebrae Superioris; Pupillary SphincterSuperior ObliqueLateral Rectus
Resting Eye Position"Down and Out" (due to unopposed Lateral Rectus & Superior Oblique)Normal or slightly elevated / extortedMedially deviated (Esotropia / Inward)
Type of DiplopiaHorizontal & vertical diplopiaVertical & torsional diplopia (worse when looking down/reading)Horizontal diplopia (worse when looking toward side of lesion)
Compensatory Head PositionHead turned or tilted to side of lesionHead tilt to the OPPOSITE side (chin tucked)Head turned TOWARD side of lesion
Ptosis (Drooping Lid)Severe ptosis (paralysis of levator palpebrae)AbsentAbsent
Pupil DeficitMydriasis (dilated, fixed pupil) & loss of accommodationNormalNormal
Key Clinical SignInability to adduct, elevate, or depress eye + ptosis + dilated pupilDifficulty walking down stairs or readingInability to abduct the eye (look laterally)

Reflexes

Figure: Reflexes

Ear

Figure: Ear

Basal Ganglia Structures


StructureMain function / roleLesion / DiseaseClassic clinical findingMCQ association
Substantia nigra pars compacta ⭐⭐⭐Produces dopamine → projects to striatum; facilitates movementParkinson diseaseBradykinesia/akinesia + resting tremor + rigidity + mask-like facies↓ Dopamine → Parkinson
Subthalamic nucleus ⭐⭐⭐Part of indirect pathway; increases inhibition of unwanted movementsHemiballismusSudden, violent, flinging movements of contralateral limbsSubthalamic lesion → contralateral hemiballismus
Caudate nucleus ⭐⭐⭐Part of striatum; motor planning + cognitive/procedural functionsHuntington diseaseChorea + behavioral changes + dementiaCaudate degeneration → Huntington
PutamenPart of striatum; regulates motor executionLesions can cause movement disorders; degeneration with caudate in HuntingtonAthetosis / dystoniaPutamen + caudate = striatum
Globus pallidusMajor output nucleus of basal ganglia; GPi inhibits thalamus, GPe regulates subthalamic nucleusLesions associated with dystonia / athetosisSustained muscle contractions, abnormal postures or slow writhing movementsCO poisoning / Wilson disease → basal ganglia injury

Vagus

NerveTarget / FunctionClinical Deficit on Damage
External Laryngeal NerveMotor to cricothyroid muscle (tenses vocal cords to raise pitch)Loss of high-pitched voice; inability to sing high notes
Recurrent Laryngeal NerveMotor to all other intrinsic laryngeal musclesHoarseness, breathy voice; stridor/airway obstruction if bilateral
Internal Laryngeal NerveSensory above the vocal cords (epiglottis, laryngeal vestibule)Loss of cough reflex above vocal cords (risk of aspiration)