Friday, March 28, 2025

CENTRAL NERVOUS SYSTEM EXAMINATION



CENTRAL NERVOUS SYSTEM EXAMINATION 


I. HISTORY TAKING POINTS 

1. Chief Complaints Analysis

When patient reports:

a) Weakness

  • Character: Flaccid, spastic, fatigable, episodic

    • Flaccid → LMN lesion, Peripheral neuropathy, Guillain-Barré syndrome
    • Spastic → UMN lesion (Stroke, MS, Myelopathy)
    • Fatigable → Myasthenia Gravis
    • Episodic → Periodic paralysis, Multiple sclerosis
  • Site:

    • Hemibody → Stroke, Cortical lesion
    • Quadriparesis → High cervical cord lesion, Brainstem
    • Distal weakness → Peripheral neuropathy, Motor neuron disease
    • Proximal weakness → Myopathy, Muscular dystrophy
  • Severity:

    • Rapid progression → Stroke, GBS
    • Slowly progressive → MND, Muscular dystrophy
    • Relapsing-remitting → Multiple sclerosis

b) Sensory disturbances

  • Character: Numbness, tingling, burning, shooting pain

    • Burning → Peripheral neuropathy (diabetes)
    • Shooting → Root compression, Sciatica
    • Loss of vibration/proprioception → Posterior column involvement
  • Site:

    • Glove & stocking → Peripheral neuropathy
    • Dermatomal → Nerve root lesion
    • Hemisensory → Thalamic stroke
    • Sensory level → Spinal cord lesion
  • Severity/Progression:

    • Sudden onset → Infarct
    • Gradual → Tumor, Degeneration

c) Headache

  • Character: Throbbing, dull, lancinating, band-like

    • Throbbing → Migraine
    • Dull, continuous → Tension headache, Tumor
    • Early morning with vomiting → Raised ICP
  • Site:

    • Unilateral → Migraine, Cluster
    • Occipital → Cervical spondylosis, Posterior fossa tumor
  • Severity:

    • Explosive onset → Subarachnoid hemorrhage
    • Progressive → Tumor

d) Seizures

  • Character: Focal, Generalized, Myoclonic, Absence

    • Focal → Structural lesion
    • Generalized → Idiopathic epilepsy, metabolic
    • Myoclonic → Juvenile myoclonic epilepsy
    • Absence → Childhood absence epilepsy
  • Associated features: Aura, post-ictal confusion (Focal onset), tongue bite, incontinence


e) Gait disturbances

  • Type:
    • Hemiplegic gait → UMN lesion
    • Spastic gait → Paraplegia, Cord lesion
    • Ataxic gait → Cerebellar lesion
    • Festinant gait → Parkinsonism
    • High-stepping → Peripheral neuropathy

f) Visual disturbances

  • Character: Blurring, diplopia, field defects, transient vision loss
    • Blurring → Optic neuritis
    • Diplopia → Brainstem lesion, CN palsy
    • Field defects → Optic chiasm lesion (Bitemporal hemianopia)

g) Speech disturbances

  • Aphasia → Cortical (dominant hemisphere)
  • Dysarthria → Brainstem, CN lesion
  • Nasal voice → Palatal paralysis

h) Cognitive or Behavioral changes

  • Acute confusion → Encephalopathy
  • Chronic decline → Dementia, Frontal lobe lesion
  • Personality change → Frontal lobe tumor, Pick's disease

i) Vertigo

  • Peripheral: Severe, positional, with hearing loss (Labyrinthitis)
  • Central: Mild, persistent, with ataxia (Cerebellar stroke)

j) Autonomic dysfunction

  • Orthostatic hypotension → Autonomic neuropathy
  • Bladder dysfunction → Spinal cord involvement

2. Past History

  • Stroke, HTN, DM → Vascular causes
  • Trauma → Epidural/subdural hematoma
  • TB, HIV → Meningitis, Tuberculoma
  • Cancer → Paraneoplastic syndrome, brain metastasis

3. Family History

  • Huntington’s, Parkinson’s, Ataxia → Genetic predisposition
  • Epilepsy → Genetic or structural predisposition

4. Personal History

  • Alcohol → Cerebellar degeneration, Wernicke’s encephalopathy
  • Smoking → Vascular risk, Stroke

5. Occupational/Environmental History

  • Heavy metals → Encephalopathy
  • Rural residence → Neurocysticercosis


II. CLINICAL EXAMINATION POINTS (with diagnostic interpretation)


1. General Examination

  • Neurocutaneous markers:

    • Café-au-lait spots → Neurofibromatosis
    • Ash leaf macules → Tuberous sclerosis
  • Involuntary movements at rest → Parkinsonism, Chorea


2. Higher Mental Function Examination

Consciousness level

  • Drowsy, Comatose → Diffuse brain dysfunction (Trauma, Metabolic, Meningitis)

Orientation

  • Disorientation → Delirium, Dementia

Memory disturbance

  • Immediate → Attention deficit
  • Recent → Hippocampal lesion
  • Remote → Diffuse cortical dysfunction

Language

  • Fluent aphasia → Wernicke’s area lesion
  • Non-fluent → Broca’s area lesion
  • Global aphasia → Large MCA infarct

Apraxia, Agnosia

  • Apraxia → Dominant parietal lesion
  • Agnosia → Occipital/parietal lobe

Frontal lobe dysfunction

  • Disinhibition, impaired judgment

3. Cranial Nerve Examination

II - Optic nerve

  • Visual field defects:
    • Bitemporal hemianopia → Pituitary tumor
    • Homonymous hemianopia → Contralateral occipital/parietal lesion

III, IV, VI

  • Diplopia, ptosis → Brainstem lesion, raised ICP

V

  • Facial numbness → Trigeminal neuralgia, pontine lesion

VII

  • UMN palsy → Forehead sparing
  • LMN palsy → Bell’s palsy

VIII

  • Sensorineural deafness → Acoustic neuroma
  • Nystagmus → Vestibular dysfunction

IX, X

  • Nasal voice, dysphagia → Brainstem lesion

XI

  • Shoulder droop → Accessory nerve lesion

XII

  • Tongue deviation → Ipsilateral LMN lesion, Contralateral UMN lesion

4. Motor System Examination

Bulk

  • Wasting → LMN lesion
  • Hypertrophy → Pseudohypertrophy in Duchenne

Tone

  • Spasticity → UMN lesion
  • Rigidity → Parkinsonism
  • Hypotonia → LMN, Cerebellar lesion

Power

  • Hemiparesis → Stroke
  • Distal weakness → Neuropathy
  • Proximal weakness → Myopathy

Involuntary movements

  • Tremor:
    • Rest → Parkinsonism
    • Intention → Cerebellar
    • Postural → Essential tremor

Reflexes

  • Exaggerated → UMN lesion
  • Absent → LMN lesion
  • Plantar upgoing → Pyramidal tract lesion

Coordination

  • Dysmetria, intention tremor → Cerebellar
  • Dysdiadochokinesia → Cerebellar



Cranial Nerve Examination – Detailed 


I – Olfactory Nerve

Tests:

  • Ask patient to close eyes & occlude one nostril. Present a non-irritant odor (coffee, vanilla, peppermint)
  • Ask to identify the smell. Repeat on both sides.

Interpretation:

  • Anosmia (loss of smell) → Trauma (cribriform plate fracture), Meningioma, Frontal lobe tumor
  • Parosmia (distorted smell) → Temporal lobe epilepsy
  • Hyposmia → Viral infection, aging
  • Hallucinations of smell → Uncinate fits

II – Optic Nerve

Tests:

A. Visual Acuity

  • Snellen’s chart (Distance)
  • Jaeger’s chart (Near vision)

B. Color Vision

  • Ishihara plates

C. Visual Fields

  • Confrontation test
  • Perimetry (Goldmann / Automated Humphrey)

D. Pupillary Reflexes

  • Direct light reflex
  • Consensual light reflex
  • Swinging flashlight test (Relative afferent pupillary defect)

E. Fundoscopy

  • Optic disc, Cup-disc ratio, Pallor, Papilledema, Retinal hemorrhages

F. Red Desaturation Test

  • Tests early optic neuritis

Interpretation:

  • Visual acuity ↓ → Optic neuropathy, Refractive errors
  • Field defects:
    • Bitemporal hemianopia → Pituitary tumor
    • Homonymous hemianopia → Optic tract lesion
    • Central scotoma → Optic neuritis
  • Pupillary reflex abnormal → Optic nerve lesion

III, IV, VI – Oculomotor, Trochlear, Abducens Nerves

These are tested together

Tests:

A. Inspection

  • Ptosis → CN III palsy, Myasthenia

B. Eye Position

  • Strabismus, gaze deviation

C. Extraocular Movements (EOM)

  • Ask patient to follow finger in ‘H’ pattern

D. Diplopia Charting

  • Red-green glasses test
  • Hess chart

E. Convergence Test

F. Nystagmus observation

G. Pupil Size and Reactivity

Interpretation:

  • CN III palsy → Ptosis, ‘Down and out’ eye, Dilated pupil
  • CN IV palsy → Vertical diplopia, Head tilt
  • CN VI palsy → Medial deviation, inability to abduct

V – Trigeminal Nerve

Tests:

A. Sensory (V1, V2, V3 branches)

  • Light touch, pain, temperature over:
    • Ophthalmic
    • Maxillary
    • Mandibular areas

B. Corneal Reflex

  • Afferent: V1
  • Efferent: VII

C. Motor

  • Palpate masseter & temporalis while clenching teeth

D. Jaw jerk reflex

  • Exaggerated in UMN lesion

Interpretation:

  • Loss of sensation in one branch → Peripheral nerve lesion
  • Loss in all divisions → Brainstem lesion, pontine infarct
  • Absent corneal reflex → CN V or VII lesion
  • Weak muscles of mastication → LMN lesion (pons)

VII – Facial Nerve

Tests:

A. Inspection

  • Facial asymmetry, forehead wrinkles, nasolabial fold

B. Motor Tests

  • Ask patient to:
    • Raise eyebrows
    • Close eyes tightly
    • Show teeth
    • Puff cheeks
    • Whistle

C. Taste

  • Anterior 2/3rd of tongue: Sweet, salty

D. Stapedius reflex

  • Hyperacusis if impaired

E. Lacrimation test

Interpretation:

  • LMN lesion → Whole face affected (Bell's palsy)
  • UMN lesion → Forehead spared
  • Loss of taste → Chorda tympani lesion
  • Hyperacusis → Stapedius muscle involvement

VIII – Vestibulocochlear Nerve

Tests:

A. Cochlear Component

  • Finger rub test
  • Rinne’s test: AC > BC (normal)
  • Weber’s test: Lateralization in conductive loss
  • Audiometry (Pure tone)
  • Otoacoustic emissions

B. Vestibular Component

  • Dix-Hallpike maneuver → BPPV
  • Head impulse test → Vestibular hypofunction
  • Romberg’s test
  • Caloric test (COWS – Cold Opposite, Warm Same)

Interpretation:

  • Sensorineural loss → Acoustic neuroma, Labyrinthitis
  • Vertigo with nystagmus → Vestibular neuronitis, Cerebellar stroke

IX & X – Glossopharyngeal & Vagus Nerves

Tests:

A. Palatal Movement

  • Ask patient to say “Ah”
  • Observe uvula deviation

B. Gag Reflex

  • Afferent: IX
  • Efferent: X

C. Phonation

  • Hoarseness, nasal voice

D. Swallowing

E. Cough reflex

Interpretation:

  • Absent gag reflex → IX or X nerve lesion
  • Uvula deviated away from lesion → Unilateral vagus lesion
  • Nasal regurgitation → Palatal palsy

XI – Spinal Accessory Nerve

Tests:

A. Sternocleidomastoid strength

  • Ask patient to turn head against resistance

B. Trapezius strength

  • Shrug shoulders against resistance

Interpretation:

  • Weakness → LMN lesion in posterior triangle (surgical injury) or brainstem lesion

XII – Hypoglossal Nerve

Tests:

A. Tongue Inspection

  • Atrophy, fasciculations

B. Tongue Protrusion

  • Deviation → Towards side of LMN lesion

C. Tongue movement

  • Lateral movement, speed

Interpretation:

  • Deviation towards side of lesion → LMN palsy
  • UMN lesion → Contralateral weakness without atrophy






5. Sensory System Examination

Primary sensations

  • Loss of vibration/proprioception → Posterior column disease
  • Loss of pain/temp → Spinothalamic tract lesion
  • Sensory level → Spinal cord compression

Cortical sensations

  • Astereognosis → Parietal cortex lesion

6. Cerebellar Examination

  • Nystagmus, Dysarthria, Ataxia → Cerebellar lesion
  • Romberg positive → Sensory ataxia

7. Gait Examination

  • Spastic → UMN lesion
  • Ataxic → Cerebellar lesion
  • High stepping → Peripheral neuropathy
  • Parkinsonian → Basal ganglia disease

8. Meningeal Signs

  • Neck stiffness, Kernig’s, Brudzinski’s → Meningitis, SAH

9. Autonomic Nervous System

  • Orthostatic hypotension → Autonomic failure
  • Bladder dysfunction → Spinal cord lesion

10. Psychiatric Evaluation

  • Apathy, Disinhibition → Frontal lobe
  • Delirium → Acute diffuse dysfunction
  • Dementia → Alzheimer’s, Vascular, Lewy body


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