362.1 ð é«åžçç
362.1.1 Step 1: Where? (Anatomic Localization)
- Cortex: cognition, language, complex motor/sensory
- Subcortical white matter: connectivity
- Basal ganglia: movement (Parkinson, Huntington)
- Brainstem: cranial nerves, consciousness, long tracts crossing
- Cerebellum: coordination, balance, gait
- Spinal cord: sensory level, UMN below, LMN at
- Nerve root: dermatome/myotome
- Plexus: multiple roots
- Peripheral nerve: length-dependent (longest first)
- NMJ: fatigable, fluctuating
- Muscle: proximal weakness, CK elevated
362.1.2 Step 2: What? (Etiologic Diagnosis)
- Vascular (sudden onset)
- Inflammatory/Infectious (days-weeks)
- Demyelinating
- Neoplastic (progressive)
- Degenerative (slow)
- Traumatic
- Metabolic/Toxic
- Iatrogenic
- Genetic
362.1.3 Key Elements
- Onset (sudden = vascular; gradual = neoplastic, degenerative)
- Duration + course (acute, subacute, chronic; static, progressive, fluctuating, relapsing-remitting)
- Distribution (focal, multifocal, diffuse)
- Associated symptoms (systemic, vascular risks)
- Pre-existing conditions (DM, HTN, autoimmune, cancer)
- Family history
- Medications + substances
- Functional impact
362.1.4 Time Course Clues
| Pattern | Suggests |
|---|---|
| Seconds-minutes | Vascular (stroke), seizure |
| Hours-days | Infection, inflammation |
| Weeks-months | Tumor, autoimmune |
| Months-years | Degenerative, hereditary |
| Fluctuating | NMJ (MG), MS relapses |
| Stepwise | Multi-infarct |
362.1.5 Components
- Mental status: alertness, orientation, attention, memory, language, executive
- Cranial nerves: I-XII
- Motor: strength (0-5 MRC), tone, bulk, fasciculations
- Reflexes: DTRs, plantar (Babinski), primitive
- Sensation: light touch, pinprick, vibration, position, cortical
- Coordination: finger-nose, heel-shin, rapid alternating
- Gait + station: stance, tandem, Romberg
- Special tests: Hoffmann, Lhermitte, etc.
362.1.6 UMN vs LMN
| Feature | UMN | LMN |
|---|---|---|
| Weakness | Yes | Yes |
| Tone | â (spasticity) | â (flaccid) |
| Atrophy | Late | Early, prominent |
| Reflexes | ââ, clonus | â or absent |
| Fasciculations | No | Yes |
| Plantar | Upgoing (Babinski) | Downgoing |
362.1.7 Glasgow Coma Scale (GCS)
- Eye opening (1-4): spontaneous, to voice, to pain, none
- Verbal (1-5): oriented, confused, inappropriate, incomprehensible, none
- Motor (1-6): obeys, localizes, withdraws, flexor, extensor, none
- Total 3-15
362.1.8 CT
- Use: acute hemorrhage, trauma, bone
- Fast, widely available
- Limitations: posterior fossa, subtle lesions, early stroke
362.1.9 MRI
- Definitive for most pathology
- Sequences:
- T1: anatomy, fat bright, fluid dark
- T2: pathology bright (most), fluid bright
- FLAIR: T2 with CSF suppressed; great for MS, edema
- DWI: acute stroke (bright within minutes-hours)
- **T2*/SWI**: hemosiderin, microbleeds
- MRA/MRV: vessels
- Gadolinium: enhancement (BBB disruption, tumor, infection, inflammation)
362.1.10 Other Imaging
- CT/MR angiography: vessels
- DSA (digital subtraction): gold standard for vessels
- PET: FDG (metabolism), amyloid, tau, dopamine transporters
- SPECT: perfusion
362.1.12 EMG + NCS
- Neuropathy: axonal vs demyelinating
- NMJ disorders: decremental response (MG), incremental (LEMS)
- Myopathy: characteristic patterns
362.1.14 Indications
- Meningitis, encephalitis
- SAH (CT-negative)
- MS (oligoclonal bands)
- Inflammatory/autoimmune
- Cancer (LM disease)
- Pressure (IIH, NPH)
362.1.15 Contraindications
- â ICP with mass effect (herniation risk)
- Coagulopathy
- Infection at puncture site
362.1.16 Components
- Opening pressure (normal 10-20 cm H2O)
- Cell count (normal < 5 WBC, no RBCs)
- Protein (normal 15-45 mg/dL)
- Glucose (normal 2/3 of serum)
- Gram stain + culture
- Specific: oligoclonal bands, cytology, flow, autoantibodies, PCR
362.1.17 Patterns
| Condition | Cell count | Protein | Glucose |
|---|---|---|---|
| Bacterial meningitis | ââ PMN | ââ | â |
| Viral meningitis | â lymphs | â mild | Normal |
| TB meningitis | â lymphs | ââ | â |
| Fungal | â lymphs | â | â |
| MS | Mild â lymph | OCB | Normal |
| SAH | Many RBCs | â | Normal |
| GBS | Normal cells | ââ (albuminocytologic) | Normal |
362.1.17.0.1 Genetic Testing
- Hereditary neuropathies
- Muscular dystrophies
- Movement disorders (Huntington, ataxias)
- Mitochondrial diseases
- Familial ALS
- AD genetics (APP, PSEN1, PSEN2, APOE)
362.1.17.1 𩺠åºé鿥
- Localize first, then etiology
- Onset speed â vascular (sudden), inflammatory (days), neoplastic (weeks-months), degenerative (months-years)
- MRI > CT for most neuro pathology; CT for acute bleed
- DWI: acute stroke (bright)
- CSF patterns: bacterial (PMN, â glucose), viral (lymphs, normal glucose), MS (OCB)
- UMN vs LMN distinction critical