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Information

Differential Diagnosis of Nervous System Disorders

= sudden intracranial insult that leaves a permanent neurological residual

Incidence:

Age:>55 years (12% occur in young adults); M÷F = 2÷1

Risk factors: heredity, hypertension (50%), smoking, diabetes (15%), obesity, familial hypercholesterolemia, myocardial infarction, atrial fibrillation, congestive heart failure, alcoholic excess, substance abuse, oral contraceptives, pregnancy, high anxiety + stress

Etiology:

  1. NONVASCULAR (5%): eg, tumor, hypoxia
  2. VASCULAR (95%)
    1. Brain infarction = ischemic stroke (80%)
      1. Occlusive atheromatous disease of extracranial (35%) / intracranial (10%) arteries = large vessel disease between aorta + penetrating arterioles
        • critical stenosis, thrombosis,
        • plaque hemorrhage / ulceration / embolism
      2. Small vessel disease of penetrating arteries (25%) = lacunar infarct
      3. Cardiogenic emboli (6–15–23%)
        • Ischemic heart disease with mural thrombus
          • acute myocardial infarction (3% risk/year)
          • cardiac arrhythmia
        • Valvular heart disease
          • postinflammatory (rheumatic) valvulitis
          • infective endocarditis (20% risk/year)
          • nonbacterial thrombotic endocarditis (30% risk/year)
          • mitral valve prolapse (low risk)
          • mitral stenosis (20% risk/year)
          • prosthetic valves (1–4% risk/year)
        • Nonvalvular atrial fibrillation (6% risk/year)
        • Left atrial myxoma (27–55% risk/year)
      4. Nonatheromatous disease (5%)
        • arterial elongation, coil, kinks (up to 20%)
        • fibromuscular dysplasia (typically spares origin + proximal segment of ICA)
        • aneurysm (rare) may occur in cervical / petrous portion / intracranially
        • dissection: traumatic / spontaneous (2%); up to 15% of strokes in young adults
        • cerebral arteritis (Takayasu, collagen disease, lymphoid granulomatosis, temporal arteritis, Behçet disease, chronic meningitis, syphilis)
        • postendarterectomy thrombosis / embolism / restenosis
      5. Overactive coagulation (5%)
    2. Hemorrhagic stroke (20%)
      1. Primary intracerebral hemorrhage (15%)
        • Hypertensive hemorrhage 45%
        • Amyloid angiopathy 7–17%
        • Anticoagulants 10%
        • Tumor 5–10%
        • Drug use 6%
        • Vascular malformation, aneurysm 5%
        • Bleeding diathesis (eg, hemophilia) <1%
        • Severe migraine
        • Surgery (carotid endarterectomy, heart)
      2. Vasospasm due to nontraumatic SAH (4%)
        • Ruptured aneurysm 75–80%
        • Vascular malformation 10–15%
        • “Nonaneurysmal” SAH 5–15%
      3. Venoocclusive disease (1%): sinus thrombosis

Prognosis:

  1. Death during hospitalization (25%): alteration in consciousness, gaze preference, dense hemiplegia have a 40% mortality rate
    • Hypodensity involving >50% of MCA territory has a fatal outcome in 85%!
  2. Survival with varying degrees of neurologic deficit (75%)
  3. Good functional recovery (40%)

Role of imaging:

  1. Confirm clinical diagnosis
    • Clinical diagnosis is inaccurate in 13%!
  2. Identify primary intracerebral hemorrhage
  3. Detect structural lesions mimicking stroke:
    tumor, vascular malformation, subdural hematoma
  4. Detect early complications of stroke:
    cerebral herniation, hemorrhagic transformation

Indications for cerebrovascular testing:

  1. TIA = transient ischemic attack
  2. Progression of carotid disease to 95–98% stenosis
  3. Cardiogenic cerebral emboli

Temporal classification:

  1. TIA = transient ischemic attack
    • lasts 5 to 30 minutes + clears within 24 hours
  2. RIND = reversible ischemic neurologic deficit
    = fully reversible prolonged ischemic event resulting in minor neurologic dysfunction
    • >24 hours and <8 weeks with eventual total recovery
      Incidence: 16÷100,000 population / year
  3. Progressing stroke / intermittent progressive stroke
    = stepwise / gradually progressing accumulative neurologic deficit evolving over hours / days
  4. Slow stroke
    = rare clinical syndrome presenting as developing neuronal fatigue with weakness in lower / proximal upper extremity after exercise; occurs in patients with occluded ICA
  5. Completed stroke
    = severe + persistent stable neurologic deficit = cerebral infarction (death of neuronal tissue) as end stage of prolonged ischemia >21 days
    • level of consciousness correlates well with size of infarct

    Prognosis: 6–11% recurrent stroke rate