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. Author manuscript; available in PMC: 2012 Mar 15.
Published in final edited form as: Expert Opin Pharmacother. 2010 Nov 23;12(1):1–12. doi: 10.1517/14656566.2010.514903

Table 1.

Differential diagnosis of rapidly progressive dementia.

Etiologic Category Examples
Neurodegenerative Prion disease (e.g., Creutzfeldt-Jakob disease)
Alzheimer’s disease
Frontotemporal degeneration
Dementia with Lewy bodies
Corticobasal degeneration
Progressive supranuclear palsy
Oncologic Primary CNS tumor
Metastatic tumor
Autoimmune Hashimoto’s encephalopathy
Paraneoplastic syndrome
Lupus cerebritis
Sjögren’s syndrome
Sarcoidosis
Multiple sclerosis
CNS vasculitis
Isolated angiitis of the central nervous system (IACNS)
Anti-VGKC antibodies
Antineurophil antibodies
Cerebral amyloid inflammatory vasculopathy
Polyarteritis nodosa
Celiac disease
Behçet’s disease
Hypereosinophilic disease
Toxicity Bismuth toxicity
Lithium toxicity
Mercury toxicity
Arsenic toxicity
Alcoholic dementia
Metabolic Vitamin B12 deficiency
Vitamin B1 deficiency (e.g., Wernicke–Korsakoff syndrome)
Niacin deficiency
Folate deficiency
Uremia
Wilson’s disease
Portosystemic encephalopathy
Acquired hepatocerebral degeneration
Porphyria
Electrolyte abnormalities
Infectious Iatrogenic Creutzfeldt–Jakob disease
Variant Creutzfeldt–Jakob disease
AIDS dementia complex
Syphilis
Fungal/viral meningoencephalitis (e.g., aspergillosis, herpes encephalitis)
Whipple’s disease
Progressive multifocal leukoencephalopathy
Subacute sclerosing panencephalitis
Parasitic infections
Lyme disease
Balamuthia
Vascular Stroke
Biswanger’s disease
Hyperviscosity syndromes
CADASIL
Endocrine Hypo-/Hyperthyroidism
Hypo-/Hyperparathyroidism
Adrenal insufficiency
Psychiatric Depression
Psychotic disorders (e.g., schizophrenia)
Conversion disorder
Malingering

CADASIL: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.