Neurosarcoidosis
Granulomatous multisystem disease of unknown cause, sometimes involving CNS, peripheral nerves, or muscle.
Epidemiology
Prevalence 3–50 per 100,000 population worldwide. More frequent in African Americans than others in United States. Onset age 30–60.
Pathology
Granulomas like those of tuberculosis but without tubercle bacilli or caseation; commonly affect lung, lymph nodes, skin, bone, eyes, salivary glands.
Nervous system involved in 5% of patients: typically basal meninges, causing secondary cranial nerve infiltration and obstructed CSF flow. Granulomas may spread to CNS parenchyma (often hypothalamus). Also peripheral neuropathy, myopathy.

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