Hypertrophic cranial pachymeningitis and lymphocytic hypophysitis in Sjögren's syndrome.

Li, J Y; Lai, P H; Lam, H C; Lu, L Y; Cheng, H H; Lee, J K; Lo, Y K · Neurology · 1999

case_report · Level V

Where this comes from

Abstract

The authors describe a patient with primary Sjögren's syndrome who developed pachymeningitis, hypopituitarism, and central diabetes insipidus. The patient improved with corticosteroid pulse therapy.

Medical subject headings