Hypertrophic cranial pachymeningitis and lymphocytic hypophysitis in Sjögren's syndrome
- PMID: 9932974
- DOI: 10.1212/wnl.52.2.420
Hypertrophic cranial pachymeningitis and lymphocytic hypophysitis in Sjögren's syndrome
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.
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