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Case Reports
. 1999 Jan 15;52(2):420-3.
doi: 10.1212/wnl.52.2.420.

Hypertrophic cranial pachymeningitis and lymphocytic hypophysitis in Sjögren's syndrome

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Case Reports

Hypertrophic cranial pachymeningitis and lymphocytic hypophysitis in Sjögren's syndrome

J Y Li et al. Neurology. .

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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