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Hypertrophic cranial pachymeningitis and lymphocytic hypophysitis in Sjögren's syndrome
1Section of Neurology, Veterans General Hospital, Kaohsiung, Taiwan, ROC. jiehyli@ksts.seed.net.tw
Neurology
|February 5, 1999
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.