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Neurology 1999;52:420
© 1999 American Academy of Neurology
Brief Communications

Hypertrophic cranial pachymeningitis and lymphocytic hypophysitis in Sjögren’s syndrome

J.-Y. Li, MD, P.-H. Lai, MD, H.-C. Lam, MD, L.-Y. Lu, MD, H.-H. Cheng, MD, J.-K. Lee, MD and Y.-K. Lo, MD

From the Section of Neurology (Drs. Li and Lo), Department of Radiology (Dr. Lai), Division of Endocrinology, Department of Medicine (Drs. Lam and Lee), and Division of Allergy, Immunology & Rheumatology, Department of Medicine (Drs. Lu and Cheng), Veterans General Hospital, Kaohsiung, Taiwan.

Address correspondence and reprint requests to Dr. J.-Y. Li, Section of Neurology, Veterans General Hospital–Kaohsiung, 386, Ta-Chung 1st Road, Kaohsiung, Taiwan 813, R.O.C.; e-mail: jiehyli{at}ksts.seed.net.tw

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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