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Hypertrophic Cranial Pachymeningitis and Lymphocytic Hypophysitis in Sjogren's Syndrome Neurol 52:420-423, Li,J.-Y.,et al, 1999 See this aricle in Pubmed Article Abstract The author describes a patient with primary Sjogren's syndrome who developed pachymeningitis, hypopituitarism, and central diabetes insipidus. The patient improved with corticosteroid pulse therapy.

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(click to filter results - removes previous filter) hypertrophic intracranial pachymeningitis lymphoid adenohypophysitis MRI MRI,abnormal Sjogren's syndrome Sjogren's syndrome,neurologic manifestations of

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