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Diabetes insipidus (DI) is an uncommon diagnosis and might be idiopathic or caused by Langerhans cell histiocytosis, brain tumors, congenital anomalies, inflammation, autoimmune conditions, or other disorders. To clarify the natural history of idiopathic DI, researchers reviewed records of two cohorts of pediatric patients diagnosed with DI at multiple referral centers in the U.S.
The first cohort included 105 patients from three centers who were diagnosed with central DI in 1980–1989. Ultimately, 89% of patients had underlying diagnoses identified (including central nervous system tumors, 34%; congenital anomalies, 20%; Langerhans histiocytosis, 19%; and infection, 4%). Eleven percent had idiopathic DI. The second cohort included 30 patient…