Rapidly evolving hypopituitarism in a boy with multiple autoimmune disorders. Issue 9 (16th April 2013) - Jevalikar, Ganesh
Abstract: A 10‐year‐old boy with acute onset cranial diabetes insipidus and multiple autoimmune disorders had evolving panhypopituitarism, thought to be due to autoimmune hypophysitis. Over 18 months, a dramatic clinical course with progressive hypopituitarism and development of type 1 diabetes mellitus was evident. Serial brain imaging showed changes suggestive of germinoma.