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Updated: May 12, 2026

Preparation of Mouse Pituitary Immunogen for the Induction of Experimental Autoimmune Hypophysitis
Published on: December 17, 2010
Rapidly evolving hypopituitarism in a boy with multiple autoimmune disorders
Ganesh Jevalikar1, Sze Choong Wong, Margaret Zacharin
1Department of Endocrinology and Diabetes, The Royal Children's Hospital, Murdoch Childrens Research Institute, Melbourne, Victoria, Australia.
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.
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