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  • Title: Rapidly evolving hypopituitarism in a boy with multiple autoimmune disorders.
    Author: Jevalikar G, Wong SC, Zacharin M.
    Journal: J Paediatr Child Health; 2013 Sep; 49(9):783-5. PubMed ID: 23586429.
    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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