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Article in English | IMSEAR | ID: sea-94850

ABSTRACT

Idiopathic granulomatous hypophysitis is a rare entity. The usual clinical presentation is that of an expanding mass lesion with varying degree of hypopituitarism. This patient described presented to us with severe headache along with panhypopituitarism and post-operative diabetes insipidus.


Subject(s)
Adult , Diabetes Insipidus , Diagnosis, Differential , Female , Granuloma/diagnosis , Headache , Humans , Pituitary Diseases/diagnosis , Pituitary Gland/pathology , Pituitary Neoplasms/diagnosis
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