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Updated: Jul 25, 2026

Preparation of Mouse Pituitary Immunogen for the Induction of Experimental Autoimmune Hypophysitis
Published on: December 17, 2010
[A case of lymphocytic hypophysitis initially diagnosed as aseptic meningitis]
Eito Miura1, Uran Komatsubara1, Yoshitaka Umeda1
1Department of Neurology, Nagaoka Red Cross Hospital.
None:
A 57-year-old man presented with headache and fever, and was diagnosed as having aseptic meningitis on the basis of CSF pleocytosis. One month later, the symptoms became exacerbated, and lethargy also developed. Although general blood tests including electrolytes and creatine kinase showed no abnormalities, brain MRI with Gd-enhancement revealed enlargement of the whole pituitary gland, spreading to the stalk. Hormonal tests revealed pan-hypopituitarism. After ruling out diseases such as sarcoidosis, syphilis, tuberculosis, Sjögren syndrome and systemic lupus erythematosus, which could potentially cause hypophysitis, lymphocytic hypophysitis was diagnosed. Hormone replacement therapy ameliorated both the symptoms and the enlargement of the pituitary gland. This case was considered to be atypical lymphocytic hypophysitis, lacking abnormalities in general blood tests, which is essential when considering a differential diagnosis of aseptic meningitis.
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