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. 1995 May-Jun;1(3):161-2.
doi: 10.4158/EP.1.3.161.

Meningioma in congenital adrenal hyperplasia

P S Strumph  1 , M T Stechison, P A Lee
Affiliations

Meningioma in congenital adrenal hyperplasia

P S Strumph et al. Endocr Pract. 1995 May-Jun.

Abstract

A diversity of malignancies have been reported in patients with congenital adrenal hyperplasia. We report a case of multiple meningiomas, tumors which are more common in females and reported to have sex steroid receptors, in a 46,XX male (severe female hermaphrodite raised as a male) with 21-hydroxylase deficiency. The patient has been treated with glucocorticoids since 3 years of age and testosterone since puberty.

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