Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4156041 | Journal of Pediatric Surgery | 2013 | 5 Pages |
Abstract
Ovarian steroid cell tumors, not otherwise specified (OSCTs), are extremely rare and present a diagnostic challenge when evaluating an ovarian mass. We present a case of such a tumor in a patient with known Congenital Adrenal Hyperplasia (CAH), secondary to 21-hydroxylase deficiency, who was noncompliant with her medications. The workup, diagnosis, and treatment of this rare condition are described.
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Authors
Tina T. Thomas, Kimberly R. Ruscher, Srinivas Mandavilli, Fabiola Balarezo, Christine M. Finck,