Article ID Journal Published Year Pages File Type
4156041 Journal of Pediatric Surgery 2013 5 Pages PDF
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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Health Sciences Medicine and Dentistry Perinatology, Pediatrics and Child Health
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