Bilateral ovary adrenal rest tumor in a congenital adrenal hyperplasia following adrenalectomy.

Objective: In contrast to the high incidence of testicular adrenal rest tumors in adult male patients with congenital adrenal hyperplasia (CAH), ovarian adrenal rest tumors (OARTs) in female CAH patients are rare. In this case report, we describe a case of bilateral OART in a female patient with CAH due to 21-hydroxylase deficiency.

Methods: We present a detailed case report with the clinical, imaging, and laboratory findings of the patient.