未特指的卵巢类固醇细胞瘤，伴先天性肾上腺皮质增生症：一种内分泌疾病的罕见肿瘤。
Ovarian steroid cell tumor, not otherwise specified, associated with congenital adrenal hyperplasia: rare tumors of an endocrine disease.
机构信息
Department of Pediatric Surgery, Connecticut Children's Medical Center, Hartford, CT, USA.
出版信息
J Pediatr Surg. 2013 Jun;48(6):E23-7. doi: 10.1016/j.jpedsurg.2013.04.006.
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.
摘要
未特指的卵巢类固醇细胞瘤（OSCTs）非常罕见，在评估卵巢肿块时具有诊断挑战性。我们报告了 1 例此类肿瘤病例，患者患有已知的先天性肾上腺皮质增生症（CAH），继发于 21-羟化酶缺乏症，且不遵医嘱服药。本文描述了这种罕见疾病的检查、诊断和治疗。
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