Virilising ovarian tumour in a postmenopausal woman after bilateral oophorectomy

A. Coetzee, Jocelynn Ann Hellig, Candice Sher-Lockitz, Annelize Barnard, V. Thomas, M. Conradie
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Abstract

Ovarian neoplasms are rare tumours of steroid cell origin. These tumours present clinically due to the associated excess production of either androgenic or oestrogenic gonadal steroid hormones. The clinical picture is dictated by the specific hormone(s) produced and influenced by the age of the patient. The case is a 59-year-old woman who presented with a five-year history suggestive of androgen excess. She underwent a hysterectomy and right-sided oophorectomy at age 28 years for dysfunctional uterine bleeding. Virilisation was confirmed on clinical examination and the testosterone excess biochemically localised to the ovaries. A left-sided oophorectomy was performed. The clinical picture and testosterone excess persisted after surgery. Follow-up radiological investigations identified adnexal material that on resection proved to be remnant ovarian tissue. Histopathology confirmed the presence of a steroid cell tumour within the remnant tissue. The biochemical androgen excess resolved and the clinical features improved dramatically.
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双侧卵巢切除术后绝经妇女卵巢肿瘤阳刚化
卵巢肿瘤是一种罕见的类固醇细胞肿瘤。这些肿瘤的临床表现是由于相关的雄激素或雌激素性腺类固醇激素的过量产生。临床表现由产生的特定激素决定,并受患者年龄的影响。该病例为59岁女性,5年雄激素过量病史。她在28岁时因功能失调性子宫出血接受了子宫切除术和右侧卵巢切除术。临床检查证实男性化,睾酮过量生化定位于卵巢。行左侧卵巢切除术。手术后临床表现和睾酮过量持续存在。后续放射学检查发现附件物质,经切除证实为卵巢残余组织。组织病理学证实残余组织内存在类固醇细胞瘤。生化雄激素过量得到缓解,临床表现明显改善。
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