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Steroid cell tumor of the ovary – A rare case report and review of literature

机译:卵巢类固醇细胞瘤–罕见病例报告并文献复习

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Steroid cell tumors of the ovary are extremely rare, accounting for only 0.1% of all ovarian tumors. Most steroid cell tumors secrete steroid hormones, and only about 10%–15% of patients are asymptomatic. The clinical presentation may take many forms, including abdominal pain, distention, irregular menstrual cycles, and hirsutism. Here, we present a case of a 60-year-old postmenopausal patient who presented with complaints of bleeding per vagina and abdominal pain for 4 months. Ultrasonography (USG) revealed a hypoechoic left adnexal mass measuring 65 mm × 40 mm × 30 mm. Based on these USG findings, the diagnosis of cystic lesion of the left ovary was made. Total abdominal hysterectomy with bilateral salpingo-oophorectomy was done, and the specimen was sent for histopathological analysis. On histopathology, diagnosis of steroid cell tumor-not otherwise specified was offered. This case is reported due to its rarity and its unusual presentation, together with a brief review of the literature of the same.
机译:卵巢类固醇细胞瘤极为罕见,仅占所有卵巢肿瘤的0.1%。大多数类固醇细胞肿瘤分泌类固醇激素,只有约10%–15%的患者无症状。临床表现可能有多种形式,包括腹痛,膨胀,月经周期不规律和多毛症。在这里,我们介绍了一名60岁绝经后患者的病例,该患者每阴道流血和腹部疼痛持​​续4个月。超声检查(USG)显示左回声低,质量为65 mm×40 mm×30 mm。基于这些USG的发现,对左卵巢的囊性病变进行了诊断。进行全腹子宫切除术和双侧输卵管卵巢切除术,并将标本送去进行组织病理学分析。在组织病理学上,提供了没有另外说明的类固醇细胞肿瘤的诊断。据报道此案是由于其稀有性和不寻常的表现,以及对该文献的简要回顾。

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