Adult granulosa cell tumor of ovary in a young female: A rare case report

Priyanka Patil, S. Agrawal, N. Dravid, Sumedh S Agrawal, Anand Tambat
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Abstract

Granulosa cell tumours (GCT) belong to the group of sex cord and stromal tumours of ovary. Adult granulosa cell tumours account for approximately 1% of all ovarian tumours and 95% of all granulosa cell tumours. They are found more often in postmenopausal than premenopausal women, with a peak incidence between 50 and 55 years of age. We present the case of a 35-year female who came with white discharge, irregular menses and excessive bleeding during menses since 5 to 6 months. The complete blood picture with peripheral smear examination, kidney and liver function tests were all within normal limits. CT abdomen was advised which revealed a large solid cystic lesion of left ovarian origin. Surgical intervention was done and histopathology revealed adult granulosa cell tumor of ovary.
年轻女性卵巢成人颗粒细胞瘤:罕见病例报告
颗粒细胞瘤(granullosa cell tumors, GCT)属于卵巢性索和间质肿瘤。成人颗粒细胞肿瘤约占所有卵巢肿瘤的1%,占所有颗粒细胞肿瘤的95%。它们在绝经后比绝经前的妇女中更常见,发病率在50至55岁之间达到高峰。我们报告一位35岁的女性,她在月经期间出现白色分泌物,月经不规则和出血过多,自5至6个月以来。全血图、外周涂片检查、肾功能、肝功能检查均正常。腹部CT示左侧卵巢源性大实性囊性病变。经手术治疗,组织病理显示为卵巢成人颗粒细胞瘤。
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