Limaïem F, Lahmar A, Ben Fadhel C, Bouraoui S, M'zabi-Regaya S
Department of Pathology, Mongi Slim Hospital, Sidi Daoued La Marsa (2046), Tunisia.
Pathologica. 2008 Feb;100(1):13-7.
Gynandroblastoma is a rare variant of ovarian sex cord stromal tumours that demonstrates morphological evidence of both male and female differentiation. We report a new case of gynandroblastoma in a 22-year-old nulliparous female with a history of menstrual disturbance. Physical examination disclosed a painless pelvic mass measuring 20 cm across with normal secondary sex characteristics, and no signs of virilisation. Histological examination of the surgically resected primary tumour revealed a predominant adult granulosa cell component admixed with a minor Sertoli cell component that did not exceed 20% of the tumour. Immunohistochemical analysis showed positive immunostaining of Sertoli cell areas with inhibin. The final diagnosis was gynandroblastoma. The post-operative course was uneventful and there was no evidence of recurrence during the 9-month follow-up period.
两性母细胞瘤是卵巢性索间质肿瘤的一种罕见变异型,具有男性和女性分化的形态学证据。我们报告一例22岁未生育女性的两性母细胞瘤新病例,该患者有月经紊乱病史。体格检查发现一个直径20厘米的无痛性盆腔肿块,第二性征正常,无男性化体征。对手术切除的原发肿瘤进行组织学检查,发现主要为成年颗粒细胞成分,混合有少量不超过肿瘤20%的支持细胞成分。免疫组织化学分析显示支持细胞区域抑制素免疫染色呈阳性。最终诊断为两性母细胞瘤。术后过程顺利,在9个月的随访期内无复发迹象。