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作 者:金利娜[1] 田秦杰[1] 郎景和[1] 孙爱军[1] 陈蓉[1] 周远征[1] 周希亚[1] 姜英[2]
机构地区:[1]中国医学科学院北京协和医学院北京协和医院妇产科,北京100032 [2]中国医学科学院北京协和医学院北京协和医院病理科,北京100032
出 处:《生殖医学杂志》2007年第6期400-403,共4页Journal of Reproductive Medicine
摘 要:目的探讨性发育异常患者伴性腺母细胞瘤的临床特征与病因。方法回顾分析了1984年1月至2006年3月间在我院收治的4例性发育异常患者伴性腺母细胞瘤的临床表现、病理特征、治疗及预后。结果4例患者确诊为性腺母细胞瘤时的年龄平均22.5岁;表型均为发育幼稚的女性,无男性化表现,均以原发闭经为主诉;检查发现均含有Y染色体,卵泡刺激素(FSH)[(56.83±12.49)IU/L]和黄体生成素(LH)[(28.25±6.58)IU/L]显著升高,睾酮(T)[(2.85±3.33 nmol/L)]和雌二醇(E2)[(8.91±9.14)pmol/L]水平显著下降,提示性腺功能不良。4例患者全部行双侧性腺切除术。性腺均位于腹腔。性腺母细胞瘤左侧2例,右侧1例,双侧1例。1例随访2月,1例随访20年,无复发,另2例失访。结论性腺母细胞瘤是一种罕见的良性肿瘤,好发于性发育异常患者,治疗宜采取手术切除性腺,术后辅助性激素治疗,预后良好,其病因现尚不清楚。Objective: To investigate the clinical features and etiology of gonadoblastoma in the patients with disorders of sexual development. Methods: Four cases of gonadoblastoma in disorders of sexual development admitted in PUMC Hospital between Jan 1984 and Mar 2006 were summarized and analyzed retrospectively. Results: The mean age of 4 cases at the time of diagnosis was 22.5 years. They all had undeveloped female phenotype without signs of virilism. The chief complaint was primary amenorrhea and they all had Y chromosome in karyotype (3 cases of 46,XY and 1 case of 45,XO/46,XY). FSH (56.83±12.49) IU/L and LH (28. 25±6. 58) IU/L were markedly increased while testosterone (2. 85±3. 33)nmol/L and estrodiol (8.91±9.14)pmol/L were clearly decreased, indicating gonadal dysplasia. They all had bilateral gonadectomy and all gonads were located in abdomen. Gonadoblastoma occurred unilaterally in 3 cases (1 in right gonad, 2 in left gonad) and bilaterally in 1 case. Two patients were followed up for 2 months and 20 years respectively without relapse, and two lost follow-up. Conclusions: Gonadoblastoma is a rare benign tumor often associated with disorders of sexual development, especially in the patients with Y chromosome. These patients should have bilateral gonadectomy and hormone therapy after the operation. The prognosis of gonadoblastoma is good. And the etiology is not yet clear.
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