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Adult metastatic yolk sac tumor descending from an intra-abdominal testis: A case report and review of the literature

机译:成人腹腔内睾丸转移性卵黄囊肿瘤1例并文献复习

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摘要

Pure yolk sac tumors are extremely rare in adults; to the best of our knowledge, <20 cases have been reported. Multiple metastases originating from a pure yolk sac testicular tumor, descending from an intra-abdominal testis, are additionally extremely rare. In the present case, a man exhibiting a 30-year history of cryptorchidism and indirect inguinal hernia, was admitted to the Department of Urology (The Second Xiangya Hospital, Changsha, China) due to a mass that had descended from the abdominal cavity 7 months previously. Elevated levels of specific serum marker (-fetoprotein, lactate dehydrogenase and human chorionic gonadotropin) did not indicate potential testicular germ cell types prior to surgery and pathological examination. Pathological results and immunohistochemistry revealed a testicular pure yolk sac tumor subsequent to surgery. The present case report and literature review describes the typical characteristics of an adult testicular yolk sac tumor, as well as the diagnosis and management of the disease.
机译:纯卵黄囊肿瘤在成年人中极为罕见。据我们所知,已经报告了少于20例。另外,来自腹腔内睾丸的纯卵黄囊睾丸肿瘤引起的多发转移极为罕见。在本案中,一名表现出隐睾症和间接腹股沟疝30年历史的男子因肿块从腹腔降落7个月而被收治于泌尿外科(中国长沙湘雅第二医院)。先前。特定血清标志物(甲胎蛋白,乳酸脱氢酶和人绒毛膜促性腺激素)水​​平升高,并不表示手术和病理检查前可能存在睾丸生殖细胞类型。病理结果和免疫组化显示,手术后睾丸为纯卵黄囊肿瘤。本病例报告和文献综述描述了成人睾丸卵黄囊肿瘤的典型特征以及该疾病的诊断和治疗。

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