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2例儿童家族性睾丸畸胎瘤:家族报告及文献复习

Familial testicular teratoma in 2 children: familial report and review of the literature.

作者信息

Shinohara M, Komatsu H, Kawamura T, Yokoyama M

出版信息

J Urol. 1980 Apr;123(4):552-5. doi: 10.1016/s0022-5347(17)56017-6.

Abstract

Familial occurrence of a testicular tumor is rare. We report mature teratomas in 2 first cousins in a consanguineous family. The cases were unique because both tumors were pathologically similar and their onsets were close. Of 34 families with testicular neoplasms reviewed this is the first family composed of 2 affected children with mature teratomas. The analysis of the familial cases showed segregation of twins and a slightly higher incidence of bilateral tumors. The genetic roles are discussed in the etiology of testicular tumor.

摘要

睾丸肿瘤的家族性发病很罕见。我们报告了一个近亲家族中2名第一代堂兄弟患有成熟畸胎瘤的病例。这些病例很独特,因为两个肿瘤在病理上相似且发病时间相近。在回顾的34个患有睾丸肿瘤的家族中,这是第一个由2名受影响儿童患有成熟畸胎瘤组成的家族。对家族性病例的分析显示了双胞胎的分离现象以及双侧肿瘤的发生率略高。文中讨论了遗传因素在睾丸肿瘤病因学中的作用。

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引用本文的文献

1
Birth dates of men with cancer of the testis.睾丸癌男性患者的出生日期。
J Epidemiol Community Health. 1985 Sep;39(3):237-43. doi: 10.1136/jech.39.3.237.

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