遗传性癌症易感综合征中的妇科病变。

Q4 Medicine
Ceskoslovenska patologie Pub Date : 2021-01-01
Pavel Dundr, David Cibula, Lenka Foretová, Milan Macek, Kateřina Kopečková, Luboš Petruželka, Kristýna Němejcová, Michaela Bártů, Jan Hojný, Nikola Hájková, Radek Jakša, Pavol Janega, Ivana Stružinská
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引用次数: 0

摘要

可能表现为女性内生殖道的遗传性肿瘤综合征是一类异质性疾病。最常见的两种疾病是遗传性乳腺癌和卵巢癌综合征,以及林奇综合征。较不常见的综合征包括横纹肌样肿瘤易感综合征、考登综合征、结节性硬化症、DICER1综合征、痣状基底细胞癌综合征、Peutz-Jeghers综合征、von Hippel-Lindau病、遗传性平滑肌瘤病和肾细胞癌综合征。该手稿的目的是提供一个全面的概述,这些遗传性肿瘤综合征,可以表现在女性生殖系统的领域,重点是总结,肿瘤的特点,可以发展与这些综合征,并采取预防性切除的组织和器官的处理方法。本文还讨论了Lynch综合征的筛查问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gynecological lesions in hereditary cancer predisposition syndromes.

Hereditary tumor syndromes with a possible manifestation in the female internal genital tract represent a heterogeneous group of diseases. The two most common entities are the hereditary breast and ovarian cancer syndrome, and the Lynch syndrome. The less common syndromes include the rhabdoid tumor predisposition syndrome, Cowden syndrome, tuberous sclerosis complex, DICER1 syndrome, nevoid basal cell carcinoma syndrome, Peutz-Jeghers syndrome, von Hippel-Lindau disease, and hereditary leiomyomatosis and renal cell cancer syndrome. The goal of this manuscript is to provide a comprehensive overview of those hereditary tumor syndromes which can manifest in the area of the female genital system, with an emphasis on their summary, the characteristics of the tumors which can develop in association with these syndromes, and the approach to the processing of prophylactically removed tissues and organs. The issue of Lynch syndrome screening is also discussed.

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来源期刊
Ceskoslovenska patologie
Ceskoslovenska patologie Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
17
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