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
{"title":"遗传性癌症易感综合征中的妇科病变。","authors":"Pavel Dundr,&nbsp;David Cibula,&nbsp;Lenka Foretová,&nbsp;Milan Macek,&nbsp;Kateřina Kopečková,&nbsp;Luboš Petruželka,&nbsp;Kristýna Němejcová,&nbsp;Michaela Bártů,&nbsp;Jan Hojný,&nbsp;Nikola Hájková,&nbsp;Radek Jakša,&nbsp;Pavol Janega,&nbsp;Ivana Stružinská","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":9861,"journal":{"name":"Ceskoslovenska patologie","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Gynecological lesions in hereditary cancer predisposition syndromes.\",\"authors\":\"Pavel Dundr,&nbsp;David Cibula,&nbsp;Lenka Foretová,&nbsp;Milan Macek,&nbsp;Kateřina Kopečková,&nbsp;Luboš Petruželka,&nbsp;Kristýna Němejcová,&nbsp;Michaela Bártů,&nbsp;Jan Hojný,&nbsp;Nikola Hájková,&nbsp;Radek Jakša,&nbsp;Pavol Janega,&nbsp;Ivana Stružinská\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":9861,\"journal\":{\"name\":\"Ceskoslovenska patologie\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Ceskoslovenska patologie\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ceskoslovenska patologie","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
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。
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Ceskoslovenska patologie
Ceskoslovenska patologie Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
17
期刊最新文献
Histopathology of skin melanocytic lesions. Changes in the diagnosis of thyroid tumours in the 5th edition of the WHO classification of endocrine neoplasms. Parathyroid tumors in the 5th edition of the WHO Classification of Tumors of the Endocrine Organs. Changes in thyroid cytology reporting in the 3rd edition of the Bethesda system. Clinical, Morphological and Molecular Features of Spitz tumors.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1