一名李-弗劳米尼综合征患者的眼附件皮脂腺癌。

Pub Date : 2024-07-29 DOI:10.1080/01676830.2024.2382268
Chia W Hsu, Cornelia W Peterson, Charles G Eberhart, Christian F Meyer, Deborah K Armstrong, Katie Fiallos, Ashley A Campbell
{"title":"一名李-弗劳米尼综合征患者的眼附件皮脂腺癌。","authors":"Chia W Hsu, Cornelia W Peterson, Charles G Eberhart, Christian F Meyer, Deborah K Armstrong, Katie Fiallos, Ashley A Campbell","doi":"10.1080/01676830.2024.2382268","DOIUrl":null,"url":null,"abstract":"<p><p>Li-Fraumeni syndrome (LFS) is caused by a pathogenic germline variant at the <i>TP53</i> locus and is associated with an increased predisposition to a variety of cancers. The neoplasms most frequently associated with LFS are sarcomas, breast cancer, brain tumors, and adrenocortical carcinomas. In this case report, we present a 43-year-old male diagnosed with an ocular adnexal sebaceous carcinoma of the right upper eyelid who was confirmed to have LFS with subsequent genetic testing. The mutational profile of both the patient's genetic screen and tumor sequencing were congruent, demonstrating the same pathogenic loss-of-function <i>TP53</i> variant. This case report highlights the importance of pursuing genetic testing in patients with a history of multiple tumor types, particularly those with uncommon diagnoses. In this case, confirmation of LFS had important implications for personalized patient care, including identification of contraindicated treatment interventions and the imaging modalities necessary for vigilant follow-up screening.</p>","PeriodicalId":0,"journal":{"name":"","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ocular adnexal sebaceous carcinoma in a patient with Li-Fraumeni syndrome.\",\"authors\":\"Chia W Hsu, Cornelia W Peterson, Charles G Eberhart, Christian F Meyer, Deborah K Armstrong, Katie Fiallos, Ashley A Campbell\",\"doi\":\"10.1080/01676830.2024.2382268\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Li-Fraumeni syndrome (LFS) is caused by a pathogenic germline variant at the <i>TP53</i> locus and is associated with an increased predisposition to a variety of cancers. The neoplasms most frequently associated with LFS are sarcomas, breast cancer, brain tumors, and adrenocortical carcinomas. In this case report, we present a 43-year-old male diagnosed with an ocular adnexal sebaceous carcinoma of the right upper eyelid who was confirmed to have LFS with subsequent genetic testing. The mutational profile of both the patient's genetic screen and tumor sequencing were congruent, demonstrating the same pathogenic loss-of-function <i>TP53</i> variant. This case report highlights the importance of pursuing genetic testing in patients with a history of multiple tumor types, particularly those with uncommon diagnoses. In this case, confirmation of LFS had important implications for personalized patient care, including identification of contraindicated treatment interventions and the imaging modalities necessary for vigilant follow-up screening.</p>\",\"PeriodicalId\":0,\"journal\":{\"name\":\"\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0,\"publicationDate\":\"2024-07-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/01676830.2024.2382268\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/01676830.2024.2382268","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

Li-Fraumeni 综合征(LFS)是由 TP53 基因座上的致病性种系变异引起的,与易患多种癌症有关。最常与 LFS 相关的肿瘤是肉瘤、乳腺癌、脑肿瘤和肾上腺皮质癌。在本病例报告中,我们介绍了一名被诊断为右上眼睑眼附属皮脂腺癌的 43 岁男性患者,他在随后的基因检测中被证实患有 LFS。患者基因筛查和肿瘤测序的突变特征一致,显示出相同的致病性功能缺失 TP53 变异。本病例报告强调了对有多种肿瘤病史的患者进行基因检测的重要性,尤其是那些诊断不常见的患者。在本病例中,LFS 的确认对患者的个性化治疗具有重要意义,包括确定禁忌的治疗干预措施和警惕随访筛查所需的成像模式。
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
查看原文
Ocular adnexal sebaceous carcinoma in a patient with Li-Fraumeni syndrome.

Li-Fraumeni syndrome (LFS) is caused by a pathogenic germline variant at the TP53 locus and is associated with an increased predisposition to a variety of cancers. The neoplasms most frequently associated with LFS are sarcomas, breast cancer, brain tumors, and adrenocortical carcinomas. In this case report, we present a 43-year-old male diagnosed with an ocular adnexal sebaceous carcinoma of the right upper eyelid who was confirmed to have LFS with subsequent genetic testing. The mutational profile of both the patient's genetic screen and tumor sequencing were congruent, demonstrating the same pathogenic loss-of-function TP53 variant. This case report highlights the importance of pursuing genetic testing in patients with a history of multiple tumor types, particularly those with uncommon diagnoses. In this case, confirmation of LFS had important implications for personalized patient care, including identification of contraindicated treatment interventions and the imaging modalities necessary for vigilant follow-up screening.

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
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信