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Cancer surveillance for transgender and gender diverse patients with Lynch syndrome: a practice resource of the Collaborative Group of the Americas on Inherited Gastrointestinal Cancer
Familial Cancer ( IF 2.2 ) Pub Date : 2023-06-21 , DOI: 10.1007/s10689-023-00341-4
Rachel Hodan 1 , Linda Rodgers-Fouche 2 , Anu Chittenden 3 , Mev Dominguez-Valentin 4 , James Ferriss 5 , Lauren Gima 6 , Ole-Petter R Hamnvik 7 , Gregory E Idos 8 , Kevin Kline 9 , Diane R Koeller 3 , Jessica M Long 10 , Danielle McKenna 10 , Charles Muller 11 , Maxton Thoman 12 , Anton Wintner 12 , Bronwyn S Bedrick 13 ,
Affiliation  

Transgender and gender diverse (TGD) populations with hereditary cancer syndromes face unique obstacles to identifying and obtaining appropriate cancer surveillance and risk-reducing procedures. There is a lack of care provider knowledge about TGD health management. Lynch syndrome (LS) is one of the most common hereditary cancer syndromes, affecting an estimated 1 in 279 individuals. There are no clinical guidelines specific for TGD individuals with LS, highlighting a need to improve the quality of care for this population. There is an urgent need for cancer surveillance recommendations for TGD patients. This commentary provides recommendations for cancer surveillance, risk-reducing strategies, and genetic counseling considerations for TGD patients with LS.



中文翻译:

林奇综合征跨性别和性别多样化患者的癌症监测:美洲遗传性胃肠癌合作小组的实践资源

患有遗传性癌症综合征的跨性别和性别多样化 (TGD) 人群在识别和获得适当的癌症监测和降低风险程序方面面临着独特的障碍。护理人员缺乏有关 TGD 健康管理的知识。林奇综合征 (LS) 是最常见的遗传性癌症综合征之一,估计每 279 人中就有 1 人患有林奇综合征。目前尚无专门针对患有 LS 的 TGD 个体的临床指南,强调需要提高该人群的护理质量。迫切需要针对 TGD 患者的癌症监测建议。本评论为患有 LS 的 TGD 患者提供癌症监测、降低风险策略和遗传咨询注意事项的建议。

更新日期:2023-06-21
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