Lynch Syndrome-Associated Endometrial Cancer With Combined EPCAM-MSH2 Deletion: A Case Report

BACKGROUND: Lynch syndrome (LS), an autosomal dominant disorder, is characterized by germline pathogenic variants in DNA mismatch repair (MMR) genes like MSH2. EPCAM deletions cause a minority (3%) of LS cases. However, there are only a few reports of LS-associated endometrial cancer (LS-EC) induced...

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Detalles Bibliográficos
Autores principales: Huang, Rong, Deng, Xiangyu, Zhang, Zhenhua, Wen, Qinglian, Li, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Oncology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931483/
https://www.ncbi.nlm.nih.gov/pubmed/35311082
http://dx.doi.org/10.3389/fonc.2022.856452

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931483/
https://www.ncbi.nlm.nih.gov/pubmed/35311082
http://dx.doi.org/10.3389/fonc.2022.856452

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