Metachronous colorectal carcinoma with massive submucosal invasion detected by annual surveillance in a Lynch syndrome patient: a case report

BACKGROUND: Lynch syndrome is the most common form of hereditary colorectal carcinoma. It is characterized by the presence of germline mutations in DNA mismatch repair genes. Mutation carriers have a lifetime risk of developing colorectal carcinoma of approximately 80%. Current treatment guidelines...

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Detalles Bibliográficos
Autores principales: Utsumi, Masashi, Tanakaya, Kohji, Mushiake, Yutaka, Kunitomo, Tomoyoshi, Yasuhara, Isao, Taniguchi, Fumitaka, Arata, Takashi, Katsuda, Koh, Aoki, Hideki, Takeuchi, Hitoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5540342/
https://www.ncbi.nlm.nih.gov/pubmed/28764791
http://dx.doi.org/10.1186/s12957-017-1207-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5540342/
https://www.ncbi.nlm.nih.gov/pubmed/28764791
http://dx.doi.org/10.1186/s12957-017-1207-3

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