A case of Turcot’s syndrome type 1 with loss of immunoexpression of MSH6 in colon cancer and liver metastasis due to secondary somatic mutation in coding mononucleotide (C)8 tract: a case report

BACKGROUND: Lynch syndrome (LS), which is known as a hereditary cancer syndrome, is distinguished by microsatellite instability, represented by the altered number of repetitive sequences in the coding and/or non-coding region. Immunohistochemical staining (IHC) of DNA mismatch repair (MMR) proteins...

Descripción completa

Detalles Bibliográficos
Autores principales: Akabane, Shintaro, Hinoi, Takao, Akagi, Kiwamu, Yamamoto, Hideki, Sada, Haruki, Shimizu, Yosuke, Shimizu, Wataru, Sudo, Takeshi, Onoe, Takashi, Ishiyama, Kohei, Suzuki, Takahisa, Tazawa, Hirofumi, Hadano, Naoto, Misumi, Toshihiro, Kojima, Masato, Kubota, Haruna, Taniyama, Daiki, Kuraoka, Kazuya, Tashiro, Hirotaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7345515/
https://www.ncbi.nlm.nih.gov/pubmed/32611331
http://dx.doi.org/10.1186/s12881-020-01079-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7345515/
https://www.ncbi.nlm.nih.gov/pubmed/32611331
http://dx.doi.org/10.1186/s12881-020-01079-x

Ejemplares similares