Myxofibrosarcoma harboring an MLH1 pathogenic germline variant associated with Muir-Torre syndrome: a case report

BACKGROUND: Muir–Torre syndrome (MTS), which accounts for a small subset (1–3 %) of Lynch syndrome (LS), is an autosomal dominant genetic disorder characterized by sebaceous gland or keratoacanthoma associated with visceral malignancies. Most families with MTS have pathogenic germline variants (PGV)...

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Detalles Bibliográficos
Autores principales: Nakagawa, Makoto, Kobayashi, Eisuke, Yamada, Masayoshi, Watanabe, Tomoko, Hirata, Makoto, Tanabe, Noriko, Ushiama, Mineko, Sakamoto, Hiromi, Sato, Chiaki, Mori, Taisuke, Yoshida, Akihiko, Yoshida, Teruhiko, Sugano, Kokichi, Kawai, Akira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379813/
https://www.ncbi.nlm.nih.gov/pubmed/34419117
http://dx.doi.org/10.1186/s13053-021-00192-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379813/
https://www.ncbi.nlm.nih.gov/pubmed/34419117
http://dx.doi.org/10.1186/s13053-021-00192-z

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