Hereditary oral squamous cell carcinoma associated with CDKN2A germline mutation: a case report

BACKGROUND: Germline CDKN2A mutations are a well-known cause of familial atypical multiple mole melanoma (OMIM #155601) and melanoma-pancreatic cancer syndrome (OMIM #606719). Increased risk of head and neck squamous cell carcinoma (HNSCC), particularly oral squamous cell carcinoma (OSCC) in those w...

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Detalles Bibliográficos
Autores principales: Jeong, Ah-Reum, Forbes, Kimberly, Orosco, Ryan K., Cohen, Ezra E. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8818223/
https://www.ncbi.nlm.nih.gov/pubmed/35123577
http://dx.doi.org/10.1186/s40463-022-00556-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8818223/
https://www.ncbi.nlm.nih.gov/pubmed/35123577
http://dx.doi.org/10.1186/s40463-022-00556-y

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