De novo familial adenomatous polyposis associated thyroid cancer with a c.2929delG frameshift deletion mutation in APC: a case report and literature review

BACKGROUND: Germline mutations in the APC gene located on chromosome 5q 21–22 can lead to familial adenomatous polyposis (FAP) and the development of colorectal cancer (CRC) if left untreated. As a rare extracolonic manifestation, thyroid cancer is diagnosed in about 2.6% of FAP patients. The genoty...

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Detalles Bibliográficos
Autores principales: Xu, Miaorong, Zheng, Yuyan, Zuo, Zhongchao, Zhou, Qin, Deng, Qun, Wang, Jianwei, Wang, Da
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979514/
https://www.ncbi.nlm.nih.gov/pubmed/36864485
http://dx.doi.org/10.1186/s12957-023-02951-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979514/
https://www.ncbi.nlm.nih.gov/pubmed/36864485
http://dx.doi.org/10.1186/s12957-023-02951-9

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