Multiple endocrine neoplasia type 1 combined with thyroid neoplasm: A case report and review of literatures

BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a rare hereditary tumor syndrome inherited in an autosomal dominant manner and presents mostly as parathyroid, endocrine pancreas (such as gastrinoma) and anterior pituitary tumors. At present, papillary thyroid carcinoma (PTC) and nodular go...

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Detalles Bibliográficos
Autores principales: Xu, Jia-Lu, Dong, Su, Sun, Le-Le, Zhu, Jin-Xin, Liu, Jia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790451/
https://www.ncbi.nlm.nih.gov/pubmed/35127917
http://dx.doi.org/10.12998/wjcc.v10.i3.1032

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8790451/
https://www.ncbi.nlm.nih.gov/pubmed/35127917
http://dx.doi.org/10.12998/wjcc.v10.i3.1032

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