Multiple endocrine neoplasia type 1 involving both the liver and lung: a case report

BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant tumor syndrome with a high degree of heterogeneity in clinical phenotypes, generally involving the parathyroid, anterior pituitary, and enteropancreas. In recent years, several new insights into the clinical features...

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Detalles Bibliográficos
Autores principales: Lai, Jianlin, Huang, Yangyang, Wu, Junyi, Cheng, Hui, Qiu, Funan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088025/
https://www.ncbi.nlm.nih.gov/pubmed/35538538
http://dx.doi.org/10.1186/s12957-022-02622-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9088025/
https://www.ncbi.nlm.nih.gov/pubmed/35538538
http://dx.doi.org/10.1186/s12957-022-02622-1

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