Late onset asymptomatic pancreatic neuroendocrine tumor – A case report on the phenotypic expansion for MEN1

BACKGROUND: Multiple endocrine neoplasia type 1 (MEN1) is a hereditary cancer syndrome associated with several endocrine as well as non-endocrine tumors and is caused by mutations in the MEN1 gene. Primary hyperparathyroidism affects the majority of MEN1 individuals by age 50 years. Additionally, ME...

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Detalles Bibliográficos
Autores principales: Kaiwar, Charu, Macklin, Sarah K., Gass, Jennifer M., Jackson, Jessica, Klee, Eric W., Hines, Stephanie L., Stauffer, John A., Atwal, Paldeep S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5521080/
https://www.ncbi.nlm.nih.gov/pubmed/28736585
http://dx.doi.org/10.1186/s13053-017-0070-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5521080/
https://www.ncbi.nlm.nih.gov/pubmed/28736585
http://dx.doi.org/10.1186/s13053-017-0070-0

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