Somatic VHL Mutation in a Patient With MEN1-Associated Metastatic Pancreatic Neuroendocrine Tumor Responding to Sunitinib Treatment: A Case Report

Multiple endocrine neoplasia type 1 (MEN1) and von Hippel-Lindau (VHL) are autosomal-dominant diseases caused by germline mutations in tumor-suppressor genes. A patient with a germline MEN1 mutation and a somatic VHL mutation in the tumor has not been reported. Herein, we report on a patient with ME...

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Detalles Bibliográficos
Autores principales: Shell, Jasmine, Patel, Dhaval, Powers, Astin, Quezado, Martha, Killian, Keith, Meltzer, Paul, Zhu, Jack, Gaitanidis, Apostolos, Karzai, Fatima, Neychev, Vladimir, Green, Patience, Kebebew, Electron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2017
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686673/
https://www.ncbi.nlm.nih.gov/pubmed/29264567
http://dx.doi.org/10.1210/js.2017-00156

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