Clinical presentation, genotype–phenotype correlations, and outcome of pancreatic neuroendocrine tumors in Von Hippel–Lindau syndrome

PURPOSE: Data regarding the clinical management and follow-up of pancreatic neuroendocrine tumors (PanNETs) associated with Von Hippel–Lindau (VHL) syndrome are limited. This study aimed to assess clinical presentation, genotype–phenotype correlations, treatment and prognosis of PanNETs in a series...

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Detalles Bibliográficos
Autores principales: Penitenti, F., Landoni, L., Scardoni, M., Piredda, M. L., Cingarlini, S., Scarpa, A., D’Onofrio, M., Girelli, D., Davi, M. V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440302/
https://www.ncbi.nlm.nih.gov/pubmed/34036514
http://dx.doi.org/10.1007/s12020-021-02752-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8440302/
https://www.ncbi.nlm.nih.gov/pubmed/34036514
http://dx.doi.org/10.1007/s12020-021-02752-8

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