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 of VHL syndrome patients.

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

Landoni, L;Scardoni, M;Piredda, M L;Cingarlini, S;Scarpa, A;D'Onofrio, M;Girelli, D;
2021

Abstract

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 of VHL syndrome patients.
Clinical presentation; Genotype–phenotype correlations; Pancreatic neuroendocrine tumors; Von Hippel–Lindau syndrome
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/1043979
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