A Direct Comparison of Patients With Hereditary and Sporadic Pancreatic Neuroendocrine Tumors: Evaluation of Clinical Course, Prognostic Factors and Genotype–Phenotype Correlations

A Direct Comparison of Patients With Hereditary and Sporadic Pancreatic Neuroendocrine Tumors: Evaluation of Clinical Course, Prognostic Factors and Genotype–Phenotype Correlations

IntroductionPancreatic neuroendocrine tumors (PNETs) in hereditary syndromes pose a significant challenge to clinicians. The rarity of these syndromes and PNETs itself make it difficult to directly compare them with sporadic PNETs. Despite research suggesting differences between these two entities,...

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Bibliographic Details
Main Authors: Przemysław Soczomski, Beata Jurecka-Lubieniecka, Aleksandra Krzywon, Alexander Jorge Cortez, Stanisław Zgliczynski, Natalia Rogozik, Małgorzata Oczko-Wojciechowska, Agnieszka Pawlaczek, Tomasz Bednarczuk, Barbara Jarzab
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Endocrinology
Subjects:
multiple neuroendocrine neoplasia type 1
Von Hippel–Lindau Syndrome
pancreatic neuroendocrine tumor
hereditary pancreatic neuroendocrine tumor (PNET)
comparison
genotype-phenotype correlation
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2021.681013/full

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https://www.frontiersin.org/articles/10.3389/fendo.2021.681013/full

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