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

INTRODUCTION: Pancreatic 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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Detalles Bibliográficos
Autores principales: Soczomski, Przemysław, Jurecka-Lubieniecka, Beata, Krzywon, Aleksandra, Cortez, Alexander Jorge, Zgliczynski, Stanisław, Rogozik, Natalia, Oczko-Wojciechowska, Małgorzata, Pawlaczek, Agnieszka, Bednarczuk, Tomasz, Jarzab, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8194819/
https://www.ncbi.nlm.nih.gov/pubmed/34122352
http://dx.doi.org/10.3389/fendo.2021.681013

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8194819/
https://www.ncbi.nlm.nih.gov/pubmed/34122352
http://dx.doi.org/10.3389/fendo.2021.681013

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