Cargando…
How Many Times Can One Go Back to the Drawing Board before the Accurate Diagnosis and Surgical Treatment of Glucagonoma?
Glucagonomas are neuroendocrine tumors (NETs) that arise from the alpha cells of the pancreatic islets. They are typically slow-growing tumors associated with abnormal glucagon secretion, resulting in one or more non-specific clinical features, such as necrolytic migratory erythema (NME), diabetes,...
Autores principales: | Martin, Carmen Sorina, Parfeni, Ovidiu Dumitru, Popa, Liliana Gabriela, Mihai, Mara Madalina, Terzea, Dana, Herlea, Vlad, Gherghe, Mirela, Adam, Razvan, Alnuaimi, Osama, Calu, Valentin, Miron, Adrian, Negoita, Silvius, Nitipir, Cornelia, Fica, Simona |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774529/ https://www.ncbi.nlm.nih.gov/pubmed/35054383 http://dx.doi.org/10.3390/diagnostics12010216 |
Ejemplares similares
-
Somatostatinoma and Neurofibromatosis Type 1-A Case Report and Review of the Literature
por: Martin, Sorina, et al.
Publicado: (2020) -
Insights into Epigenetic Changes Related to Genetic Variants and Cells-of-Origin of Pancreatic Neuroendocrine Tumors: An Algorithm for Practical Workup
por: Ciobanu, Oana A., et al.
Publicado: (2022) -
Glucagonoma and Glucagonoma Syndrome: One Center's Experience of Six Cases
por: Wei, Jishu, et al.
Publicado: (2018) -
Hereditary leiomyomatosis and renal cell cancer syndrome – case report and review of the literature
por: Popa, Liliana Gabriela, et al.
Publicado: (2020) -
Glucagonoma and Glucagonoma Syndrome: A Case Report with Review of Recent Advances in Management
por: Al-Faouri, Ashraf, et al.
Publicado: (2016)