Clinical, Diagnostic, and Treatment Characteristics of SDHA-Related Metastatic Pheochromocytoma and Paraganglioma

Background: Pheochromocytoma and paraganglioma (PHEO/PGL) are rare neuroendocrine tumors which may cause potentially life-threatening complications, with about a third of cases found to harbor specific gene mutations. Thus, early diagnosis, treatment, and meticulous monitoring are of utmost importan...

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Detalles Bibliográficos
Autores principales: Jha, Abhishek, de Luna, Kristine, Balili, Charlene Ann, Millo, Corina, Paraiso, Cecilia Angela, Ling, Alexander, Gonzales, Melissa K., Viana, Bruna, Alrezk, Rami, Adams, Karen T., Tena, Isabel, Chen, Alice, Neuzil, Jiri, Raygada, Margarita, Kebebew, Electron, Taieb, David, O'Dorisio, M. Sue, O'Dorisio, Thomas, Civelek, Ali Cahid, Stratakis, Constantine A., Mercado-Asis, Leilani, Pacak, Karel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Oncology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395427/
https://www.ncbi.nlm.nih.gov/pubmed/30854332
http://dx.doi.org/10.3389/fonc.2019.00053

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395427/
https://www.ncbi.nlm.nih.gov/pubmed/30854332
http://dx.doi.org/10.3389/fonc.2019.00053

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