Pheochromocytomas and Paragangliomas: From Genetic Diversity to Targeted Therapies

Pheochromocytoma and paraganglioma (PCPGs) are rare neuroendocrine tumors that arise from the chromaffin tissue of adrenal medulla and sympathetic ganglia. Although metastatic PCPGs account for only 10% of clinical cases, morbidity and mortality are high because of the uncontrollable mass effect and...

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Detalles Bibliográficos
Autores principales: Pang, Ying, Liu, Yang, Pacak, Karel, Yang, Chunzhang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521122/
https://www.ncbi.nlm.nih.gov/pubmed/30925729
http://dx.doi.org/10.3390/cancers11040436

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521122/
https://www.ncbi.nlm.nih.gov/pubmed/30925729
http://dx.doi.org/10.3390/cancers11040436

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