Pheochromocytomas and Paragangliomas: New Developments with Regard to Classification, Genetics, and Cell of Origin

Pheochromocytomas (PCC) and paragangliomas (PGL) are rare neuroendocrine tumors that arise in the adrenal medulla and in extra-adrenal locations, such as the head, neck, thorax, abdomen, and pelvis. Classification of these tumors into those with or without metastatic potential on the basis of gross...

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Detalles Bibliográficos
Autores principales: Koopman, Karen, Gaal, Jose, de Krijger, Ronald R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721302/
https://www.ncbi.nlm.nih.gov/pubmed/31362359
http://dx.doi.org/10.3390/cancers11081070

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721302/
https://www.ncbi.nlm.nih.gov/pubmed/31362359
http://dx.doi.org/10.3390/cancers11081070

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