Diagnosis and treatment of neuroendocrine tumors – A series of 13 clinical cases (2014–2017)

Paragangliomas and pheocromocytomas are rare neuroendocrine tumors with different clinical presentation, being responsible for secondary arterial hypertension with target-organ lesions. Surgery is a curative therapy in these tumors and demands a multidisciplinary approach. These tumors are more freq...

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Detalles Bibliográficos
Autores principales: Sepúlveda Santos, Tiago, Figueira, Alberto, Rocha, José, Coutinho, João, Carvalho, Leonor, Ducla-Soares, J.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803053/
https://www.ncbi.nlm.nih.gov/pubmed/33447750
http://dx.doi.org/10.1016/j.ijchy.2019.100019

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7803053/
https://www.ncbi.nlm.nih.gov/pubmed/33447750
http://dx.doi.org/10.1016/j.ijchy.2019.100019

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