MON-383 Sporadic Bilateral Pheochromocytoma with Renal Pelvis Paraganglioma: A Rare Coexisting Occurrence

Pheochromocytomas (PHEO) and paragangliomas (PGL) are rare neuroendocrine catecholamine-secreting tumors that arise from chromaffin cells of the adrenal medulla and the extra-adrenal autonomic paraglanglia respectively. The natural course of this disease increases morbidity and mortality. Most cases...

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Detalles Bibliográficos
Autores principales: Pirela, Daniela, Abraham, Rtika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Adrenal
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551010/
http://dx.doi.org/10.1210/js.2019-MON-383

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551010/
http://dx.doi.org/10.1210/js.2019-MON-383

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