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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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| Publicat a: | J Endocr Soc |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Endocrine Society
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6551010/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-MON-383 |
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