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MON-LB063 Pheochromocytoma Presenting as Fulminant Renal Failure with Hemolytic Anemia in a Young Male

Background Pheochromocytoma is a rare catecholamine-secreting tumor of the adrenal chromaffin cells. Historically, these tumors have been described by the classic triad of paroxysmal tachycardia, diaphoresis and headaches in the setting of uncontrolled hypertension. However, most patients do not man...

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Detalhes bibliográficos
Publicado no:J Endocr Soc
Main Authors: Ravi, Divya, Sharma, Nishant, Rajagopalan, Sharath, Bukenova, Lidiya
Formato: Artigo
Idioma:Inglês
Publicado em: Endocrine Society 2019
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6550794/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-MON-LB063
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