Incidental Pheochromocytoma: Silent but Violent

Background: Pheochromocytoma is a rare catecholamine secreting neuroendocrine tumor. It arises from the chromaffin cells of adrenal medulla. It is diagnosed in 5–6.5% of adrenal incidentalomas which is not common. The usual clinical presentation includes the classic triad of sweating, headache and t...

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Bibliographic Details
Published in:J Endocr Soc
Main Authors: Bantu, Sravani, Vallepu, Shirisha R, Gunda, Mouna, Thudi, Vaishali
Format: Artigo
Language:Inglês
Published: Oxford University Press 2021
Subjects:
Adrenal
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC8089244/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvab048.277
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