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MON-LB041 Pheochromocytoma - Illusive Myriad of Symptoms

Background: Pheochromocytoma is a rare neuroendocrine neoplasm arising from the adrenal medullary chromaffin cells. It contributes to 80-85% of catecholamine secreting tumors. The annual incidence of pheochromocytoma is 0.8 cases per 100,000 person-years. It can be both sporadic or familial. The cla...

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Bibliografski detalji
Izdano u:J Endocr Soc
Glavni autori: Gunda, Mouna, Bantu, Sravani, Jakka, Bharath, Thudi, Vaishali
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2020
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7209449/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.2030
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