Recurrent Pheochromocytoma, as Component of Multiple Endocrine Neoplasia

Background: Pheochromocytoma is a rare neuroendocrine tumor from the adrenal medulla’s chromaffin cells that secrete catecholamines. The mainstay of treatment is surgery. Although rare, it has a recurrence rate of 6.5-16.5% even after adequate surgical removal with a notable increase in prevalence a...

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Detaylı Bibliyografya
Yayımlandı:J Endocr Soc
Asıl Yazarlar: Dominguez, Hydelene Beray, Pacheco, Elizabeth P, Jimeno, Cecilia, Lantion-Ang, Franceslina C, Hernandez, Edrome, Chiu, Harold Henrison Chang
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2021
Konular:
Tumor Biology
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC8089295/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvab048.2055
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