Pheochromocytoma: A Rare Presentation.

Robert T Emery, Hunter L Brown, Katherine Q Emery, J R Baker
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Abstract

Pheochromocytoma is a very rare neuroendocrine tumor usually located in one or both adrenal glands with an incidence of about 4 per 1,000,000 and about 1000 diagnosed per year. Pheochromocytomas can be located in extra-adrenal locations with about 1% being located in the urinary bladder.(1) We describe the presentation, diagnosis and treatment of one of these extremely rare tumors in the bladder.

嗜铬细胞瘤:一种罕见的表现。
嗜铬细胞瘤是一种非常罕见的神经内分泌肿瘤,通常位于一个或两个肾上腺,发病率约为100万分之4,每年诊断约1000例。嗜铬细胞瘤可位于肾上腺外,约1%位于膀胱。(1)我们描述了一种极其罕见的膀胱肿瘤的表现,诊断和治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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