Emery Robert T, Brown Hunter L, Emery Katherine Q, Baker J R
J Ark Med Soc. 2017 Feb;113(8):188-190.
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.
嗜铬细胞瘤是一种非常罕见的神经内分泌肿瘤，通常位于一侧或双侧肾上腺，发病率约为每100万人中有4例，每年约有1000例被诊断出来。嗜铬细胞瘤也可位于肾上腺外，约1%位于膀胱。（1）我们描述了一例膀胱内这种极其罕见肿瘤的临床表现、诊断及治疗过程。
