膀胱嗜铬细胞瘤

Pheochromocytoma of the bladder.

作者信息

Williams Paige, Siref Larry, Feloney Mike

机构信息

The authors practice at CHI Health Alegent Creighton Clinic Urology in Omaha, Neb. Dr. Siref also is program director of the urologic surgery residency program and an associate professor in the Section of Urologic Surgery at Creighton University School of Medicine in Omaha. Dr. Feloney also is chief of the Division of Urology and an associate professor in the Department of Surgery at Creighton University School of Medicine and practices at the VA Nebraska-Western Iowa Healthcare System. The authors have disclosed no potential conflicts of interest, financial or otherwise.

出版信息

JAAPA. 2017 Oct;30(10):23-25. doi: 10.1097/01.JAA.0000522134.68445.50.

DOI:10.1097/01.JAA.0000522134.68445.50

PMID:28953019

Abstract

Pheochromocytoma is a rare catecholamine-secreting tumor. Unless recognized and treated appropriately it can be lethal. Common symptoms include sustained or paroxysmal hypertension associated with headaches, sweating, or palpitations. This article describes a patient with an extra-adrenal pheochromocytoma who presented with symptoms associated with voiding.

摘要

嗜铬细胞瘤是一种罕见的分泌儿茶酚胺的肿瘤。除非得到正确的诊断和治疗，否则它可能是致命的。常见症状包括与头痛、出汗或心悸相关的持续性或阵发性高血压。本文描述了一名患有肾上腺外嗜铬细胞瘤的患者，其表现出与排尿相关的症状。