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膀胱副神经节瘤:高血压和尿路感染的罕见病因

Paraganglioma of the Urinary Bladder: A Rare Cause of Hypertension and Urinary Tract Infections.

作者信息

Chaaya Gerard, Morales Jorge, Castiglioni Analia, Subhani Noman, Asmar Abdo

机构信息

University of Central Florida College of Medicine, Orlando, Florida.

University of Central Florida College of Medicine, Orlando, Florida; Orlando VA Medical Center, Orlando, Florida.

出版信息

Am J Med Sci. 2018 Feb;355(2):191-194. doi: 10.1016/j.amjms.2017.03.037. Epub 2017 Apr 8.

Abstract

Pheochromocytoma is a neoplasm, which develops from cells of the chromaffin tissues that are derived from the ectodermic neural system and mostly situated within the adrenal medulla. Approximately 15% of pheochromocytoma cases arise from extra-adrenal chromaffin tissue. Pheochromocytoma of the bladder is rare and accounts for less than 0.06% of all bladder neoplasms and less than 1% of all pheochromocytomas. We report a case of a young woman who presented with uncontrolled hypertension, recurrent urinary tract infections and micturition attacks and was found to have a metastatic bladder paraganglioma. In addition, we provide a summary table of the clinical manifestations of paragangliomas based on anatomic locations.

摘要

嗜铬细胞瘤是一种肿瘤,它由起源于外胚层神经系统的嗜铬组织细胞发展而来,大多位于肾上腺髓质内。约15%的嗜铬细胞瘤病例起源于肾上腺外嗜铬组织。膀胱嗜铬细胞瘤罕见,占所有膀胱肿瘤的比例不到0.06%,占所有嗜铬细胞瘤的比例不到1%。我们报告一例年轻女性病例,该患者出现难以控制的高血压、复发性尿路感染和排尿发作,经检查发现患有转移性膀胱副神经节瘤。此外,我们还提供了一份基于解剖位置的副神经节瘤临床表现汇总表。

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