Chaaya Gerard, Morales Jorge, Castiglioni Analia, Subhani Noman, Asmar Abdo
University of Central Florida College of Medicine, Orlando, Florida.
University of Central Florida College of Medicine, Orlando, Florida; Orlando VA Medical Center, Orlando, Florida.
Am J Med Sci. 2018 Feb;355(2):191-194. doi: 10.1016/j.amjms.2017.03.037. Epub 2017 Apr 8.
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.
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。