| Literature DB >> 29406048 |
Gerard Chaaya1, Jorge Morales1, Analia Castiglioni2, Noman Subhani3, Abdo Asmar4.
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. Published by Elsevier Inc.Entities:
Keywords: Bladder; Hypertension; Paraganglioma; Pheochromocytoma; Urinary tract infection
Mesh:
Year: 2017 PMID: 29406048 DOI: 10.1016/j.amjms.2017.03.037
Source DB: PubMed Journal: Am J Med Sci ISSN: 0002-9629 Impact factor: 2.378