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.
Original language | English (US) |
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Pages (from-to) | 191-194 |
Number of pages | 4 |
Journal | American Journal of the Medical Sciences |
Volume | 355 |
Issue number | 2 |
DOIs | |
State | Published - Feb 2018 |
Keywords
- Bladder
- Hypertension
- Paraganglioma
- Pheochromocytoma
- Urinary tract infection
ASJC Scopus subject areas
- General Medicine