| Literature DB >> 35371661 |
Bindu Rajkumar1, Rishabh Sahai2, Dezy Singh3, Monika Singh1, Ashok Singh1, Arvind Kumar1.
Abstract
Pheochromocytomas are tumors arising from catecholamine secreting cells of adrenal glands. Extra adrenal gland pheochromocytomas are called paragangliomas. They account for 15% of all pheochromocytomas. Paraganglioma arising in the urinary bladder is extremely rare accounting for 0.06% of all urinary bladder tumor cases. We present a case of a 55-year-old female patient who complained of pain in abdomen and intermittent haematuria subsequently. Magnetic resonance imaging (MRI) pelvis was done which gave the possibility of paraganglioma. An excision of bladder mass was done and sent for histopathology. On histopathology accompanied by immunohistochemistry, a final diagnosis of paraganglioma was given. The patient is on regular follow-up.Entities:
Keywords: neuroendocrine; paraganglioma; primary; primary neuroendocrine tumor; rare case report; rare tumors; urinary bladder; urinary bladder tumor
Year: 2022 PMID: 35371661 PMCID: PMC8971093 DOI: 10.7759/cureus.22720
Source DB: PubMed Journal: Cureus ISSN: 2168-8184