Case Report

Vol. 26 No. 2 (2022): Endocrinology Research and Practice

A Giant Urinary Bladder Paraganglioma

Main Article Content

Raiz Ahmad Misgar
Mohammad Salem Baba
Abid Hussain Bhat
Abdul Rouf Khawaja
Mohammad Iqbal Lone
Mir Iftikhar Bashir
Arshad Iqbal Wani

Abstract

Paragangliomas are catecholamine-secreting neuroendocrine tumors originating from extra- adrenal neural crest cells. Urinary bladder paragangliomas are extremely rare and usually present with micturition-related hypertension, palpitations, headaches, dizziness, and sweating. We report a middle-aged female with a giant urinary bladder paraganglioma that was symptomatic for 6 years but unfortunately remained undiagnosed for more than half a decade. The patient exhibited the typi- cal noradrenergic biochemical phenotype that characterizes paragangliomas. The patient was suc- cessfully managed with subtotal cystectomy and augmentation cystoplasty. Ours is the patient with largest reported case of urinary bladder paraganglioma and the only one managed with augmenta- tion cystoplasty.



Cite this article as: Misgar RA, Baba MS, Bhat AH, et al. A giant urinary bladder paraganglioma. Turk J Endocrinol Metab. 2022;26(2):100-102.



 


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