Mastering bladder paraganglioma for optimal treatment: a case report of robot-assisted surgery

Author:

Orsini Angelo1ORCID,Ferretti Simone2,Tamborino Flavia2,Cicchetti Rossella2,Ciavarella Davide2,Seccia Barbara3,Basilico Raffaella4,Colasante Antonella5,Marchioni Michele6,Schips Luigi2

Affiliation:

1. Department of Urology, SS Annunziata Hospital, ‘G. D’Annunzio’ University of Chieti, Via dei Vestini, Chieti, Italy

2. Department of Medical, Oral and Biotechnological Sciences, ‘G. d’Annunzio’ University of Chieti, Urology Unit, Chieti, Italy

3. Department of Neuroscience, Imaging and Clinical Sciences, ‘G. d’Annunzio’ University of Chieti, Chieti, Italy

4. Department of Medical, Oral and Biotechnological Sciences, ‘G. d’Annunzio’ University of Chieti, Radiology Unit, Chieti, Italy

5. Department of Surgical Pathology, SS Annunziata Hospital, Chieti, Italy

6. Department of Urology, SS Annunziata Hospital, ‘G. D’Annunzio’ University of Chieti, Via dei Vestini, Chieti 66100, Italy

Abstract

Bladder paraganglioma is a rare neuroendocrine neoplasm, either functional or non-functional, arising from the urinary bladder. Functional variants present with catecholamine-related symptoms, while non-functional variants pose diagnostic challenges, mimicking urothelial carcinoma. Misdiagnosis risks underscore the importance of accurate identification for appropriate patient management. In this case, a 52-year-old man, diagnosed incidentally with hypertension and reported occasional post-micturition tachycardia, underwent abdominal ultrasound for known hepatic cyst follow-up, revealing an oval hypoechoic bladder mass. Initial consideration of bladder urothelial carcinoma prompted further investigation with contrast-enhanced CT scan and cystoscopy that confirmed extrinsic mass nature, and subsequent robotic-assisted partial cystectomy was performed. Histologically, the removed mass exhibited characteristic features of bladder paraganglioma. Postoperative recovery was uneventful, with resolution of post-micturition tachycardia at 1 month. Follow-up includes endocrinological evaluation and a 6-month CT scan. In conclusion, bladder paraganglioma should be considered in para-vesical mass differentials. This case highlights the importance of meticulous history collection, even in asymptomatic patients, the need for a multidisciplinary approach for accurate diagnosis and management of this rare condition, and the robotic approach as a viable option.

Publisher

SAGE Publications

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