Gyftopoulos K, Perimenis P, Ravazoula P, Athanassopoulos A, Barbalias G A
Department of Urology, University Hospital Patras, Patras, Greece.
Urol Int. 2000;65(3):173-5. doi: 10.1159/000064867.
Pheochromocytoma of the bladder is an unusual tumor that typically presents with hypertensive crises related to micturition. We describe a case of bladder pheochromocytoma in a 42-year-old female in which macroscopic hematuria was the only alarming symptom. The diagnostic and operative issues of this type of tumor are discussed, along with the challenging treatment option of transurethral resection. Diagnosis, treatment and follow-up trends of this rare tumor are reviewed.
膀胱嗜铬细胞瘤是一种罕见的肿瘤,通常表现为与排尿相关的高血压危象。我们描述了一例42岁女性膀胱嗜铬细胞瘤病例,其中肉眼血尿是唯一令人担忧的症状。本文讨论了这类肿瘤的诊断和手术问题,以及经尿道切除术这一具有挑战性的治疗选择。同时对这种罕见肿瘤的诊断、治疗及随访趋势进行了综述。