Seki N, Mukai S, Gamachi A, Migita T, Maeda K, Ogata N
Department of Urology, Oita Prefectural Hospital, Oita, Japan.
Urol Int. 2001;66(1):57-60. doi: 10.1159/000056569.
The clinical picture of bladder pheochromocytoma is usually typical; however, the diagnosis is occasionally delayed because of the rarity of this neoplasm. We report a case of unsuspected bladder pheochromocytoma in which the patient had a hypertensive episode during transurethral resection. A 67-year-old male presented with the chief complaint of painless macrohematuria. Cystoscopy revealed a submucosal tumor on the right lateral wall of the bladder. The tumor was operated on transurethrally, followed by partial cystectomy. The pathological diagnosis was pheochromocytoma, primarily occurring in the bladder. Treatment of this lesion requires a high degree of clinical suspicion based on the patient's symptom complex in order to enable adequate preparation prior to surgical manipulation.
膀胱嗜铬细胞瘤的临床表现通常较为典型;然而,由于这种肿瘤罕见,诊断偶尔会延迟。我们报告一例未被怀疑的膀胱嗜铬细胞瘤病例,该患者在经尿道切除术中出现高血压发作。一名67岁男性以无痛性肉眼血尿为主诉就诊。膀胱镜检查发现膀胱右侧壁有一个黏膜下肿瘤。该肿瘤经尿道手术切除,随后行膀胱部分切除术。病理诊断为嗜铬细胞瘤,主要发生于膀胱。对于该病变的治疗,需要根据患者的症状综合表现进行高度的临床怀疑,以便在手术操作前做好充分准备。