Bozbora Alp, Barbaros Umut, Erbil Yesim, Kiliçarslan Isin, Yildizhan Esra, Ozarmagan Selcuk
Department of General Surgery, Istanbul University, Istanbul Medical School, Capa, Istanbul, Turkey.
JSLS. 2006 Apr-Jun;10(2):263-6.
Bladder pheochromocytomas are extremely rare and constitute less than 5% of bladder tumors. The initial symptoms of the patient are mostly nonspecific caused by hypertension. The postmicturition hypertensive crisis is the typical warning sign of this disease. In this article, we present a 29-year-old female having hypertensive attacks following micturition. Radiological imaging techniques revealed a 3 x 3 x 4-cm bladder tumor that was hormonally active. This is the first case reported of bladder pheochromocytoma that was laparoscopically treated without using the adjunct transurethral resection. The postoperative follow-up of the patient confirms the success of the surgical procedure.
膀胱嗜铬细胞瘤极为罕见,占膀胱肿瘤的比例不到5%。患者的初始症状大多由高血压引起,缺乏特异性。排尿后高血压危象是该病的典型警示信号。在本文中,我们介绍了一名29岁的女性,她在排尿后出现高血压发作。放射影像学检查发现一个3×3×4厘米大小、具有激素活性的膀胱肿瘤。这是首例报道的经腹腔镜治疗且未辅助经尿道切除术的膀胱嗜铬细胞瘤病例。对该患者的术后随访证实了手术的成功。