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作 者:孙明[1] 刘学锋[1] 潘春雨[1] 张峰[1] 赵文嫣[2] 吴斌[1]
机构地区:[1]中国医科大学附属盛京医院泌尿外科,辽宁沈阳110004 [2]中国医科大学附属盛京医院普通外科,辽宁沈阳110004
出 处:《现代肿瘤医学》2016年第9期1417-1420,共4页Journal of Modern Oncology
摘 要:目的:探讨肾嫌色细胞癌(renal chromophobe cell carcinoma,RCCC)的临床特征、病理学特点、诊断、治疗方法和预后。方法:回顾性分析2010年2月至2015年4月期间经病理检查证实的11例RCCC患者的临床资料,结合相关文献复习并进行讨论。结果:11例患者中7例男性,4例女性,年龄40~71岁,平均59岁。肿物直径3.5~14.5cm。病变位于右侧者6例,左侧5例。术前无症状者6例,单纯性腰背部疼痛不适5例。11例患者均经CT检查确诊,均行手术治疗。手术过程顺利,术后均有病理证实为肾嫌色细胞癌。出院后随访3~36个月,无肿瘤复发和转移。结论:RCCC是一种低度恶性,少见的肾脏肿瘤。手术治疗是首选方法,预后较好。Objective: To investigate the clinical features, pathological characteristics, diagnosis, treatment and prognosis of renal chromophobe cell carcinoma(RCCC). Methods:Clinical data of 11 cases of RCCC were analyzed retrospectively and pertinent literatures were reviewed. Results:Seven cases were males and 4 cases were females, aged 40 -71, averaged 59 years old. Bump diameter 3.5 - 14.5cm. 6 cases were on the right kidney and the other cases were on the left side. 6 cases had no symptoms,5 cases complained about simple backache. 11 cases were all taken CT scan for diagnosis and undertaken open or laparoscopic surgery. During 3 to 36 months follow -up, no tumor relapse. Conclusion :RCCC is a low grade rare renal tumor and the treatment mainly depends on the surgery. Surgery was the preferred method of treatment, and the prognosis is good.
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