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青年(18~40岁)非透明细胞型肾恶性肿瘤患者的临床病理特点及预后

Clinicopathological features and prognosis of non-clear cell renal cell carcinoma in young patients aged 18-40 years

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【作者】 唐世英薛子璇董靖晗邱敏田晓军陆敏张树栋马潞林

【Author】 TANG Shiying;XUE Zixuan;DONG Jinghan;QIU Min;TIAN Xiaojun;LU Min;ZHANG Shudong;MA Lulin;Department of Urology,Peking University Third Hospital;Department of Pathology,Peking University Third Hospital;

【通讯作者】 邱敏;

【机构】 北京大学第三医院泌尿外科北京大学第三医院病理科

【摘要】 目的 分析总结单中心青年(18~40岁)非透明细胞型肾恶性肿瘤手术患者的临床、病理特征及预后,为同类患者的诊治提供参考。方法 回顾性分析2012年1月—2022年8月于北京大学第三医院泌尿外科收治的113例青年非透明细胞型肾恶性肿瘤手术患者的病例资料,其中男性57例(50.4%),女性56例(49.6%);平均发病年龄(31.6±5.8)岁;左侧57例(50.4%)、右侧56例(49.6%)。青年肾恶性肿瘤手术患者约占同期所有年龄段肾恶性肿瘤手术患者总数的12.4%,其中青年非透明细胞型肾恶性肿瘤手术患者占同期青年肾恶性肿瘤手术患者总数的34.8%。结果 102例(90.3%)患者行微创手术(腹腔镜或机器人辅助),另外11例(9.7%)行开放手术;肾部分切除术55例(48.7%),根治性肾切除术58例(51.3%),肾癌瘤栓患者11例(9.7%)。手术均顺利完成,围手术期无严重并发症发生。病理类型包括肾嫌色细胞癌32例(28.3%)、MiT家族易位性肾细胞癌25例(22.1%)、乳头状肾细胞癌20例(17.7%)、3种病理亚型合计占总体的68.1%。术后随访46(2~115)个月,8例(7.8%,8/102)出现肿瘤转移,2例死亡。结论 青年非透明细胞型肾恶性肿瘤相对少见,病理类型以嫌色细胞癌为主,微创手术仍是该类肾恶性肿瘤患者的主要治疗方式,多数病理类型远期预后较好,合并瘤栓患者转移风险高、预后较差。

【Abstract】 Objective To summarize the clinicopathological features and prognosis of young patients(18-40 years old) with non-clear cell renal cell carcinoma(nccRCC) treated in a single center to provide reference for the diagnosis and treatment of similar patients.Methods Clinical data of 113 nccRCC patients treated during Jan. 2012 and Aug. 2022 were retrospectively analyzed, including 57 males(50.4%) and 56 females(49.6%). The average age of onset was(31.6±5.8)years. Among all patients, 57 had lesions(50.4%) on the left side, and 56(49.6%) on the right side. Young patients undergoing renal cancer surgery accounted for approximately 12.4% of the total number of renal cancer patients undergoing surgery, and nccRCC accounted for 34.8% of the total number of cases. Results Minimally invasive surgery(laparoscopic or robot-assisted) was performed in 102 cases(90.3%), and open surgery in 11 cases(9.7%). Fifty-five cases(48.7%) underwent partial nephrectomy and 58(51.3%) radical nephrectomy. Among them, 11 patients(9.7%) developed tumor thrombi. All surgeries were successful with no serious complications. The pathological types included 32 cases(28.3%) of chromophobe renal cell carcinoma, 25 cases(22.1%) of MiT family translocation renal cell carcinoma, and 20 cases(17.7%) of papillary renal cell carcinoma. The total proportion of the three pathological subtypes reached 68.1%. After 46(2-115) months of follow-up, 8 cases(7.8%,8/102) developed tumor metastasis and 2 died.Conclusion The nccRCC is rare in young patients. The major pathological type is chromophobe, and the major treatment method is minimally invasive surgery. Most pathological types have good long-term prognosis, while patients with tumor thrombi have a high risk of metastasis and poor prognosis.

  • 【文献出处】 现代泌尿外科杂志 ,Journal of Modern Urology , 编辑部邮箱 ,2024年01期
  • 【分类号】R737.11
  • 【下载频次】28
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