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作 者:王冠男[1] 孙宁[1] 张潍平[1] 田军[1] 李明磊[1] 宋宏程[1] 杨洋[1] 林德富[1] Wang Guannan;Sun Ning;Zhang Weiping;Tian Jun;Li Minglei;Song Hongcheng;Yang Yang;Lin Defu(Department of Urology,Affiliated Beijing Children's Hospital,Capital Medical University,Beijing 100045,China)
机构地区:[1]首都医科大学附属北京儿童医院泌尿外科,100045
出 处:《中华小儿外科杂志》2018年第9期670-675,共6页Chinese Journal of Pediatric Surgery
基 金:北京市医院管理局"登峰"人才培养计划(DEL20151102); 北京市医院管理局"杨帆计划":小儿泌尿外科(ZYLX201709)
摘 要:目的 探讨儿童肾透明细胞肉瘤(clear cell sarcoma of the kidney,CCSK)的临床、病理特点及治疗.方法 回顾性分析2007年1月至2018年1月收治的20例CCSK患儿的临床及随访资料.其中,男11例,女9例;平均发病年龄32个月;左侧11例,右侧9例.临床表现为肉眼血尿6例,腹部包块10例,体检行腹部超声发现占位3例,腹痛1例.合并肾静脉瘤栓1例,合并腔静脉及右心房瘤栓1例.术前发现骨转移1例,肺转移并脑转移1例.结果 全部20例患儿均行瘤肾切除术,术后病理检查均提示为肾透明细胞肉瘤.按NWTS-5进行肿瘤分期:Ⅰ期11例,Ⅱ期1例,Ⅲ期6例,Ⅳ期2例.4例患儿接受术前长春新碱+放线菌素D化疗,19例患儿接受术后长春新碱、环磷酰胺、阿霉素、依托泊苷化疗+放疗.1例患儿因年龄小(3月龄)仅接受化疗、未接受放疗.20例患儿中,19例获访,随访时间1.5~123.0个月,平均56.1个月,存活最长的2例分别为108和85个月,6例死亡,1例失访.结论 儿童肾透明细胞肉瘤好发于3岁以下婴幼儿,易发生骨、脑转移,术前诊断困难,恶性度高、预后差,需采用手术+化疗+放疗的强化治疗.Objective To explore the clinicopathological features and treatment of clear cell sarcoma of kidney (CCSK)in children.Methods The clinical and follow-up data were retrospectively analyzed for 20 CCSK children admitted from January 2007 to January 2018 .There were 11 boys and 9 girls with an average age of 32 months.The involved sides were left (n=11)and right (n=9).The manifestations included gross hematuria (n=6),abdominal mass (n=10)and abdominal pain (n=1). Three cases were detected by abdominal examination.There were renal vein tumor thrombus (n=1 ), vena cava and right atrium tumor thrombus (n=1),preoperative bone metastases (n=1 )and lung &brain metastases (n=1).Results For 19 cases,the average follow-up period was 56.1 (1 .5-123.0) months.The longest two surviving cases were 108 and 85 months respectively.Six cases died and 1 case was follow-up.All of them underwent nephrectomy.Postoperative pathology indicated renal clear cell sarcoma.Performed according to NWTS-5,tumor stages were Ⅰ (n = 11 ),Ⅱ (n = 1 ),Ⅲ (n =6) and Ⅳ (n=2).Preoperative chemotherapy (n =4)and postoperative chemotherapy plus radiotherapy (n = 19)were offered.One patient received chemotherapy alone without radiotherapy because of its young age (3 months).Conclusions Clear cell sarcoma of kidney usually occur in infants aged under 3 years and are prone to bone and brain metastases.Preoperative diagnosis is difficult and there is high malignancy and poor prognosis.Intensive treatment of surgery plus chemotherapy plus radiotherapy is needed.
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