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作 者:刘大看[1] 郭晓楠[1] 左松[1] 董长宪[1] Liu Dakan Guo Xiaonan Zuo Song Dong Changxian(Department of Hemangioma Surgery, Henan Provincial People's Hospital, Zhengzhou 450003, Chin)
出 处:《中华小儿外科杂志》2017年第1期25-27,共3页Chinese Journal of Pediatric Surgery
基 金:河南省卫生厅省部共建项目(2011010010)
摘 要:目的对Kasabach-Merritt综合征手术治疗过程中使用自体原位植皮术,评价其治疗效果,提出一种新的手术治疗方式。方法回顾性分析2010年至2015年间自体原位植皮手术治疗的Kasabach-Merritt综合征患儿23例,病例纳入标准:均为瘤体分布弥散,皮肤大面积(〉5cm×5cm)异常,手术切除瘤体后创面缝合困难;非手术治疗方法无效;血小板值在2×10^9/L^31×10^9/L。23例Kasabach-Merritt综合征患儿瘤体均位于四肢,上肢6例,下肢17例;男9例,女14例;年龄7d~9个月。总结该手术治疗方法的手术要点及术中、术后处理,分析治愈率及术后并发症。术后均经病理学检查证实为卡波西样血管内皮瘤(kaposiform hemangioendothelioma,KHE)20例,丛状血管瘤(tuftedangioma,TA)3例。结果23例患儿均在术后1周内血小板值恢复正常,随访1-5年,治愈率为100%;18例患儿自体皮片原位移植全部成活,有3例成活面积约90%,经后续换药处理后愈合,2例原位皮片移植成活约60%,行二期皮肤移植修补手术后治愈,术后并发症少。结论手术治疗Kasabach-Merritt综合征可作为有效的治疗方法,本组资料显示,自体原位植皮术作为一种新的手术方式,治愈率100%,术后并发症少,其对符合适应证者是一种可选择治疗手段。Objective To introduce one surgical approach for Kasabach-Merritt syndrome by autologous skin grafting and evaluated the effect of surgical treatment. Methods Retrospective analysis of autologous skin grafting was performed for 23 cases of Kasabach-Merritt syndrome. The area of tumor dispersion was 〉5 cm × 5 cm. Non-operative treatment was ineffective. Platelet count was under 2-31 × 10^9/L. All patients were confirmed postoperatively by pathological examination. The pathological diagnoses were KHE (kaposiform hernangioendothelioma, n = 20) and TA (tufted angioma, n = 3). Results All platelet counts recovered to normal within at 1 week post-operation. During a follow-up period of 1-5 years, the curative rate was 100%. And autologous skin grafts survived 100% (n = 18), 90%& healed after dressing (n=3) and 60% & healed after repairing (n= 2). Conclusions Autologous skin grafting is efficacious and has few complications for Kasabach- Merritt syndrome, especially tumor involvement of large skin area.
关 键 词:卡萨巴赫-梅里特综合征 皮肤移植术 全厚皮片
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