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尿素与甲基强的松龙联合介入治疗颌面部重症血管瘤伴血小板减少 被引量:7

Interventional therapy with urea and methylprednisolone in management of severe maxillofacial hemangioma with thrombocytopenia
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摘要 目的探讨婴幼儿颌面部重症血管瘤伴血小板减少的治疗方法。方法收集分析2001至2006年我科收治的35例颌面部重症血管瘤伴血小板减少患儿的临床表现及治疗经过,年龄最小10d,最大5个月,平均31d,血小板明显减低,在76×10^9/L以下,最低至6.2×10^9/L,采用颈外动脉结扎置管、40%尿素溶液与甲基强的松龙针剂联合介入治疗的方法。平均随访1年8个月。结果35例患儿中,血小板计数3~7d恢复到正常的30例,8~11d5例;血管瘤瘤体逐渐缩小,6~12个月消失28例,13~23个月7例。其中3例出现病情反复。结论颈外动脉结扎置管、尿素与甲基强的松龙联合介入治疗婴幼儿颌面部重症血管瘤伴血小板减少,疗效确切,创伤小,副作用少。本疗法操作简便,不需要特殊设备,易于推广,是一种较为理想的治疗小儿颌面部重症血管瘤伴血小板减少的方法。 Objective To evaluate the treatment of severe infantile maxillofaeial hemangioma associated with thrombocytopenia. Methods Thirty five cases of severe maxillofacial hemangioma with thrombocytopenia managed in our hospital between 2001 and 2006 were reviewed. The mean age was thirty one days, ranging from ten days to five months. The platelet count in these cases was below 76 ×10^9/L. The lowest platelete count was 6. 2 ×10^9/L. All the patients were treated with ligation of external carotid artery,insertion of a tube inside the lesion and injection of 40% urea and methylprednisolone. The average follow up period was one year and eight months. Results Among the 35 cases, the thrombocyte count in 30 cases returned to normal within 3-7 days. In the remaining 5 cases, it normalized within 8-11 days. The size of the hemangiomas decreased gradually after the therapy. The hemangiomas in 28 cases disappeared completely in 6 12 months and 7 cases disappeared in 13-23 months. In the course of the therapy, three cases were recurrent in these cases. Conclusions The urea combined with methylprednisolone interventional therapy is a reliable method with minimal side-effect and trauma. It requires no special instruments and is easy to popularize. It is a better method for the severe he mangioma of children in maxillofacial region.
出处 《中华小儿外科杂志》 CSCD 北大核心 2009年第1期17-19,共3页 Chinese Journal of Pediatric Surgery
基金 基金项目:河南省科技攻关项目(项目编号:0324410130)
关键词 血管瘤 血小板减少 尿素 Hemangioma Thrombocytopenia Urea
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  • 1Drolet BA, Esterly NB, Frieden IJ. Hemangiomas in children. N Engl J Med,1999,341 : 173-181.
  • 2Maguiness S, Guentber L. Kasabach-Merritt syndrome. J Cutan Med Surg, 2002,6 : 335-339.
  • 3Frevel T,Rabe H, Ckert F, et al. Giant cavernous haemangioma with Kasabach-Merritt syndrome : a case report and review. Eur J Pediatr, 2002,161 : 243-246.
  • 4MuIliken JB, Glowaeki J. Hemangiomas and vascular malformations in infants and children: a classification based on endothelial characteristics. Plast Reconstr Surg, 1982,69 : 412-420.
  • 5张连仲,董长宪,吴刚,赵冰,李桂芝.彩色多普勒超声鉴别小儿皮肤软组织血管瘤与血管畸形[J].中华超声影像学杂志,2000,9(8):475-476. 被引量:30
  • 6李晓瑜,余慕雪,陈东平,庄思齐,陈玮琪,刘美娜.新生儿Kasabach-Merritt综合征5例报道并文献复习[J].中国优生与遗传杂志,2006,14(6):87-88. 被引量:5
  • 7Larsen EC,Zinkham WH, Eggleston JC, et al. Kasabach - Merritt syndrome: therapeutic consideration. Pediatrics, 1987, 79: 971-980.
  • 8董长宪,马玉春,李恭才,张连仲,郭会斌.尿素介入治疗面颌部重症海绵状血管瘤[J].中华整形外科杂志,2004,20(4):316-317. 被引量:20
  • 9董长宪,马玉春,李振鲁,李恭才,郭会斌.尿素介入治疗面部毛细血管瘤[J].中华皮肤科杂志,2003,36(12):751-751. 被引量:6
  • 10Hesselmann S, Micke O, Marquardt T, et al. Case report: Kasabach-Merritt syndrome: a review of the therapeutic option and a case report of successful treatment with radiotherapy and interferon alphs, Br J Radiol, 2002,75: 180-184.

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