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皮肤尤文肉瘤:2例报告及其他76例报告病例的临床表现、治疗及预后的文献综述

Cutaneous Ewing sarcoma: report of 2 cases and literature review of presentation, treatment, and outcome of 76 other reported cases.

作者信息

Collier Anderson B, Simpson Lesley, Monteleone Philip

机构信息

Department of Pediatrics, Lehigh Valley Hospital Health Network, University of South Florida College of Medicine, Bethlehem, PA, USA.

出版信息

J Pediatr Hematol Oncol. 2011 Dec;33(8):631-4. doi: 10.1097/MPH.0b013e31821b234d.

Abstract

Cutaneous Ewing sarcoma is a rare variant that has been poorly characterized and has no standard therapy. We report 2 patients with cutaneous Ewing sarcoma and review 76 other cases reported in the literature for demographics, presentation, treatment, and outcome. Only 2 patients presented with metastatic disease, and only 8 patients developed metastatic disease. Ninety-one percent of all patients are alive despite wide variations in treatment regimens. On the basis of this summary, treatment consisting of local control with surgery and/or radiation and abbreviated chemotherapy is proposed as a treatment option for this less aggressive Ewing sarcoma.

摘要

皮肤尤文肉瘤是一种罕见的变异型,其特征描述不足且尚无标准治疗方法。我们报告了2例皮肤尤文肉瘤患者,并回顾了文献中报道的其他76例病例的人口统计学、临床表现、治疗及预后情况。仅有2例患者就诊时即有转移性疾病,仅有8例患者出现转移性疾病。尽管治疗方案差异很大,但所有患者中有91%仍然存活。基于这一总结,对于这种侵袭性较低的尤文肉瘤,建议采用手术和/或放疗进行局部控制并联合短程化疗的治疗方案。

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