Ewing's sarcoma of the finger: Report of two cases and literature review

被引：7

作者：

Baccari, S. ^{[2
]}

Hamdi, M. F. ^{[1
]}

Mabrouki, Z. ^{[2
]}

Daghfous, M. ^{[2
]}

Tarhouni, L. ^{[2
]}

机构：

[1] Fattouma Bourguiba Univ Hosp, Dept Trauma & Orthopaed Surg, Monastir 5000, Tunisia

[2] Kassab Inst Traumat & Orthopaed Surg, Dept Hand & Reconstruct Surg, Manouba 2010, Tunisia

来源：

ORTHOPAEDICS & TRAUMATOLOGY-SURGERY & RESEARCH | 2012年 / 98卷 / 02期

关键词：

Chemotherapy; Ewing's sarcoma; Finger; Surgery; HAND; PHALANX; THUMB; BONE;

D O I：

10.1016/j.otsr.2011.06.012

中图分类号：

R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学（修复外科学）];

学科分类号：

摘要：

Ewing's sarcoma of the finger is extremely rare. Pain and swelling of the affected finger are the most frequent presenting features. We report two cases of Ewing's sarcoma located at ring finger and the thumb in two children aged 14 and 10 years. The first patient died of generalised metastases despite surgery, chemotherapy and radiation therapy. The second had no localised recurrence or metastases after surgery and chemotherapy at last follow-up of 4.5 years after tumour resection. The tumour's surgical accessibility, chemotherapy, and radiation therapy improve the prognosis of this tumour. (C) 2012 Elsevier Masson SAS. All rights reserved.

引用

页码：233 / 237

页数：5

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