Shirley S K, Askin F B, Gilula L A, Vietti T J, Thomas P R, Siegal G P, Reinus W R, Kissane J M, Nesbit M E
J Clin Oncol. 1985 May;3(5):686-97. doi: 10.1200/JCO.1985.3.5.686.
Review of current data from the Intergroup Ewing's Sarcoma Study (IESS) shows that Ewing's sarcoma (ES) is rare in bones of the hands and feet. Only 12 of 377 evaluable patients in the first two IESS studies had a primary tumor in these small, distal bones. The age distribution was typical for that seen in patients with ES at other sites. Males were affected twice as often as females, and tumors in the bones of the feet were much more common than those in the hands. All signs and symptoms were local in distribution. As in other sites, the dominant histologic pattern was categorized as diffuse. With the exception of those patients with lesions in the calcaneus, the prognosis for disease-free survival was excellent. A literature review of cases of ES reported in bones of the hands and feet showed generally comparable results.
对国际尤因肉瘤研究组(IESS)当前数据的回顾显示,尤因肉瘤(ES)在手和足部骨骼中较为罕见。在前两项IESS研究的377例可评估患者中,只有12例在这些小的远端骨骼中有原发性肿瘤。年龄分布与其他部位ES患者所见典型。男性受影响的频率是女性的两倍,足部骨骼中的肿瘤比手部的更为常见。所有体征和症状均呈局部分布。与其他部位一样,主要组织学模式被归类为弥漫性。除跟骨有病变的患者外,无病生存预后良好。对手和足部骨骼中报道的ES病例进行的文献综述显示结果总体相当。