Reinus W R, Gilula L A, Shirley S K, Askin F B, Siegal G P
AJR Am J Roentgenol. 1985 Feb;144(2):331-6. doi: 10.2214/ajr.144.2.331.
Review of current data from the Intergroup Ewing Sarcoma Study (IESS) shows that Ewing sarcoma is rare in bones of the hands and feet. The 12 patients from the IESS protocols with hand or foot Ewing sarcoma are comparable to those already reported in the literature. With the exception of lesions in the calcaneus, the prognosis for disease-free survival is excellent. The radiographic features of hand and foot Ewing sarcoma are generally those of classic Ewing sarcoma: permeation, soft-tissue mass, and, often, associated sclerotic reaction. However, with the exception of sclerosis, features suggesting bone reaction and slow tumor growth in these patients were distinctly uncommon compared with Ewing sarcoma in general. Those radiographic features suggesting aggressive behavior were slightly more common than in the general Ewing population. Even so, neither the radiographic appearance nor the greatest dimension of the radiographic lesion can be shown to contribute significantly to prognostication in these patients. Apparently location of the lesion is important, since in the reported cases in the literature and in this series, lesions of the calcaneus fared poorly. The importance of this set of patients therefore relates to awareness and early recognition of an unusual appearance and location of Ewing sarcoma.
对尤因肉瘤协作组研究(IESS)的当前数据进行回顾显示,尤因肉瘤在手和足部骨骼中较为罕见。IESS方案中的12例手或足部尤因肉瘤患者与文献中已报道的患者情况相当。除跟骨病变外,无病生存预后良好。手和足部尤因肉瘤的影像学特征通常是典型尤因肉瘤的特征:骨质浸润、软组织肿块,且常伴有硬化反应。然而,除硬化外,与一般尤因肉瘤相比,这些患者中提示骨反应和肿瘤生长缓慢的特征明显少见。那些提示侵袭性行为的影像学特征比一般尤因肉瘤患者群体略为常见。即便如此,影像学表现或影像学病变的最大尺寸均未显示对这些患者的预后有显著影响。显然病变部位很重要,因为在文献报道的病例以及本系列病例中,跟骨病变预后较差。因此,这类患者的重要性在于提高对尤因肉瘤不寻常表现和部位的认识并尽早识别。