Brotzmann M, Hefti F, Baumhoer D, Krieg A H
Orthopaedic Department, Basel University Childrens Hospital (UKBB), Spitalstrasse 33, 4056 Basel, Switzerland.
Sarcoma. 2013;2013:767960. doi: 10.1155/2013/767960. Epub 2013 Mar 20.
We analyze the delay in diagnosis and tumor size of malignant bone tumors of the foot in a retrospective study. We compared the oncological and surgical long-term results with identical tumor at other anatomical sites in order to analyze the biological behavior of sarcomas that are found in the foot. Thirty-two patients with a histologically proven malignant bone tumor (fifteen chondrosarcomas, nine osteosarcomas, and eight Ewing sarcomas) between the years 1969 and 2008 were included. The median follow-up was 11.9 years. The overall median time gap between the beginning of symptoms and diagnosis in the study group was 10 months. Ewing sarcoma presented with the longest delay in diagnosis (median of 18 months), followed by osteosarcoma (median of 15 months) and chondrosarcoma (median of 7.5 months). The delay in diagnosis of these tumors was significantly longer than that of equivalent tumors at other skeletal sites, but the 5- and 10-year survival rates and the occurrence of distant metastases were comparable. In contrast, the average size of foot tumors was 5- to 30-fold less than that of tumors analyzed at other skeletal sites. This study indicates that sarcomas of the foot demonstrate a distinct biological behavior compared to the same tumor types at other skeletal sites.
我们通过一项回顾性研究分析了足部恶性骨肿瘤的诊断延迟情况和肿瘤大小。我们将足部肿瘤的肿瘤学及手术长期结果与其他解剖部位相同肿瘤的结果进行比较,以分析足部肉瘤的生物学行为。研究纳入了1969年至2008年间32例经组织学证实的恶性骨肿瘤患者(15例软骨肉瘤、9例骨肉瘤和8例尤因肉瘤)。中位随访时间为11.9年。研究组症状开始至诊断的总体中位时间间隔为10个月。尤因肉瘤的诊断延迟最长(中位18个月),其次是骨肉瘤(中位15个月)和软骨肉瘤(中位7.5个月)。这些肿瘤的诊断延迟明显长于其他骨骼部位同等肿瘤,但5年和10年生存率以及远处转移的发生率相当。相比之下,足部肿瘤的平均大小比其他骨骼部位分析的肿瘤小5至30倍。这项研究表明,与其他骨骼部位相同肿瘤类型相比,足部肉瘤表现出独特的生物学行为。