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病例报告628:低级别中央型骨肉瘤。

Case report 628: Low-grade central osteosarcoma.

作者信息

Sim F H, Kurt A M, McLeod R A, Unni K K

机构信息

Department of Orthopedics, Mayo Clinic, Rochester, MN 55905.

出版信息

Skeletal Radiol. 1990;19(6):457-60. doi: 10.1007/BF00241806.

Abstract

In summary, low-grade central osteosarcoma is a clinically recognizable rare subtype of osteosarcoma, representing 1.9% of all osteosarcomas found at the Mayo Clinic. The lesion is locally aggressive but also has the potential for metastasis, particularly after local recurrence. The tumor may be difficult to distinguish radiographically and histologically from benign conditions, particularly fibrous dysplasia. This difficulty has led to inadequate treatment. In most cases, a wide surgical margin achieved by either local resection or amputation should result in a cure. Because of the low metastatic potential of the initial lesion, there seems to be no need for adjuvant chemotherapy.

摘要

总之,低级别中央型骨肉瘤是一种临床上可识别的罕见骨肉瘤亚型,占梅奥诊所发现的所有骨肉瘤的1.9%。该病变具有局部侵袭性,但也有转移的可能,尤其是在局部复发后。在影像学和组织学上,该肿瘤可能难以与良性病变区分开来,尤其是骨纤维异常增殖症。这种困难导致了治疗不足。在大多数情况下,通过局部切除或截肢实现的广泛手术切缘应能治愈。由于初始病变的转移潜力较低,似乎无需辅助化疗。

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