Patterson J W, Maygarden S J
J Cutan Pathol. 1986 Feb;13(1):46-58. doi: 10.1111/j.1600-0560.1986.tb00460.x.
We report the case of a 13-year-old girl with extraskeletal Ewing's sarcoma involving the skin and subcutaneous tissue of the upper back. The patient underwent wide local excision and right axillary node dissection, and received chemotherapy with vincristine, actinomycin D, and cyclophosphamide. There was no evidence of recurrence or metastasis in eight months of follow up. Light and electron microscopic features were typical for this neoplasm. Tumor cells contained abundant glycogen, but failed to stain for desmin, keratin, neuron-specific enolase, or S-100 protein. We discuss the differential diagnosis of extraskeletal Ewing's sarcoma as well as theories of its histogenesis.
我们报告了一例13岁女孩,其发生于背部上方皮肤及皮下组织的骨外尤因肉瘤。该患者接受了广泛局部切除及右腋窝淋巴结清扫术,并接受了长春新碱、放线菌素D和环磷酰胺化疗。随访8个月未见复发或转移迹象。光镜和电镜特征为此肿瘤所特有。肿瘤细胞含有丰富糖原,但结蛋白、角蛋白、神经元特异性烯醇化酶或S-100蛋白染色均为阴性。我们讨论了骨外尤因肉瘤的鉴别诊断及其组织发生学理论。