Freilinger G, Konrad K
Plast Reconstr Surg. 1984 Mar;73(3):462-5. doi: 10.1097/00006534-198403000-00025.
The first appearance, the 12-year follow-up, and the autopsy of a patient with a strange soft-tissue tumor in the lower leg region are described. Although it was originally taken for a malignant synovial tumor, its peculiar distribution pattern, together with its histologic picture, confirmed the final diagnosis as an epithelioid sarcoma.
本文描述了一名小腿部患有罕见软组织肿瘤患者的首次发病情况、12年随访过程以及尸检结果。尽管最初被误诊为恶性滑膜肿瘤，但因其特殊的分布模式以及组织学表现，最终确诊为上皮样肉瘤。
