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Soft tissue giant cell tumor of low malignant potential

机译:低恶性软组织巨细胞瘤

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Giant cell tumor of soft tissue (GCT-ST) is a rare tumor first described in 1972 by Salm and Sissons, followed shortly by Guccion and Enzinger. This tumor has been considered to be synonymous with the giant cell variant of malignant sarcoma with frequent local recurrence and metastasis. Recently GCT-ST has been described as a distinct entity of relatively benign prognosis, yet lacking marked atypia and pleomorphism, even in the presence of mitotic activity and vascular invasion. Now some authors think that GCT-ST represents the soft tissue analog of giant cell tumor of bone because of their histological and immunohistochemical similarity. Some reports documented these pathological new findings, but clinical case reports with description of imagings and surgery on the basis of these knowledge are very few. The authors describe the clinical, radiological, morphologic and histopathologial features of a case of GCT-ST occurring primarily in the subcutaneous tissue of the thigh with a review of the literature.
机译:软组织巨细胞瘤(GCT-ST)是一种罕见的肿瘤,于1972年由Salm和Sissons首次提出,随后由Guccion和Enzinger提出。该肿瘤被认为是恶性肉瘤的巨细胞变体,具有频繁的局部复发和转移。最近,GCT-ST被描述为相对良性预后的独特个体,即使在有丝分裂活动和血管浸润的情况下,也缺乏明显的非典型性和多态性。现在一些作者认为,由于GCT-ST的组织学和免疫组织化学相似性,它们代表了骨巨细胞瘤的软组织类似物。一些报告记录了这些病理学新发现,但是很少有基于这些知识的影像学和手术描述的临床病例报告。作者描述了主要发生在大腿皮下组织中的GCT-ST病例的临床,影像学,形态学和组织病理学特征,并进行了文献综述。

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