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Giant cell tumor of soft tissues of low malignant potential: A rare diagnosis on fine needle aspiration cytology

机译:低恶性软组织巨细胞瘤:细针穿刺细胞学检查的罕见诊断

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Primary giant cell tumors of soft tissues (GCT-ST) are extremely rare soft tissue tumors, located in both superficial and deep soft tissues. They resemble osseous giant cell tumors morphologically and immunohistochemically. The tumor exhibits strong positive immunoreactivity for cluster of differentiation 68 (CD68) within multinucleated osteoclast-like giant cells and focal staining of mononuclear cells. Case reports describing the cytohistological features of this entity are very few. We report a case of GCT-ST of low malignant potential diagnosed on fine needle aspiration (FNA) and confirmed on histological and immunohistochemical studies.
机译:软组织的原发性巨细胞瘤(GCT-ST)是极为罕见的软组织肿瘤,位于浅表和深部软组织中。它们在形态和免疫组织化学上均类似于骨性巨细胞瘤。肿瘤对多核破骨细胞样巨细胞内的分化簇68(CD68)和单核细胞的局部染色表现出强阳性免疫反应性。描述该实体的细胞组织学特征的病例报告很少。我们报告一例通过细针穿刺(FNA)诊断出的低恶性潜能的GCT-ST病例,并在组织学和免疫组织化学研究中得到证实。

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