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Primary giant cell tumor of soft tissues similar to bone giant cell tumor: A case report and literature review.

机译:与骨巨细胞瘤相似的软组织原发性巨细胞瘤:1例报道并文献复习。

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摘要

In this report we describe a primary giant cell tumor (GCT) of soft tissues located in the left dorsal wrist of a 52-year-old man. Plain radiographs did not reveal any lesion in his carpal or hand bones. Although the tumor was clinically considered a ganglion initially, the microscopic features were identical to those found in classic GCT of bone. Light microscopy showed a lesion composed of a homogeneously mixed proliferation of spindle and polygonal mononucleated stromal cells and evenly distributed multinucleated, osteoclast-like giant cells. Whereas most bone tumors have an extraosseous counterpart, only 13 cases of GCT in soft tissues had been published until 1998. Moreover, 64 new cases have been reported in three series. Nevertheless, most major reviews and textbooks do not consider this tumor as a specific entity and regard it as a low grade variant of malignant GCT of soft tissue. We describe the clinical, histologic, and immunohistochemical features of this rare benign neoplasm emphasizing the differential diagnosis with its malignant soft tissue counterpart, an ominous tumor.
机译:在本报告中,我们描述了位于52岁男性左手腕的软组织原发性巨细胞瘤(GCT)。普通的X光片未显示出他的腕骨或手骨有任何病变。尽管最初在临床上将肿瘤视为神经节,但其微观特征与经典的GCT骨骼相同。光学显微镜显示病变由梭形和多边形单核基质细胞的均匀混合增殖以及均匀分布的多核破骨细胞样巨细胞组成。尽管大多数骨肿瘤都具有骨外对应物,但直到1998年,软组织中仅发生了13例GCT病例。此外,三个系列报道了64例新病例。然而,大多数主要的评论和教科书并未将这种肿瘤视为特定实体,而是将其视为软组织恶性GCT的低度变异。我们描述了这种罕见的良性肿瘤的临床,组织学和免疫组化特征,强调了其恶性软组织对应物(不祥肿瘤)的鉴别诊断。

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