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An unusual tumor of rib diaphysis—report of a giant cell tumor and a brief review of literature

机译:肋骨骨干异常的肿瘤-报告巨细胞瘤并简要回顾了文献

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摘要

Giant Cell Tumor of bone (GCT) is a benign but aggressive tumor, which forms about 4–5% of primary bone tumors and 1–2% of all chest wall tumors. It arises in the epiphysis of bones. The epiphysis of a rib is in its head and tubercle posteriorly and hence a GCT arising in a rib’s anterior aspect, its diaphysis, is rare. In this unusual position, it can be mistaken for other more common diaphyseal pathologies. Radiological images are often diagnostic. A needle biopsy is best avoided and a wide excision biopsy is the treatment of choice. Microscopically, multinucleated giant cells are seen amidst stromal cells. Giant cells like these are also seen in other diseases like the brown tumor of primary hyperparathyroidism. Giant cell lesions are never caused by secondary hyperparathyroidism. We present a case of a diaphyseal GCT of rib in a patient with secondary hyperparathyroidism who was successfully treated.
机译:骨巨细胞瘤(GCT)是一种良性但具有侵略性的肿瘤,约占原发性骨肿瘤的4–5%和所有胸壁肿瘤的1-2%。它出现在骨骼的骨physi中。肋骨的骨physi位于其头部和结节的后方,因此很少出现在肋骨的前侧产生的GCT,即骨干。在这种不寻常的位置,它可能会被误认为其他更常见的干病。放射图像通常是诊断性的。最好避免进行穿刺活检,选择广泛的活检是一种治疗方法。显微镜下可见间质细胞中有多核巨细胞。在其他疾病中,例如原发性甲状旁腺功能亢进症的棕色肿瘤中,也可以看到这种巨细胞。巨细胞病变绝不是由继发性甲状旁腺功能亢进引起的。我们介绍了一例成功治疗的继发性甲状旁腺功能亢进患者肋骨干G端CT。

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