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Soft Tissue Giant Cell Tumor of Low Malignant Potential of Mediastinum: A Rare Case Report

机译:低纵隔恶性肿瘤的软组织巨细胞瘤:罕见病例报告

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摘要

Giant cell tumor (GCT) is primarily a bone neoplasm. Rare origin of the tumor from soft tissues has been reported. Involvement of mediastinum by GCT is even rarer. We herein describe an interesting case of huge mediastinal tumor in a young man. Radiologically, no primary osseous lesion was present throughout the body. Morphologically, tumor resembles osseous GCT with increased mitotic activity. Hence, the case was diagnosed as soft tissue GCT of low malignant potential at the rare site of mediastinum. To the best of our knowledge, the present case is the fourth reported case. Pathologists and clinicians need to be aware of the rare diagnosis of GCT in mediastinum and should carefully evaluate the clinical and radiological findings.
机译:巨细胞瘤(GCT)主要是骨肿瘤。据报道,肿瘤很少来自软组织。 GCT介入纵隔的情况更为罕见。我们在此描述了一个年轻人中巨大的纵隔肿瘤的有趣病例。放射学上,全身没有原发性骨病变。在形态上,肿瘤类似于骨GCT,但有丝分裂活性增加。因此,该病例被诊断为在纵隔罕见部位恶性潜能低的软组织GCT。据我们所知,本案是第四例。病理学家和临床医生需要意识到纵隔中GCT的罕见诊断,并应仔细评估临床和放射学发现。

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