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首页> 外文期刊>International journal of surgical pathology >Giant Cell Tumor of Bone With Pseudosarcomatous Changes Leading to Premature Denosumab Therapy Interruption: A Case Report With Review of the Literature
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Giant Cell Tumor of Bone With Pseudosarcomatous Changes Leading to Premature Denosumab Therapy Interruption: A Case Report With Review of the Literature

机译:假性肉瘤样改变导致过早的Denosumab治疗中断的骨巨细胞瘤:一例报道并文献复习

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摘要

Denosumab has shown promising results in the management of giant cell tumor of bone, a primary bone tumor with locally aggressive behaviour. We report a case of premature denosumab interruption due to radiological and clinical tumor expansion of a giant cell tumor of the distal ulna. Although denosumab is known to induce tumor regression, with progressive ossification and loss of the characteristic morphology of giant cell tumor of bone, the ulnar tumor specimen showed a moderately to highly cellular proliferation of short spindle-shaped cells, and no osteoclast-like giant cells. There were no abnormal mitotic figures. We considered the surgical specimen as a giant cell tumor of bone with partial regression after prematurely interrupted denosumab treatment. This case illustrates the diagnostic issues of an initially unfavourable evolution raising concern for malignancy, and the difficulties in histological assessment of a partially treated giant cell tumor of bone, that may mimic osteosarcoma.
机译:地诺单抗在骨巨细胞瘤的治疗中显示出令人鼓舞的结果,骨巨细胞瘤是具有局部侵袭性的原发性骨肿瘤。我们报道了由于尺骨远端巨细胞瘤的放射学和临床肿瘤扩张而导致地诺单抗过早中断的情况。尽管已知狄诺塞麦可诱导肿瘤消退,但随着骨化的进行以及骨巨细胞瘤特征性形态的丧失,尺骨肿瘤标本显示短梭形细胞呈中等至高度细胞增殖,无破骨细胞样巨细胞。没有异常的有丝分裂图。我们认为手术标本是在诺美单抗治疗过早中断后部分消退的骨巨细胞瘤。该病例说明了最初不利发展的诊断问题,引起了对恶性肿瘤的关注,以及对部分治疗的骨巨细胞瘤(可能模仿骨肉瘤)进行组织学评估的困难。

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