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作 者:Fariba Binesh Kazem Aghili Jalil Zare Yavar Rajabzadeh
机构地区:[1]Department of Pathology, Shahid Sadoughi University of Medical Sciences [2]Department of Radiology, Shahid Sadoughi University of Medical Sciences [3]Orthopaedic Surgery, Shahid Sadoughi University of Medical Sciences
出 处:《The Chinese-German Journal of Clinical Oncology》2012年第10期612-614,共3页中德临床肿瘤学杂志(英文版)
基 金:Supported by Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, Iran
摘 要:Giant cell tumor (GCT) of the bone is a benign but locally aggressive & destructive lesion. This tumor is usually seen in patients over 20 years of age. Less than 2% are found in part with open epiphysis. The epiphyseal portion of the bone is characteristic site of giant cell tumor. In rare instances, giant cell tumor can occur in the diaphysis of long tubular bone without involving the epiphysis. Although age, clinical and radiological features are helpful, it is still the histology that helps to clinch the diagnosis. It is important to distinguish giant cell tumor of diaphysis from the giant cell rich lesions, more common in this site.
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