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青少年骨原发性多形性脂肪肉瘤:一种罕见实体的影像学特征。

Primary pleomorphic liposarcoma of bone in an adolescent: imaging features of a rare entity.

机构信息

Department of Imaging and Interventional Radiology, Prince of Wales Hospital, Ngan Shing St, Shatin, New Territories, Hong Kong.

出版信息

Pediatr Radiol. 2011 Oct;41(10):1342-5. doi: 10.1007/s00247-011-2078-3. Epub 2011 May 15.

Abstract

We report a rare case of a primary osseous pleomorphic liposarcoma of the distal femur in a 13-year-old boy. Primary liposarcoma of bone is a very rare malignant tumour originating from primitive mesenchymal cells rather than mature adipose tissue. Pleomorphic liposarcoma is the least common of the eight known histological subtypes in the WHO classification. The entity is not previously reported in children. This is the third reported case of pleomorphic liposarcoma of the bone, and the first reported case presenting in adolescence. We describe the computed tomography and magnetic resonance imaging features of this rare bony tumour.

摘要

我们报告了一例罕见的 13 岁男孩股骨远端原发性骨多形性脂肪肉瘤。原发性骨脂肪肉瘤是一种非常罕见的恶性肿瘤,起源于原始间充质细胞,而不是成熟脂肪组织。多形性脂肪肉瘤是世界卫生组织分类中已知的 8 种组织学亚型中最不常见的一种。这种病变以前在儿童中没有报道过。这是第三例报告的骨多形性脂肪肉瘤病例,也是首例报告发生于青春期的病例。我们描述了这种罕见骨肿瘤的计算机断层扫描和磁共振成像特征。

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