间充质软骨肉瘤:一种罕见的侵袭性软骨肉瘤

A. Jhunjhunwala, Arnab Ghosh, M. Shrestha, Dilasma Ghartimagar, S. Thapa, S. Regmi, B. Dhakal
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引用次数: 0

摘要

一个15岁的男孩报告了2个月的严重左大腿疼痛史,体格检查显示左大腿肿胀,尺寸为6x5厘米。该区域的x线显示混合溶解和硬化病变累及股骨头和颈部。计算机断层扫描显示混合性溶解性和硬化性病变累及股骨头和颈部,伴有皮质不规则和轻度骨膜反应,前部伴有相关软组织。磁共振成像显示非均匀信号强度病变伴股骨头及颈部硬化区。在T2W图像上,前部的大块相关软组织主要表现为高信号。在对比后的轴位和矢状位图像上,可以看到不均匀增强的软组织坏死区域。我们对尤文氏肉瘤和骨肉瘤进行了影像学鉴别诊断。然而,在组织病理学上,这是一例间充质软骨肉瘤。
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Mesenchymal Chondrosarcoma: A Rare Aggressive Variant of Chondrosarcoma
A 15-year-old boy reported a 2-month history of severe left thigh pain Physical examination revealed left thigh swelling measuring 6x5 cm. X-ray of the region showed mixed lytic and sclerotic lesion involving the femoral head and neck. A Computed Tomography scan showed mixed lytic and sclerotic lesion involving the femoral head and neck with cortical irregularity and mild periosteal reaction with associated soft tissue in the anterior aspect.  Magnetic resonance imaging demonstrated heterogeneous signal intensity lesion with areas of sclerosis involving the femoral head and neck. The large associated soft tissue in the anterior aspect appears predominantly hyperintense on T2W images. On post-contrast axial and sagittal images, heterogeneous enhancement with areas of necrosis involving soft tissue was seen. A presumptive radiological differential diagnosis of Ewing Sarcoma and Osteosarcoma was made. However, on histopathology, it was a case of mesenchymal chondrosarcoma.
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