跟骨软骨粘液样纤维瘤1例

Shekar Mudramaiah, Pavith Janardhan T, Ajay Krishna
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引用次数: 0

摘要

软骨粘液样纤维瘤是一种罕见的发生于跟骨的良性原发性肿瘤。我们报告一例23岁的女性,有3个月的突然发作的右脚跟疼痛史,没有外伤史。走路和站立等运动加剧了这种情况。右脚和脚踝的x线检查显示跟骨后部有病变。对跟骨进行MRI扫描,发现有边界清晰的溶解性病变。病变采用刮除、髂骨移植和骨水泥治疗。术后3个月,骨水泥将移植物固定。在一年的随访中没有复发的迹象,患者踝关节活动范围足够。尽管这种肿瘤很少见,但医生还是有必要认识到它的放射学特征,并提供适当的治疗方案。关键词:软骨粘液样纤维瘤,溶解性病变,良性原发肿瘤
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Case of Chondromyxoid Fibroma of Calcaneum: A Case Report
Chondromyxoid fibroma is a rare benign Primary tumour occurring in the calcaneum. We report a case of a 23-year-old woman with 3 months history of sudden onset right heel pain with no history of trauma. Which was exacerbated by movement such as walking and standing. A radiographic examination of the right foot and ankle revealed a lesion in the posterior part of the calcaneum. The calcaneum was further evaluated using an MRI scan which revealed a lytic lesion with clearly defined borders. The lesion was treated with curettage, iliac bone grafting, and cementing. Three months after surgery, the graft was consolidated with bone cement in place. There was no sign of recurrence at the one-year follow-up, and the patient had adequate ankle range of motion. Even though the tumour is rare, there is a need for physicians to recognize its radiological features and offer appropriate treatment options. Keywords: Chondromyxoid fibroma, Lytic lesion, Benign primary tumour
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