Intra-neural Ewing Sarcoma of the Radial Nerve Presenting as Wrist.

Prakash Chandra Kala, Aniket Dave, Deepti Katrolia, Suvinay Saxena, Dharma Ram Poonia
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Abstract

Intra-neural Ewing sarcoma is an extremely rare tumour and only a few isolated case reports exist in the literature. A 32-year-old South Asian male presented with wrist and finger drops of 3 months duration. Further evaluation with ultrasonography and magnetic resonance imaging revealed a tumour of the radial nerve in the arm. A wide excision of the tumour was performed, and the radial nerve was reconstructed with cabled nerve grafts. A diagnosis of extra-osseous Ewing sarcoma (EES) was made after histopathological evaluation using immunohistochemistry techniques. The patient subsequently received chemotherapy and after 5 months, he is disease-free and pain-free. However, there has been no motor recovery yet. Clinical findings and imaging can help and characterise the tumour, but histopathology and analysis for EWSR1 gene rearrangement are essential to confirm the diagnosis. Wide surgical excision and chemotherapy are the mainstay of managing neural EES.

桡神经内尤文氏肉瘤表现为腕部。
神经内尤文氏肉瘤是一种极为罕见的肿瘤,文献中只有少数孤立的病例报告。32岁南亚男性,手腕和手指滴液持续3个月。进一步的超声检查和磁共振成像显示手臂桡神经肿瘤。大面积切除肿瘤,用带索神经移植物重建桡神经。采用免疫组织化学技术进行组织病理学评估后诊断为骨外尤文氏肉瘤(EES)。患者随后接受化疗,5个月后无病无痛。然而,还没有运动恢复。临床表现和影像学可以帮助确定肿瘤的特征,但组织病理学和EWSR1基因重排分析对于确认诊断至关重要。广泛的手术切除和化疗是治疗神经性EES的主要方法。
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