Kala Prakash Chandra, Dave Aniket, Katrolia Deepti, Saxena Suvinay, Poonia Dharma Ram
Department of Burns and Plastic Surgery, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.
Department of Diagnostic and Interventional Radiology, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.
J West Afr Coll Surg. 2025 Jan-Mar;15(1):92-96. doi: 10.4103/jwas.jwas_178_23. Epub 2024 Aug 2.
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 gene rearrangement are essential to confirm the diagnosis. Wide surgical excision and chemotherapy are the mainstay of managing neural EES.
神经内尤文肉瘤是一种极其罕见的肿瘤,文献中仅有少数孤立的病例报告。一名32岁的南亚男性出现了持续3个月的手腕和手指垂落症状。通过超声和磁共振成像进一步评估发现,手臂桡神经处有一个肿瘤。对肿瘤进行了广泛切除,并使用电缆状神经移植物重建了桡神经。使用免疫组织化学技术进行组织病理学评估后,确诊为骨外尤文肉瘤(EES)。患者随后接受了化疗,5个月后,他无病且无痛。然而,运动功能尚未恢复。临床检查结果和影像学检查有助于肿瘤的诊断和特征描述,但组织病理学和基因重排分析对于确诊至关重要。广泛的手术切除和化疗是治疗神经EES的主要方法。