Sharma Aadhar, Brown Kate, Skinner John, Whelan Jeremy, Fox Michael
Peripheral Nerve Injury Unit, Royal National Orthopaedic Hospital, Stanmore, Middlesex HA7 4LP, UK.
Sarcoma Unit, Royal National Orthopaedic Hospital, Stanmore, Middlesex HA7 4LP, UK.
Case Rep Surg. 2015;2015:172635. doi: 10.1155/2015/172635. Epub 2015 Jul 8.
Ewing's sarcoma is a common bone tumour of childhood but is a rare occurrence in individuals over 20 years of age. Few cases are reported as originating from peripheral nerves. We present an unusual case of extraosseous Ewing's sarcoma originating from the sciatic nerve in a 66-year-old patient which had the clinical hallmarks of a benign nerve sheath tumour. Following discussion at a multidisciplinary meeting, excision biopsy of the suspected benign nerve sheath tumour was planned. At operation, the mass had malignant features. Histology confirmed the presence of Ewing's sarcoma. Due to the morbidity of nerve resection, radiotherapy and chemotherapy were commenced. Ewing's sarcoma is known to mimic benign pathologies. In this case there were subtle signs of a malignant process in the form of unremitting pain. It is vital to keep in mind the less common tumours that can affect the peripheral nervous system in such cases.
尤因肉瘤是儿童期常见的骨肿瘤,但在20岁以上的个体中很少见。很少有病例报告起源于周围神经。我们报告一例罕见的骨外尤因肉瘤,起源于一名66岁患者的坐骨神经,具有良性神经鞘瘤的临床特征。在多学科会议讨论后,计划对疑似良性神经鞘瘤进行切除活检。手术中,肿块具有恶性特征。组织学检查证实为尤因肉瘤。由于神经切除的并发症,开始进行放疗和化疗。已知尤因肉瘤可模仿良性病变。在本例中,以持续疼痛的形式存在恶性病变的细微迹象。在这种情况下,牢记可能影响周围神经系统的罕见肿瘤至关重要。