Solitary Thoracic Exostosis Without Spinal Cord Compression Symptoms: A Rare Case Report

M. Shakeri, M. Chehrassan, Saeed Razi
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Abstract

Thoracic exostosis (osteochondroma) is rare. In this study, we report a rare case of thoracic exostosis in a 10-year-old boy arising in the T8 spinous process without expansion of mass to spinal canal. The patient’s parents noticed a mass in the dorsal aspect of the thorax for the past two years with gradual enlargement over six months. The patient had no clinical symptoms of spinal cord compression, such as pain and myelopathy. In the radiological evaluation, a calcified lesion was detected with the typical characteristics of exostosis. The lesion was removed with en bloc resection, and histologic examination confirmed the diagnosis of thoracic exostosis. The six-month follow-up of the patient showed the event-free survival. This study suggests the importance of early diagnosis and treatment of thoracic exostosis for preventing it from causing long-term neurological deficits and reducing its potential risk of malignant transformation.
无脊髓压迫症状的孤立性胸椎外生症:罕见病例报告
胸椎骨软骨瘤是罕见的。在这项研究中,我们报告了一例罕见的10岁男孩胸椎外生症,发生在T8棘突,肿块未扩张到椎管。患者的父母在过去两年中注意到胸背侧有肿块,并在六个月内逐渐增大。患者无脊髓压迫的临床症状,如疼痛和脊髓病。在放射学评估中,发现一个钙化病变,具有典型的外生性增生特征。病灶整体切除,病理检查证实为胸腔外生症。6个月的随访显示患者无事件生存。本研究提示早期诊断和治疗胸腔外生性增生对于防止其引起长期神经功能缺损和降低其恶性转化的潜在风险具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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