Atypical Aggressive Hemangioma of Thoracic Vertebrae Associated With Thoracic Myelopathy-A Case Report and Review of the Literature.

IF 0.4 Q4 ORTHOPEDICS
Case Reports in Orthopedics Pub Date : 2024-08-13 eCollection Date: 2024-01-01 DOI:10.1155/2024/2307950
Krishna Timilsina, Sandesh Shrestha, Om Prakash Bhatta, Sushil Paudel, Rajesh Bahadur Lakhey, Rohit Kumar Pokharel
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引用次数: 0

Abstract

Aggressive thoracic hemangiomas are rare, benign tumors that extend into the spinal canal and cause neurological symptoms. Delayed diagnosis and treatment, due to a paucity of literature on optimal treatment strategies, can increase morbidity. This case report describes a 19-year-old male patient with aggressive thoracic hemangioma who presented with upper back pain and progressive weakness of the lower extremities. The patient underwent preoperative embolization and sclerotherapy, followed by decompression, posterior instrumentation, and stabilization. The final diagnosis was confirmed by biopsy, and there was a significant improvement in neurology after the surgical intervention. The diagnosis of rare lesions, such as aggressive hemangiomas, requires a high level of clinical suspicion and the assistance of imaging modalities in patients with features of compressive myelopathy. A combination of endovascular and surgical approaches can lead to optimal outcomes.

胸椎非典型侵袭性血管瘤伴胸椎脊髓病--病例报告和文献综述。
侵袭性胸血管瘤是一种罕见的良性肿瘤,会向椎管内延伸并引起神经症状。由于有关最佳治疗策略的文献很少,延误诊断和治疗会增加发病率。本病例报告描述了一名患有侵袭性胸血管瘤的 19 岁男性患者,他出现上背部疼痛和下肢进行性无力。患者术前接受了栓塞和硬化剂治疗,随后进行了减压、后方器械治疗和稳定。活组织检查证实了最终诊断,手术治疗后神经系统症状明显改善。对于具有压迫性脊髓病特征的患者,诊断侵袭性血管瘤等罕见病变需要高度的临床怀疑和影像学手段的辅助。将血管内治疗与手术治疗相结合,可以取得最佳疗效。
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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