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首页> 外文期刊>World neurosurgery >Transpedicular Excision of a Thoracic Intraspinal Osteochondroma in a Patient with Hereditary Multiple Exostoses and Brown-Séquard Syndrome
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Transpedicular Excision of a Thoracic Intraspinal Osteochondroma in a Patient with Hereditary Multiple Exostoses and Brown-Séquard Syndrome

机译:患有遗传多重消除的患者胸腔内骨孔瘤和棕色 - Séquard综合征的胸腔内骨吸粒细胞横向切除

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摘要

BackgroundSpinal osteochondroma is a rare but recognized cause of myelopathy. Brown-Séquard syndrome is a form of severe myelopathy characterized by a clinical picture of hemisection of the spinal cord. Brown-Séquard syndrome caused by osteochondroma is extremely rare, calling for individualized surgical procedures. Case DescriptionWe report a 16-year-old girl with hereditary multiple exostoses and a rare case of thoracic osteochondroma causing partial Brown-Séquard syndrome. Customized surgical procedures were designed to avoid iatrogenic spinal cord injury. The patient underwent neural decompression and tumor excision through a transpedicular approach. The surgical procedure consisted of 4 consecutive steps: 1) laminectomy, 2) costotransversectomy and pediculectomy, 3) extracavitary removal of the mass, and 4) pedicular fixation with fusion. Total resection of the tumor was achieved macroscopically without intraoperative spinal cord injury. The postoperative recovery was uneventful, and the patient returned to a normal life without evidence of recurrence at 24-month follow-up. ConclusionsFor patients with hereditary multiple exostosis and new onset of neurologic symptoms, the possibility of a spinal osteochondroma should be considered. In the situation of an intraspinal exostosis protruding from the lateral side, customized surgical procedures with a transpedicular approach may be a valid way to minimize intraoperative neural injury and achieve a satisfactory outcome.
机译:背景骨骨质瘤是一种罕见但公认的肌钙病。 Brown-Séquard综合征是一种严重的肌鲸病,其特征在于脊髓的半切割的临床图。由骨孔瘤引起的布朗 - Quard综合征极为罕见,呼吁个体外科手术。案例描述我们举报了一个16岁的女孩,遗传多重遗传,罕见的胸骨骨粒细胞癌导致部分棕色核心综合征。定制的外科手术被设计为避免来自科学脊髓损伤。患者通过横向方法接受神经减压和肿瘤切除。外科手术包括4步:1)椎板切除术,2)克莱乳糖切除术和PeICulectomy,3)骨干扰去除质量,4)钉钉固体固定。肿瘤的总切除术在宏观上均衡而没有术目不然脊髓损伤。术后回收是不行的,患者恢复正常生活,没有24个月随访的复发证据。结论患有遗传性多源性症状的患者和神经系统症状的新发病,应考虑脊髓骨孔瘤的可能性。在从横向侧突出的内侧脱模的情况下,具有床突方法的定制外科手术可能是最大限度地减少术中神经损伤并实现令人满意的结果的有效方法。

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