Ushijima Takahiro, Kawaguchi Kenichi, Matsumoto Tadashi, Takagi Masaki, Kondoh Tatsuro, Nishimura Gen, Iida Aritoshi, Ikegawa Shiro, Haga Nobuhiko, Kato Go
Department of Spine Surgery, Saga Medical Centre, Koseikan, 400 Nakabaru Kase-Machi, Saga, 840-8571, Japan.
Department of Trauma Centre, Saga Medical Centre, Koseikan, 400 Nakabaru Kase-Machi, Saga, 840-8571, Japan.
BMC Res Notes. 2018 Feb 7;11(1):106. doi: 10.1186/s13104-018-3227-7.
Patients with ankylosing spines are susceptible to developing spinal fractures even with minor trauma and can develop early or late neurological injuries. These fractures require early and aggressive surgical management to enable spinal stability and/or neural decompression. Being highly unstable by nature, they require relatively long segment instrumentation and fusion, which can increase paravertebral soft tissue damage and perioperative bleeding. The purpose of this report is to describe a rare case of traumatic double fractures at the cervico-thoracic and thoraco-lumbar transition zones in ankylosing spine with spondylo-epiphyseal dysplasia (SED) of unknown cause, which were successfully treated with a combined open and percutaneous spinal fusion procedure.
A 46-year-old woman who was diagnosed with non-contiguous fractures in cervico-thoracic and thoraco-lumbar junction zones among multiple injuries sustained in a traffic accident was treated with hybrid techniques for posterior instrumentation with an open approach using a computed tomography (CT)-based navigation system and percutaneous pedicle-screwing method. She regained mobility to pre-admission levels and started walking on crutches 3 months postoperatively. Genetic testing for the cause of SED revealed no mutation in the COL2A1 or TRPVR4 genes. The union of fractured spine was confirmed on CT scan 1 year postoperatively.
This is the first report of double spinal fractures in an ankylosing spine with genetically undetermined spondyloepiphyseal dysplasia. A long-segment posterior instrumentation procedure incorporating the invasive treatment of spinal fractures in ankylosing spondylitis or diffuse idiopathic hyperostosis was effective.
强直性脊柱炎患者即使受到轻微创伤也易发生脊柱骨折,并可能出现早期或晚期神经损伤。这些骨折需要早期积极的手术治疗以实现脊柱稳定和/或神经减压。由于本质上高度不稳定,它们需要相对较长节段的内固定和融合,这会增加椎旁软组织损伤和围手术期出血。本报告的目的是描述一例罕见的强直性脊柱炎合并原因不明的脊椎骨骺发育不良(SED)患者,在颈胸和胸腰交界区发生创伤性双骨折,并通过开放与经皮脊柱融合联合手术成功治疗的病例。
一名46岁女性在交通事故中多处受伤,被诊断为颈胸和胸腰交界区非连续性骨折,采用基于计算机断层扫描(CT)导航系统的开放入路和经皮椎弓根螺钉置入法的混合技术进行后路内固定治疗。她术后3个月恢复到入院前的活动能力并开始拄拐行走。对SED病因进行的基因检测显示COL2A1或TRPVR4基因无突变。术后1年CT扫描证实骨折脊柱愈合。
这是首例关于强直性脊柱炎合并基因未明的脊椎骨骺发育不良患者发生双脊柱骨折的报告。采用包括强直性脊柱炎或弥漫性特发性骨肥厚脊柱骨折侵入性治疗的长节段后路内固定手术是有效的。