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Severe kyphoscoliosis after primary Echinococcus granulosus infection of the spine

机译:脊柱原发性棘球chin虫感染后严重脊柱后凸

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摘要

A primary Echinococcus granulosus infection of the spine involving the vertebrae T8 and T9 of a 6-year-old child was treated elsewhere by thoracotomy, partial corporectomy, multiple laminectomies and uninstrumented fusion. Owing to inappropriate stabilization, severe deformity developed secondary to these surgeries. X-rays, CT and MRI scans of the spine revealed a severe thoracic kyphoscoliosis of more than 100° (Fig. ) and recurrence of Echinococcus granulosus infection. The intraspinal cyst formation was located between the stretched dural sac and the vertebral bodies of the kyphotic apex causing significant compression of the cord (Figs. , , ). A progressive neurologic deficit was reported by the patient. At the time of referral, the patient was wheelchair bound and unable to walk by herself (Frankel Grade C). Standard antiinfectious therapy of Echinococcus granulosus requires a minimum treatment period of 3 months. This should be done before any surgical intervention because in case of a rupture of an active cyst, the delivered lipoprotein antigens of the parasite may cause a potentially lethal anaphylactic shock. Owing to the critical neurological status, we decided to perform surgery without full length preoperative antiinfectious therapy. Surgical treatment consisted in posterior vertebral column resection technique with an extensive bilateral costotransversectomy over three levels, re-decompression with cyst excision around the apex and multilevel corporectomy of the apex of the deformity. Stabilisation and correction of the spinal deformity were done by insertion of a vertebral body replacement cage anteriorly and posterior shortening by compression and by a multisegmental pedicle screw construct. After the surgery, antihelminthic therapy was continued. The patients neurological deficits resolved quickly: 4 weeks after surgery, the patient had Frankel Grade D and was ambulatory without any assistance. After an 18-month follow-up, the patient is free of recurrence of infection and free of neurologically deficits (Frankel E). This case demonstrates that inappropriate treatment—partial resection of the cyst, inappropriate anterior stabilization and posterior multilevel laminectomies without posterior stabilization—may lead to severe progressive kyphoscoliotic deformity and recurrence of infection, both leading to significant neurological injury presenting as a very difficult to treat pathology.X-rays of the patient showing a kyhoscoliotic deformity. >a ap view, >b lateral view
机译:通过开胸手术,部分肾切除术,多发椎板切除术和非器械融合术治疗了原发性棘球gran虫感染的脊椎棘突,涉及一名6岁儿童的椎骨T8和T9。由于不适当的稳定,这些手术继发了严重的畸形。脊柱的X射线,CT和MRI扫描显示,严重的胸椎后凸畸形超过100°(图),并再次感染了细粒棘球E虫。脊柱内囊肿的形成位于伸直的硬膜囊和脊柱后凸的椎体之间,导致脐带明显受压(图,,)。患者报告有进行性神经功能缺损。转诊时,患者被轮椅束缚,无法独自行走(Frankel C级)。细粒棘球oc的标准抗感染治疗要求至少3个月的治疗期。这应该在任何外科手术之前进行,因为如果活动性囊肿破裂,所递送的寄生虫脂蛋白抗原可能会引起潜在的致死性过敏性休克。由于神经系统处于危急状态,我们决定在不进行全长术前抗感染治疗的情况下进行手术。手术治疗包括椎管后路切除术,三级以上广泛双侧肋横突切除术,再减压,根尖周围囊肿切除和畸形根尖多层切除术。脊椎畸形的稳定和矫正是通过向前插入椎体置换笼,并通过压缩和多节椎弓根螺钉构造来缩短后壁。手术后,继续进行抗蠕虫治疗。患者的神经功能缺损很快得到解决:手术后4周,患者患有Frankel D级,无需任何帮助就可以走动。经过18个月的随访,患者无感染复发,无神经功能缺损(Frankel E)。该病例表明,不适当的治疗(部分切除囊肿,不适当的前路稳固和后路多级椎板切开术而无后路稳固)可能导致严重的进行性脊柱后凸畸形和感染复发,均导致严重的神经系统损伤,这是非常难以治疗的病理。<!-fig ft0-> <!-fig mode = art f1-> <!-说明a7->患者的X射线显示出颈缩性畸形。 > a ap视图,> b 侧视图

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