Multistage surgical treatment of early-onset scoliosis in patients with Ehlers-Danlos syndrome: A series of observations

M. Mikhaylovskiy, V. A. Suzdalov
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Abstract

BACKGROUND: EhlersDanlos syndrome (EDS) is a group of hereditary pathological conditions caused by various disorders of collagen biosynthesis. The study analyzed the results of multistage surgical treatment of early scoliosis in patients with severe spinal deformities due to EDS. No similar observations have been found in the literature. CLINICAL CASES: Four patients with a verified diagnosis of EDS and progressive spinal deformities were subjected to multistage surgical treatment using the VEPTRII instrumentation, which included periodic distractions and final spinal fusion with segmental instrumentation. Stage-by-stage surgical treatment was initiated from the age of 3 to 6 years. In 3 of 4 cases, the kyphotic component prevailed over the scoliotic one (86140 vs. 21110). The number of staged distractions ranged from 6 to 10. The age of the final stage (correction and dorsal fusion) was 914 years (surgery was performed in three of four cases). The primary correction was 3056, the loss of correction before the final stage was 1435, and the correction during the final stage was 2240. A significant correction of the frontal and sagittal imbalances of the spine was noted. Blood loss during the final fusion was 540750 mL, and the operation time was 310350 min. Ten complications occurred, of which 9 were associated with implants and disappeared during staged distractions. No neurological and vascular complications occurred. DISCUSSION: Scoliosis occurring in the first decade of life in patients with EDS is characterized by early-onset, rapid progression, and tendency to form a significant kyphotic component of spinal deformity. CONCLUSIONS: Multistage treatment of early scoliosis in patients with EDS using VEPTRII tools allows for obtaining quite satisfactory results and has not severe complications. The final fusion gives a significant corrective effect; however, new research and accumulation of data are needed to optimize the treatment process.
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Ehlers-Danlos综合征患者早发性脊柱侧凸的多阶段手术治疗:一系列观察
背景:EhlersDanlos综合征(EDS)是一组由多种胶原生物合成障碍引起的遗传性病理疾病。本研究分析了EDS所致严重脊柱畸形患者早期脊柱侧凸的多阶段手术治疗结果。在文献中没有发现类似的观察结果。临床病例:4例确诊为EDS和进行性脊柱畸形的患者使用VEPTRII内固定进行了多阶段手术治疗,包括周期性分散和最后的脊柱融合节段内固定。从3岁到6岁开始分阶段进行手术治疗。在4例病例中,3例后凸成分优于脊柱侧凸成分(86140比21110)。分阶段分散注意力的次数从6到10不等。最后阶段(矫正和背侧融合)的年龄为914岁(4例中有3例进行了手术)。初级修正为3056,末期前修正损失为1435,末期修正为2240。我们注意到脊柱额位和矢状面不平衡的显著矫正。最终融合时失血量540750 mL,手术时间310350 min。共发生10例并发症,其中9例与种植体相关,在分阶段分心中消失。无神经和血管并发症发生。讨论:EDS患者10岁前发生脊柱侧凸的特点是起病早、进展快,并倾向于形成脊柱畸形的显著后凸成分。结论:使用VEPTRII工具对EDS患者的早期脊柱侧凸进行多阶段治疗,可获得相当满意的结果,且无严重并发症。最后的融合具有显著的矫正效果;然而,需要新的研究和数据的积累来优化处理过程。
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来源期刊
Pediatric Traumatology, Orthopaedics and Reconstructive Surgery
Pediatric Traumatology, Orthopaedics and Reconstructive Surgery Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.50
自引率
0.00%
发文量
38
期刊介绍: The target audience of the journal is researches, physicians, orthopedic trauma, burn, and pediatric surgeons, anesthesiologists, pediatricians, neurologists, oral surgeons, and all specialists in related fields of medicine.
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