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Corrective surgery for kyphosis in a case of Gaucher's disease without history of vertebral compression fractures

机译:在没有椎体压缩骨折的情况下,在Gaucher病的情况下矫正手术

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摘要

Introduction: Gaucher's disease is a congenital metabolic disorder characterized by the accumulation of glucocerebroside in the reticuloendothelial system. Its clinical manifestations include splenomegaly, osteopenia, and pathological fractures. Cases of patients with kyphotic deformities caused by pathological vertebral compression fractures associated with Gaucher's disease are well reported. However, there has been no report regarding surgical treatment of kyphotic deformity caused by Gaucher's disease without compression fractures. In the present report, we describe surgical treatment for kyphotic deformity caused by Gaucher's disease without a past history of vertebral compression fractures.Case Report: The patient was diagnosed with Gaucher's disease at the age of 15 months. The patient was a 10-year-old girl with progressive kyphosis (84° between T6 and L3, with T12 as the apical vertebra) without compression fractures. Although the patient had been treated using a brace since the age of 3 years, the kyphosis progressed to the point where corrective surgery was required. We initially performed T3-L3 posterior spinal fusion, followed by anterior fusion 3 months later, which corrected the kyphosis to 35°. Postoperatively, the patient suffered fractures of the upper and lower extremities but did not have spinal fractures.Conclusions: Two-stage anterior/posterior combined correction and fusion was performed in a patient with kyphotic deformity caused by Gaucher's disease without compression fractures. Because of bone fragility in Gaucher's disease, careful selection of the fusion range and postoperative therapy was necessary.
机译:介绍:Gaucher的疾病是一种先天性代谢紊乱,其特征在于葡萄糖纤细胞在网状内皮系统中的积累。其临床表现包括脾肿大,骨质细胞和病理骨折。报道良好地报道了与Gaucher病相关的病理椎体压缩骨折引起的患者患者。然而,没有关于在没有压缩骨折的情况下由Gaucher疾病引起的凯氏畸形的手术治疗的报道。在本报告中,我们描述了Gaucher疾病引起的Kychic Deformity的手术治疗,没有过去的椎体压缩骨折史。Case报告:患者在15个月左右诊断出Gaucher疾病。患者是一名10岁的女孩,患有脑脊育脉(T6和L3之间的84°,T12为顶椎),没有压缩裂缝。虽然自3年以来,患者已经使用支架治疗,但脊柱氏症进入需要矫正手术的目的。我们最初进行了T3-L3后脊柱融合,然后3个月后融合,其校正了脊柱氏菌至35°。术后,患者遭受上肢和下肢的骨折,但没有脊柱骨折。结论:在没有压缩骨折的情况下,在患者中进行两阶段前/后部联合校正和融合。由于Gaucher疾病的骨脆弱,因此需要仔细选择融合范围和术后治疗。

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