李晨恺, 王升儒, 李子全, 吴南, 仉建国. Gorham-Stout综合征合并脊柱侧后凸一例[J]. 罕见病研究, 2023, 2(4): 602-606. DOI: 10.12376/j.issn.2097-0501.2023.04.016
引用本文: 李晨恺, 王升儒, 李子全, 吴南, 仉建国. Gorham-Stout综合征合并脊柱侧后凸一例[J]. 罕见病研究, 2023, 2(4): 602-606. DOI: 10.12376/j.issn.2097-0501.2023.04.016
LI Chenkai, WANG Shengru, LI Ziquan, WU Nan, ZHANG Jianguo. A Case Report of Gorham-Stout Syndrome with Kyphoscoliosis[J]. Journal of Rare Diseases, 2023, 2(4): 602-606. DOI: 10.12376/j.issn.2097-0501.2023.04.016
Citation: LI Chenkai, WANG Shengru, LI Ziquan, WU Nan, ZHANG Jianguo. A Case Report of Gorham-Stout Syndrome with Kyphoscoliosis[J]. Journal of Rare Diseases, 2023, 2(4): 602-606. DOI: 10.12376/j.issn.2097-0501.2023.04.016

Gorham-Stout综合征合并脊柱侧后凸一例

A Case Report of Gorham-Stout Syndrome with Kyphoscoliosis

  • 摘要: 本文报道1例Gorham-Stout综合征(GSS)合并脊柱侧后凸患者的治疗过程。患者男性,11岁,发现脊柱侧后凸4年,加重伴双下肢无力1年。患者同时合并乳糜胸、通气功能障碍和骨质疏松。患者曾于外院接受颅骨牵引术治疗7月余,效果不佳;最终,患者于我院接受后路脊柱侧后凸矫形、内固定、植骨融合术(C4-T8),术后临床疗效良好,矫形满意,双下肢不全瘫明显改善。本文通过典型病例报道及既往文献回顾,以期提高临床医师对该疾病的认识,并为该疾病的诊治提供借鉴。

     

    Abstract: This article reported the treatment of Gorham Stout syndrome (GSS) with kyphoscoliosis. The patient was an 11-year-old male who was presented with kyphoscoliosis, first developed 4 years ago, accompanied by incomplete paralysis of both lower limbs. The syndrome worsened in the previous year. He had a history of chylothorax, ventilation dysfunction, and osteoporosis. The patient underwent skull traction in another hospital for 7 months, which was ineffective. Finally, he underwent posterior correction, internal fixation, and bone graft fusion (C4-T8) in our hospital. The postoperative clinical outcomes and the posterior correction were satisfactory, with significant improvement in incomplete paralysis of both lower limbs. This article aims to improve the understanding of GSS and provided reference for its diagnosis and treatment through a typical case report and review of previous literature.

     

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