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家族性自主神经功能异常中的脊柱侧弯。手术治疗。

Scoliosis in familial dysautonomia. Operative treatment.

作者信息

Rubery P T, Spielman J H, Hester P, Axelrod E, Burke S W, Levine D B

机构信息

Hospital for Special Surgery, New York Hospital-Cornell University Medical College, New York City, USA.

出版信息

J Bone Joint Surg Am. 1995 Sep;77(9):1362-9. doi: 10.2106/00004623-199509000-00012.

DOI:10.2106/00004623-199509000-00012
PMID:7673287
Abstract

The results of operative treatment of scoliosis were reviewed for twenty-two patients (ten boys and twelve girls) who had familial dysautonomia, an autosomal recessive disorder affecting primarily Ashkenazi Jews. The indication for operative intervention was progressive kyphoscoliosis to 45 degrees or more in a skeletally immature patient for whom bracing had failed. The mean age at the time of the operation was fifteen years and five months (range, eight years and two months to nineteen years). Seventeen patients had a thoracic curve with a mean preoperative Cobb angle of 69 degrees (range, 47 to 112 degrees), and five patients had a double major curve with a mean preoperative Cobb angle of 71 degrees (range, 42 to 87 degrees) for the cephalad curves and 60 degrees (range, 45 to 72 degrees) for the caudad curves. Twenty patients had a rigid kyphosis; in fourteen, the apex was at the seventh thoracic vertebra or more cephalad. Two patients had a lordoscoliosis. The mean preoperative kyphosis was 64 degrees (range, 12 to 110 degrees) in the thirteen patients who had a thoracic curve and for whom information regarding kyphosis was available, and it was 70 degrees (range, 54 to 84 degrees) in the five patients who had a double major curve. Postoperior spinal arthrodesis and instrumentation was performed in all patients. Two patients had an anterior arthrodesis as well because of the severity and rigidity of the curve. Allograft bone was used in eighteen patients. Postoperatively, all patients were managed with a body cast or with a custom-molded thoracolumbar brace.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对22例患有家族性自主神经功能异常的患者(10名男孩和12名女孩)的脊柱侧弯手术治疗结果进行了回顾。家族性自主神经功能异常是一种常染色体隐性疾病,主要影响德系犹太人。手术干预的指征是骨骼未成熟且支具治疗失败、进展性脊柱后凸侧弯达到45度或以上的患者。手术时的平均年龄为15岁零5个月(范围为8岁零2个月至19岁)。17例患者有胸段侧弯,术前Cobb角平均为69度(范围为47至112度),5例患者有双主弯,头侧弯术前Cobb角平均为71度(范围为42至87度),尾侧弯术前Cobb角平均为60度(范围为45至72度)。20例患者有僵硬性脊柱后凸;其中14例顶点位于第7胸椎或更靠头侧。2例患者有脊柱前凸侧弯。在有胸段侧弯且可获得脊柱后凸信息的13例患者中,术前脊柱后凸平均为64度(范围为12至110度),在有双主弯的5例患者中,术前脊柱后凸平均为70度(范围为54至84度)。所有患者均进行了后路脊柱融合术和器械固定。由于侧弯严重且僵硬,2例患者还进行了前路融合术。18例患者使用了同种异体骨。术后,所有患者均使用石膏背心或定制的胸腰段支具进行治疗。(摘要截短至250字)

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A rating scale for the functional assessment of patients with familial dysautonomia (Riley Day syndrome).用于评估家族性自主神经异常症(Riley Day 综合征)患者功能的评定量表。
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