Neuromuscular scoliosis as a sequelae of Guillain-Barre syndrome

被引:3
作者
Edwards, Max R. [1 ]
Panteliadis, Pavlos [1 ]
Lucas, Jonathan D. [1 ]
机构
[1] Guys & St Thomas NHS Trust, Dept Spinal Surg, London SE1 9RT, England
来源
JOURNAL OF PEDIATRIC ORTHOPAEDICS-PART B | 2010年 / 19卷 / 01期
关键词
Guillain-Barre syndrome; Miller-Fisher variant; neuromuscular; scoliosis;
D O I
10.1097/BPB.0b013e32832efca2
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
The neuromuscular sequaelae of Guillain-Barre syndrome are well documented in the literature. Persistent distal muscular weakness and loss of peripheral limb reflexes are common in those affected. We report a case of a 14-year-old boy who developed the Miller-Fisher variant of Guillain-Barre syndrome at the age of 8 years. Six years after the acute episode, he had persistent lower limb areflexia and mild weakness. Fie had also developed a neuromuscular scoliosis. The scoliosis was successfully treated with posterior instrumentation and fusion surgery. Neuromuscular scoliosis is rare following Guillain-Barre syndrome, with no previous reports associated with the Miller-Fisher variant that we are aware of. When evaluating patients post Guillain-Barre syndrome, structural spinal examination is essential to identify rare deformity that may need surgical correction. J Pediatr Orthop B 19:95-97 (C) 2010 Wolters Kluwer Health | Lippincott Williams & Wilkins.
引用
收藏
页码:95 / 97
页数:3
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