儿童后路脊柱融合术后出现霍纳综合征：一例报告
Horner's syndrome after posterior spinal fusion in a child: a case report.
作者信息
Mueller K L, Loder R T, Eggenberger E R, Farley F A
机构信息
Section of Orthopaedic Surgery, Department of Surgery, University of Michigan Medical Center, Ann Arbor, Michigan, USA.
出版信息
Spine (Phila Pa 1976). 2000 Nov 1;25(21):2836-7. doi: 10.1097/00007632-200011010-00019.
STUDY DESIGN
A case report of a complication after posterior spinal fusion.
OBJECTIVES
To present the clinical findings of a Horner's syndrome after posterior spinal fusion.
SUMMARY OF BACKGROUND DATA
A 14-year-old girl underwent posterior spinal fusion for idiopathic scoliosis.
METHODS
Clinical examination and pharmacologic pupillary testing were used to diagnose Horner's syndrome.
RESULTS
After surgery, the patient developed a left-sided Horner's syndrome. The Horner's syndrome had resolved 6 months after surgery except for slight ptosis.
CONCLUSIONS
This is the first reported case of Horner's syndrome occurring after posterior spinal fusion without the use of epidural analgesia.
研究设计
一篇关于后路脊柱融合术后并发症的病例报告。
目的
介绍后路脊柱融合术后霍纳综合征的临床发现。
背景资料总结
一名14岁女孩因特发性脊柱侧弯接受了后路脊柱融合术。
方法
采用临床检查和药物瞳孔试验诊断霍纳综合征。
结果
术后患者出现左侧霍纳综合征。除轻度上睑下垂外，霍纳综合征在术后6个月已消退。
结论
这是首例报道的未使用硬膜外镇痛的后路脊柱融合术后发生霍纳综合征的病例。
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