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硬膜外类固醇注射后,一名患有未被识别的慢性特发性血小板减少性紫癜的患者因硬膜外血肿导致截瘫。

Paraplegia caused by an epidural hematoma in a patient with unrecognized chronic idiopathic thrombocytopenic purpura following an epidural steroid injection.

作者信息

Yoo Hyung Seok, Park Sung Wook, Han Jin Hee, Chung Jun Young, Yi Jae Woo, Kang Jong Man, Lee Bong Jae, Kim Dong Ok

机构信息

Department of Anesthesiology and Pain Medicine, College of Medicine, Kyung Hee University, Seoul, Korea.

出版信息

Spine (Phila Pa 1976). 2009 May 1;34(10):E376-9. doi: 10.1097/BRS.0b013e31819d0d45.

Abstract

STUDY DESIGN

Case report.

OBJECTIVES

To report a rare case of complicated paraplegia caused by a spontaneous epidural hematoma following an epidural steroid injection in a patient with unrecognized chronic idiopathic thrombocytopenic purpura (ITP) and to review relevant literature and discuss etiology, pathogenesis, and clinical features.

SUMMARY OF BACKGROUND DATA

A spinal epidural hematoma is a rare but potentially catastrophic complication, which could develop in patients without any risk factors. Some patients with chronic ITP are asymptomatic. To our knowledge there has been no previous report of such a complication.

METHODS

This is a retrospective review of a case seen at our institution.

RESULTS

The authors present a case of a 67-year-old woman who received an epidural steroid injection following complaints of lower back pain and bilateral buttock and leg pain. One day later, the patient had right leg numbness and weakness extending to her right knee; she was taken for emergency surgery. An emergency magnetic resonance imaging revealed an epidural hematoma with high-signal intensity on T2 imaging in the lumbar spinal cord and spinal cord compression with subdural hematoma. One week later, she was progressively developing lower extremity paraplegia with an L1 motor level and no sensory or sphincter activity. She was taken from the emergency room at our institution to the operating room for emergency decompression. After an uneventful course for 1 year, the patient presented with progressive bilateral lower extremity paralysis.

CONCLUSION

Epidural steroid therapy is a commonly used conservative therapy; however, complications could develop in patients without any risk factors. Clinicians who plan an epidural steroid injection must perform a rigorous evaluation through a detailed physical examination, simple laboratory tests, and history taking to prevent various risks associated with spinal cord compression.

摘要

研究设计

病例报告。

目的

报告1例在未识别出患有慢性特发性血小板减少性紫癜(ITP)的患者中,硬膜外类固醇注射后引发自发性硬膜外血肿导致复杂截瘫的罕见病例,并回顾相关文献,讨论病因、发病机制及临床特征。

背景资料总结

脊髓硬膜外血肿是一种罕见但可能具有灾难性的并发症,可在无任何危险因素的患者中发生。一些慢性ITP患者无症状。据我们所知,此前尚无此类并发症的报告。

方法

这是对我院所见1例病例的回顾性研究。

结果

作者报告1例67岁女性,因下背部疼痛及双侧臀部和腿部疼痛接受硬膜外类固醇注射。1天后,患者出现右腿麻木和无力,症状延伸至右膝;遂接受急诊手术。急诊磁共振成像显示腰椎脊髓T2加权像上有高信号强度的硬膜外血肿以及伴有硬膜下血肿的脊髓受压。1周后,她逐渐发展为下肢截瘫,运动平面为L1,无感觉或括约肌活动。她从我院急诊室被送往手术室进行急诊减压。经过1年的平稳病程后,患者出现进行性双侧下肢瘫痪。

结论

硬膜外类固醇治疗是一种常用的保守治疗方法;然而,在无任何危险因素的患者中也可能发生并发症。计划进行硬膜外类固醇注射的临床医生必须通过详细的体格检查、简单的实验室检查和病史采集进行严格评估,以预防与脊髓受压相关的各种风险。

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