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高位胸椎椎间盘突出症导致霍纳综合征并术中发现联合神经根受压:一例报告

High Thoracic Disc Herniation Causing Horner Syndrome with the Intraoperative Finding of Conjoined Nerve Root Compression: A Case Report.

作者信息

Bhandutia Amit K, Zuzek Zachary, Schessler Matthew J, Tomycz Nestor D, Altman Daniel T

机构信息

Departments of Orthopaedic Surgery (A.K.B., M.J.S., and D.T.A.) and Neurosurgery (N.D.T.), Allegheny General Hospital, Pittsburgh, Pennsylvania.

Drexel University College of Medicine, Philadelphia, Pennsylvania.

出版信息

JBJS Case Connect. 2017 Jan-Mar;7(1):e4. doi: 10.2106/JBJS.CC.16.00106.

Abstract

CASE

A 29-year-old man presented with right medial arm pain with paresthesia, as well as right-sided ptosis, miosis, and anhidrosis. Magnetic resonance imaging revealed a right paracentral disc herniation at the T1-T2 level. The patient underwent a hemilaminectomy with a medial facetectomy through a posterolateral approach to the T1-T2 disc space, followed by a discectomy. Intraoperative findings were notable for a conjoined nerve root.

CONCLUSION

Although high thoracic disc herniation is rare, its diagnosis should be considered when patients present with radicular arm pain and Horner syndrome. A high index of suspicion should be maintained for nerve root anomalies to limit iatrogenic injury and to ensure successful decompression.

摘要

病例

一名29岁男性出现右臂内侧疼痛伴感觉异常,以及右侧上睑下垂、瞳孔缩小和无汗。磁共振成像显示T1 - T2水平右侧中央旁椎间盘突出。患者通过后外侧入路对T1 - T2椎间盘间隙进行了半椎板切除术和内侧小关节切除术,随后进行了椎间盘切除术。术中发现有联合神经根。

结论

虽然高位胸椎椎间盘突出罕见,但当患者出现臂部放射性疼痛和霍纳综合征时,应考虑其诊断。对于神经根异常应保持高度怀疑,以限制医源性损伤并确保成功减压。

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