Delayed paraparesis after posterior spinal fusion for congenital scoliosis: a case report

IF 0.7 Q4 CLINICAL NEUROLOGY Spinal Cord Series and Cases Pub Date : 2024-04-17 DOI:10.1038/s41394-024-00639-0
Shuhei Ohtsubo, Masayuki Ohashi, Toru Hirano, Hideki Tashi, Tatsuo Makino, Keitaro Minato, Yusuke Mitsuma, Hiroyuki Deguchi, Rintaro Hoshino, Nobuko Ohashi, Kenta Furutani, Hiroyuki Kawashima, Kei Watanabe
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Abstract

Introduction

Although multimodal intraoperative neuromonitoring (IONM), which has high sensitivity and specificity, is typically performed during spinal deformity surgery, neurological status may deteriorate with delay after surgical maneuvers. Here, we report a rare case of delayed postoperative neurological deficit (DPND) that was not detected by IONM during posterior spinal fusion (PSF) for congenital scoliosis.

Case presentation

A 14-year-old male presented with congenital scoliosis associated with T3 and T10 hemivertebrae. Preoperative Cobb angle of proximal thoracic (PT) and main thoracic (MT) curves were 50° and 41°, respectively. PSF (T1-L1) without hemivertebrectomy was performed, and the curves were corrected to 31° and 21° in the PT and MT curves, respectively, without any abnormal findings in IONM, blood pressure, or hemoglobin level. However, postoperative neurological examination revealed complete loss of motor function. A revision surgery, release of the curve correction by removing the rods, was immediately performed and muscle strength completely recovered on the first postoperative day. Five days postoperatively, PSF was achieved with less curve correction (36° in the PT curve and 26° in the MT curve), without postoperative neurological deficits.

Discussion

Possible mechanisms of DPND in our patient are spinal cord ischemia due to spinal cord traction caused by scoliosis correction and spinal cord kinking by the pedicle at the concave side. Understanding the possible mechanisms of intra- and postoperative neural injury is essential for appropriate intervention in each situation. Additionally, IONM should be continued to at least skin closure to detect DPND observed in our patient.

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先天性脊柱侧凸后路脊柱融合术后延迟性截瘫:病例报告
导言尽管多模态术中神经监测(IONM)具有很高的灵敏度和特异性,通常在脊柱畸形手术中进行,但手术操作延迟后神经状况可能会恶化。在此,我们报告了一例罕见的延迟性术后神经功能缺损(DPND)病例,该病例在先天性脊柱侧凸的后路脊柱融合术(PSF)中未被 IONM 检测到。术前胸椎近端(PT)和胸椎主弯(MT)的Cobb角分别为50°和41°。在未进行半椎体切除的情况下进行了PSF(T1-L1)手术,PT和MT曲线分别矫正为31°和21°,IONM、血压和血红蛋白水平均未发现异常。然而,术后神经系统检查发现,患者完全丧失了运动功能。立即进行了翻修手术,通过移除矫正杆解除了曲线矫正,术后第一天肌力就完全恢复了。术后五天,在较少的曲线矫正(PT曲线为36°,MT曲线为26°)的情况下实现了PSF,术后未出现神经功能缺损。讨论本例患者DPND的可能机制是脊柱侧凸矫正导致的脊髓牵引引起的脊髓缺血,以及凹侧椎弓根导致的脊髓扭转。了解术中和术后神经损伤的可能机制对于在各种情况下采取适当的干预措施至关重要。此外,IONM至少应持续到皮肤闭合,以检测在我们患者身上观察到的DPND。
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来源期刊
Spinal Cord Series and Cases
Spinal Cord Series and Cases Medicine-Neurology (clinical)
CiteScore
2.20
自引率
8.30%
发文量
92
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