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合并短暂性单侧肌无力的颈段脊髓髓内结节病的外科治疗:一例报告

Surgical management of intramedullary cervical spinal sarcoidosis complicated by transient unilateral weakness: A case report.

作者信息

Saade Aziz, Denwood Hayley M, Tannoury Tony, Tannoury Chadi

机构信息

Department of Orthopaedic Surgery, University of California Davis Medical Center, Sacramento, California, United States.

Department of Orthopedic Surgery, Boston Medical Center, One Boston Medical Center Place, Boston, Massachusetts, United States.

出版信息

Surg Neurol Int. 2024 Mar 8;15:76. doi: 10.25259/SNI_41_2024. eCollection 2024.

Abstract

BACKGROUND

Sarcoidosis, a multisystem inflammatory non-caseating granulomatous disease, can present with neurologic lesions in up to 10% of patients.

CASE DESCRIPTION

A 57-year-old male presented with three months of worsening upper extremity radicular pain associated with dysmetria, hyperreflexia, bilateral Hoffman's, and positive Babinski signs. The contrast magnetic resonance imaging (MRI) showed a diffuse T2 signal hyperintensity and T1-enhancing 2.5 cm lesion extending sagittally between C4 and C6. The cerebrospinal fluid analysis showed a high protein level and lymphocytic pleocytosis. A cardiac positron emission tomography scan was consistent with the diagnosis of cardiac sarcoidosis. With the diagnosis of multisystemic/probable neurosarcoidosis, the patient was unsuccessfully treated with intravenous methylprednisolone, followed by infliximab. Due to severe cord compression/myelopathy, a C3-C6 laminectomy and C3-C7 posterior spinal fusion were performed. Postoperatively, the patient developed a transient right-sided hemiparesis. Over nine postoperative months, the patient had four relapses of transient repeated episodes of paresis, although follow-up cervical MRI scans revealed adequate cord decompression with a stable intramedullary hyperintense lesion.

CONCLUSION

Patients with neurosarcoidosis respond unpredictably to surgical decompression and require prolonged medical care, which is often unsuccessful.

摘要

背景

结节病是一种多系统炎症性非干酪样肉芽肿性疾病,高达10%的患者可出现神经病变。

病例描述

一名57岁男性,出现三个月来逐渐加重的上肢神经根性疼痛,伴有共济失调、反射亢进、双侧霍夫曼征阳性及巴宾斯基征阳性。对比增强磁共振成像(MRI)显示在C4和C6之间有一个2.5 cm的病变,呈弥漫性T2信号高增强和T1增强,纵向延伸。脑脊液分析显示蛋白水平升高和淋巴细胞增多。心脏正电子发射断层扫描与心脏结节病的诊断一致。在诊断为多系统/可能的神经结节病后,患者接受静脉注射甲泼尼龙治疗,随后使用英夫利昔单抗治疗,但均未成功。由于严重的脊髓压迫/脊髓病,进行了C3-C6椎板切除术和C3-C7后路脊柱融合术。术后,患者出现短暂的右侧偏瘫。术后九个月内,患者出现四次短暂性反复轻瘫发作的复发,尽管随访颈椎MRI扫描显示脊髓减压充分,髓内高信号病变稳定。

结论

神经结节病患者对手术减压的反应不可预测,需要长期医疗护理,且往往不成功。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f1d/11021060/9e58102f563b/SNI-15-76-g001.jpg

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