由 IgG4 相关肥大性脊髓膜炎引起的颈椎脊髓病:病例报告和文献综述。

IF 1.9 Q3 CLINICAL NEUROLOGY
Brain & spine Pub Date : 2024-09-10 eCollection Date: 2024-01-01 DOI:10.1016/j.bas.2024.103325
Ahmet Parlak, Christian-Andreas Mueller, Kay W Nolte, Tobias P Schmidt, Ulf Bertram, Hans Clusmann, Christian Blume
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引用次数: 0

摘要

简介IgG4 相关疾病是一种以 IgG4 阳性浆细胞的组织浸润为特征的免疫介导疾病。脊髓膜受累导致肥厚性脊髓膜炎(HSP),引起脊髓和神经根受压:在这篇综述中,我们介绍了一例与 IgG4 相关的肥厚性脊髓膜炎病例。此外,我们还提供了有关 IgG4 相关 HSP 的最新文献综述:我们描述了一例 45 岁男性颈椎病患者的病例。磁共振成像显示脑膜腹背侧增厚,导致脊髓受压。患者接受了椎板切除术减压,并切除了增厚的硬脑膜。病理结果显示患者患有肥厚性脑膜脑炎,进一步检查显示硬脑膜有大量 IgG4 阳性淋巴细胞浸润。使用甲基强的松龙和利妥昔单抗进行辅助治疗后,患者的神经功能完全恢复,术后12个月核磁共振成像和临床检查均未发现复发迹象。相关文章在 PubMed、Web of Science 和 Embase 数据库中进行了检索。结果:文献综述总结了52个现有病例,其中包括本中心的1个病例。在28例患者(58%)中观察到了神经功能损害的进行性恶化。病变涉及胸椎(33 例,62.2%)、颈椎(35 例,70%)、腰椎(10 例,20%)和骶椎(1 例,2.2%)。硬膜增厚通常表现为条纹状、纺锤形或椭圆形改变,其中同质和同型改变最为常见。治疗的主要选择是手术减压,然后进行免疫抑制治疗。有一例病例最终死亡:讨论和结论:IgG4 相关 HSP 通常会影响颈部和胸部硬脑膜,因此常常表现为脊髓病变。在出现神经功能缺损的病例中,手术减压可避免永久性神经损伤。免疫抑制疗法是治疗 IgG4 相关 HSP 的基石。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cervical myelopathy caused by IgG4-related hypertrophic spinal pachymeningitis: Case report and a descriptive review of the literature.

Introduction: IgG4-related disease is an immune-mediated condition characterized by tissue infiltration of IgG4-positive plasma cells. Involvement of the spinal meninges results in hypertrophic spinal pachymeningitis (HSP), causing spinal cord and nerve root compression.

Research question and case description: In this review, we present a case of IgG4-related hypertrophic spinal pachymeningitis. Furthermore, we provide an updated literature review on IgG4-related HSP.

Materials and methods: We describe the case of a 45-year-old male presenting with cervical myelopathy. MR-imaging showed a ventrodorsal thickening of the meninges resulting in spinal cord compression. The patient underwent surgical decompression through laminectomy and excision of the dural thickening. The pathological findings demonstrated hypertrophic pachymeningitis with further examination showing large-scale dural infiltration of IgG4-positive lymphocytes. Adjuvant therapy with methylprednisolone and rituximab resulted in full neurological recovery with no signs of recurrence on MRI or clinically 12 months postoperatively.An updated review of the literature regarding IgG4-related HSP was performed according to PRISMA-guidelines. Relevant articles were searched from the PubMed, Web of Science and Embase databases. Patient characteristics, MRI- and histopathological findings, treatment modality and outcome were reviewed.

Results: The literature review provided a summary of 52 available cases, which included the one cases from our centre. Progressive worsening of neurological impairment was observed in 28 patients (58%). The lesions involved the thoracic spine (n = 33, 62.2%), cervical spine (n = 35, 70%), lumbar spine (n = 10, 20%), and sacral spine (n = 1, 2.2%). The dural thickening typically appeared as striated, fusiform, or oval changes, with homogeneous and patterns being the most common. Surgical decompression followed by immunosuppressive treatment was the main choice of therapy. The disease proved fatal in one case.

Discussion and conclusion: IgG4-related HSP usually affects the cervical and thoracic dura and therefore often presents with myelopathy. Surgical decompression in cases of neurological deficits may prevent permanent neurological impairment. Immunosuppressive therapy constitutes the cornerstone in the treatment IgG4-related HSP.

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来源期刊
Brain & spine
Brain & spine Surgery
CiteScore
1.10
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71 days
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