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马尾神经结节病:临床病程、影像学和电诊断结果、治疗反应和结局。

Neurosarcoidosis of the Cauda Equina: Clinical Course, Radiographic and Electrodiagnostic Findings, Response to Treatment, and Outcomes.

机构信息

From the Neurology Residency Program (G.A.B.), and Division of Neuromuscular Medicine (R.G.-S.), Department of Neurology, Division of Neuroradiology (A.J.C.), Department of Radiology, and Division of Hospital Neurology (S.K.H.), Department of Neurology, Emory University School of Medicine, Atlanta, GA.

出版信息

Neurol Neuroimmunol Neuroinflamm. 2022 Apr 29;9(4). doi: 10.1212/NXI.0000000000001170. Print 2022 Jul.

Abstract

BACKGROUND AND OBJECTIVES

Sarcoidosis is a multisystem granulomatous disease affecting the nervous system in 3%-5% of cases. It can affect almost any component of the nervous system. Involvement of the cauda equina is an understudied phenotype, and questions remain regarding its natural history and optimal approach to management. This study aims to study the long-term clinical evolution of neurosarcoidosis affecting the cauda equina, response to treatment, and clinical and radiographic outcomes.

METHODS

Patients with neurosarcoidosis treated at Emory University between January 1, 2011, and December 8, 2021, were retrospectively evaluated for manifestations of cauda equina disease and included if disease of the cauda equina could be substantiated by MRI or EMG.

RESULTS

Of 216 cases, 14 (6.5%) involved the cauda equina. The median age was 49.5 years, and most were female (85.7%) and African American (64.3%). Chronic (>28 days) presentations were most common (78.6%), but acute (<7 days, 14.3%) and subacute (7-28 days, 7.1%) were also seen. The median modified Rankin Scale (mRS) score at nadir was 3 (range 2-4). Symptoms were asymmetric in 78.6% and included leg numbness (85.7%), leg weakness (64.3%), perineal numbness (35.7%), pain (42.3%), and incontinence (21.4%). On MRI, the cauda equina enhanced in 100%, appeared nodular in 78.6%, and was diffusely involved in 71.4%. Coexisting myelitis was common (cervical 28.6%, thoracic 35.7%, and conus medullaris 28.6%). Intracranial inflammation included leptomeningitis (71.4%) and cranial neuropathies (57.1%). Electrodiagnostic studies were conducted in 3 with only one showing features consistent with a radicular process. Serum and CSF angiotensin-converting enzyme levels were elevated in 38.5% and 0.0%, respectively. CSF white blood cell and protein were elevated in 92.9%. Corticosteroids were tried in all patients with durable stabilization or improvement in only 3 (21.4%). Second-line agents associated with improvement included methotrexate/infliximab (3/4, 75%), methotrexate (3/4, 75.0%), and azathioprine (1/1, 100%). During a median follow-up of 22.5 months, the final median mRS score was 3. Relapses occurred at a median of 6 months in 21.4%. In 9 patients with MRI follow-up, 6 improved (66.7%), 1 stabilized (11.1%), and 2 worsened (22.2%).

DISCUSSION

Characteristic features of cauda equina involvement by neurosarcoidosis include chronically delayed presentations, nodular enhancement on MRI, poor response to corticosteroids, and substantial resultant neurologic disability.

摘要

背景与目的

结节病是一种多系统肉芽肿性疾病,3%-5%的病例会影响神经系统。它几乎可以影响神经系统的任何部位。马尾神经受累是一种研究较少的表型,关于其自然病史和最佳治疗方法仍存在疑问。本研究旨在研究影响马尾神经的神经结节病的长期临床演变、治疗反应以及临床和影像学结果。

方法

回顾性评估 2011 年 1 月 1 日至 2021 年 12 月 8 日期间在埃默里大学接受治疗的神经结节病患者,以确定马尾神经疾病的表现,并纳入可以通过 MRI 或肌电图证实马尾神经受累的患者。

结果

在 216 例患者中,14 例(6.5%)涉及马尾神经。中位年龄为 49.5 岁,大多数为女性(85.7%)和非裔美国人(64.3%)。慢性(>28 天)表现最为常见(78.6%),但也有急性(<7 天,14.3%)和亚急性(7-28 天,7.1%)表现。最低点的改良 Rankin 量表(mRS)评分中位数为 3 分(范围 2-4)。症状呈不对称性,占 78.6%,包括腿部麻木(85.7%)、腿部无力(64.3%)、会阴麻木(35.7%)、疼痛(42.3%)和失禁(21.4%)。MRI 显示马尾神经增强 100%,结节样表现 78.6%,弥漫性受累 71.4%。同时存在脊髓炎很常见(颈段 28.6%、胸段 35.7%和圆锥部 28.6%)。颅内炎症包括脑膜炎(71.4%)和颅神经病变(57.1%)。仅对 3 例患者进行了电诊断研究,其中只有 1 例显示出神经根病变的特征。血清和 CSF 血管紧张素转换酶水平分别升高 38.5%和 0.0%。CSF 白细胞和蛋白均升高 92.9%。所有患者均尝试使用皮质类固醇治疗,但只有 3 例(21.4%)稳定或改善。与改善相关的二线药物包括甲氨蝶呤/英夫利昔单抗(3/4,75%)、甲氨蝶呤(3/4,75.0%)和硫唑嘌呤(1/1,100%)。在中位随访 22.5 个月时,最终中位 mRS 评分为 3 分。21.4%的患者在 6 个月时复发。在 9 例接受 MRI 随访的患者中,6 例改善(66.7%),1 例稳定(11.1%),2 例恶化(22.2%)。

讨论

马尾神经受累的神经结节病的特征包括慢性延迟表现、MRI 上结节样增强、对皮质类固醇反应差和严重的神经功能障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ece0/9128042/4d1b3f2d07be/NEURIMMINFL2021039748f1.jpg

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