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CLIPPERS 及其模拟物:新的 CLIPPERS 诊断标准的评估。

CLIPPERS and its mimics: evaluation of new criteria for the diagnosis of CLIPPERS.

机构信息

Department of Neurology, University Hospital of Montpellier, Montpellier, France

Centre d'Esclerosi Mútiple de Catalunya, Hospital Universitari Vall d'Hebron, Barcelona, Spain.

出版信息

J Neurol Neurosurg Psychiatry. 2019 Sep;90(9):1027-1038. doi: 10.1136/jnnp-2018-318957. Epub 2019 May 9.

Abstract

OBJECTIVE

To evaluate the accuracy of the recently proposed diagnostic criteria for chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS).

METHODS

We enrolled 42 patients with hindbrain punctate and/or linear enhancements (<3 mm in diameter) and tested the CLIPPERS criteria.

RESULTS

After a median follow-up of 50 months (IQR 25-82), 13 out of 42 patients were CLIPPERS-mimics: systemic and central nervous system lymphomas (n=7), primary central nervous system angiitis (n=4) and autoimmune gliopathies (n=2). The sensitivity and specificity of the CLIPPERS criteria were 93% and 69%, respectively. Nodular enhancement ( ≥ 3 mm in diameter), considered as a red flag in CLIPPERS criteria, was present in 4 out of 13 CLIPPERS-mimics but also in 2 out of 29 patients with CLIPPERS, explaining the lack of sensitivity. Four out of 13 CLIPPERS-mimics who initially met the CLIPPERS criteria displayed red flags at the second attack with a median time of 5.5 months (min 3, max 18), explaining the lack of specificity. One of these four patients had antimyelin oligodendrocyte glycoprotein antibodies, and the three remaining patients relapsed despite a daily dose of prednisone/prednisolone ≥ 30 mg and a biopsy targeting atypical enhancing lesions revealed a lymphoma.

CONCLUSIONS

Our study highlights that (1) nodular enhancement should be considered more as an unusual finding than a red flag excluding the diagnosis of CLIPPERS; (2) red flags may occur up to 18 months after disease onset; (3) as opposed to CLIPPERS-mimics, no relapse occurs when the daily dose of prednisone/prednisolone is ≥ 30 mg; and (4) brain biopsy should target an atypical enhancing lesion when non-invasive investigations remain inconclusive.

摘要

目的

评估最近提出的慢性淋巴细胞性炎症伴桥脑血管周围强化对类固醇反应性(CLIPPERS)的诊断标准的准确性。

方法

我们纳入了 42 例具有后颅窝点状和/或线状强化(直径<3mm)的患者,并对 CLIPPERS 标准进行了测试。

结果

在中位随访 50 个月(IQR 25-82)后,42 例患者中有 13 例为 CLIPPERS 模拟患者:系统性和中枢神经系统淋巴瘤(n=7)、原发性中枢神经系统血管炎(n=4)和自身免疫性神经病变(n=2)。CLIPPERS 标准的敏感性和特异性分别为 93%和 69%。结节性强化(直径≥3mm)被认为是 CLIPPERS 标准中的一个“红旗”,在 13 例 CLIPPERS 模拟患者中出现了 4 例,但在 29 例 CLIPPERS 患者中也出现了 2 例,这解释了其敏感性不足。在最初符合 CLIPPERS 标准的 13 例 CLIPPERS 模拟患者中,有 4 例在第二次发病时出现了“红旗”,中位时间为 5.5 个月(min 3,max 18),这解释了其特异性不足。这 4 例患者中有 1 例存在抗髓鞘少突胶质细胞糖蛋白抗体,其余 3 例患者尽管泼尼松/强的松的日剂量≥30mg,且针对非典型强化病变的活检显示为淋巴瘤,但仍出现复发。

结论

我们的研究表明:(1)结节性强化应更多地被视为一种不常见的表现,而非排除 CLIPPERS 诊断的“红旗”;(2)“红旗”可能在发病后 18 个月内出现;(3)与 CLIPPERS 模拟患者不同,当泼尼松/强的松的日剂量≥30mg 时,不会出现复发;(4)当非侵入性检查仍不确定时,脑活检应针对非典型强化病变。

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