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酷似多发性硬化的大脑常染色体显性动脉病伴皮质下梗死和白质脑病:临床及磁共振成像警示征象的重要性

CADASIL mimicking multiple sclerosis: The importance of clinical and MRI red flags.

作者信息

Joshi Stuti, Yau Wayne, Kermode Allan

机构信息

Department of Neurology, Sir Charles Gairdner Hospital, Perth, Australia.

Department of Neurology, Sir Charles Gairdner Hospital, Perth, Australia.

出版信息

J Clin Neurosci. 2017 Jan;35:75-77. doi: 10.1016/j.jocn.2016.09.025. Epub 2016 Oct 20.

DOI:10.1016/j.jocn.2016.09.025
PMID:27773545
Abstract

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited small vessel disease, manifesting as recurrent ischaemic events, migraine with aura, behavioural disturbance and cognitive decline. We report two patients with CADASIL masquerading as multiple sclerosis (MS). A 23year old female presented with a visual scotoma and was discovered to have a corresponding retinal cotton wool spot. MRI brain revealed diffuse T2 hyperintensities suggestive of demyelination. A 56year old male presented with transient sequential paraesthesia, initially of the perineum followed by the right leg. He also reported memory and mood impairment with a history of migraine with aura. MRI of the brain showed diffuse bilateral white matter lesions with sparing of the anterior temporal poles. Both patients satisfied the modified McDonald diagnostic criteria and were initially thought to have MS. However, they did not satisfy the caveat of "no better explanation" and on subsequent testing NOTCH 3 mutations were identified in both patients [1]. These cases highlight the importance of careful clinical assessment and neuroimaging findings in identifying clinical and paraclinical 'red-flags' for a diagnosis other than MS.

摘要

伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)是一种遗传性小血管疾病,表现为反复发作的缺血性事件、伴先兆的偏头痛、行为障碍和认知衰退。我们报告了两名伪装成多发性硬化症(MS)的CADASIL患者。一名23岁女性出现视觉暗点,发现有相应的视网膜棉絮斑。脑部MRI显示弥漫性T2高信号,提示脱髓鞘。一名56岁男性出现短暂的顺序性感觉异常,最初是会阴部,随后是右腿。他还报告有记忆和情绪障碍,有伴先兆的偏头痛病史。脑部MRI显示双侧弥漫性白质病变,前颞极未受累。两名患者均符合修订的麦克唐纳诊断标准,最初被认为患有MS。然而,他们不符合“无更好解释”这一条件,后续检测发现两名患者均存在NOTCH 3突变[1]。这些病例凸显了在识别除MS以外诊断的临床和辅助临床“警示信号”时,仔细的临床评估和神经影像学检查结果的重要性。

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CADASIL mimicking multiple sclerosis: The importance of clinical and MRI red flags.酷似多发性硬化的大脑常染色体显性动脉病伴皮质下梗死和白质脑病:临床及磁共振成像警示征象的重要性
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CADASIL can mimic multiple sclerosis.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)可模仿多发性硬化症。
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[Differential diagnosis of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].[伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病的鉴别诊断]
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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)
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引用本文的文献

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Cereb Circ Cogn Behav. 2021 Feb 16;2:100006. doi: 10.1016/j.cccb.2021.100006. eCollection 2021.
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A Case of Atypical Multiple Sclerosis Mimicking Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Syndrome.一例酷似伴有皮质下梗死和白质脑病综合征的大脑常染色体显性动脉病的非典型多发性硬化病例。
Cureus. 2021 Jan 5;13(1):e12508. doi: 10.7759/cureus.12508.
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Periventricular Hyperintensities Mimicking Multiple Sclerosis.
模仿多发性硬化症的脑室周围高信号
Cureus. 2019 Aug 5;11(8):e5326. doi: 10.7759/cureus.5326.
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An Autopsy Proven Case of CSF1R-mutant Adult-onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (ALSP) with Premature Ovarian Failure.一例经尸检证实的伴有轴突球状体和色素性神经胶质细胞的CSF1R突变型成人起病白质脑病(ALSP)合并卵巢早衰病例。
Exp Neurobiol. 2019 Feb;28(1):119-129. doi: 10.5607/en.2019.28.1.119. Epub 2019 Feb 28.
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CADASIL: Treatment and Management Options.伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL):治疗与管理选择
Curr Treat Options Neurol. 2017 Sep;19(9):31. doi: 10.1007/s11940-017-0468-z.
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Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and management aspects.以大脑常染色体显性遗传性动脉病伴皮质下梗死和白质脑病(CADASIL)为例的小血管病:临床、诊断及管理方面的最新进展
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