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巨大发育性静脉异常与急性播散性脑脊髓炎的关联:一例报告及磁共振灌注研究

Association of a giant developmental venous anomaly and acute disseminated encephalomyelitis: A case report and magnetic resonance perfusion study.

作者信息

Deprez Louis, Lommers Emilie

机构信息

Departement of Radiology, CHU de Liège, Belgium.

Department of Neurology, CHU de Liège, Belgium.

出版信息

Neuroradiol J. 2025 Jun 30:19714009251356989. doi: 10.1177/19714009251356989.

Abstract

We describe the first reported association between acute disseminated encephalomyelitis (ADEM) and giant developmental venous anomaly (DVA) in the context of myelin oligodendrocyte associated glycoprotein (MOG) associated disorder (MOGAD). Patient was a young woman presenting with headache, bradypsychia and tetrapyramidal syndrome. Imaging showed disseminated tumefactive inflammatory lesions in the brain and spinal cord, with a massive right frontal lobe lesion centred around a giant DVA. Demyelinating inflammatory lesions are known to occur in a perivenular pattern, and the association between some inflammatory diseases such as multiple sclerosis (MS) and DVA has already been described. Developmental venous anomalies are variant of the normal venous drainage of the brain, responsible of a local alteration of the venular network, and micro-perfusion anomalies as well as possible increased of blood-brain barrier permeability. As such, they might be responsible for a favourable environment for pathogenic auto-antibodies penetrance in such region, potentializing the inflammatory lesion size. Perfusion imaging showed a significant increase in regional blood volume and blood transit time in the DVA and the surrounding brain tissue, which regressed in the follow-up imaging studies after the acute stage. This case illustrates the potential role of DVA in the setting of demyelinating diseases, and its consequences on the local micro-perfusion of the brain, evolving between the acute and chronic phase of the illness.

摘要

我们描述了在髓鞘少突胶质细胞相关糖蛋白(MOG)相关疾病(MOGAD)背景下,首次报道的急性播散性脑脊髓炎(ADEM)与巨大发育性静脉异常(DVA)之间的关联。患者为一名年轻女性,表现为头痛、精神迟缓及锥体束征。影像学检查显示脑和脊髓存在散在的肿胀性炎性病变,其中一个巨大的右额叶病变以一个巨大的DVA为中心。已知脱髓鞘炎性病变呈血管周围分布,并且已经描述了一些炎性疾病如多发性硬化(MS)与DVA之间的关联。发育性静脉异常是脑正常静脉引流的变异,导致静脉网络局部改变、微灌注异常以及血脑屏障通透性可能增加。因此,它们可能为致病性自身抗体在该区域的穿透创造了有利环境,从而使炎性病变扩大。灌注成像显示DVA及其周围脑组织的局部血容量和血流通过时间显著增加,在急性期后的随访影像学研究中这些指标有所恢复。该病例说明了DVA在脱髓鞘疾病中的潜在作用及其对脑局部微灌注的影响,这种影响在疾病的急性期和慢性期之间演变。

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本文引用的文献

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