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Article Dans Une Revue Journal of Stroke and Cerebrovascular Diseases Année : 2017

Radiologically Isolated Cerebral Amyloid Angiopathy-Related Inflammation

Résumé

In amyloid β-related angiitis of the central nervous system (also called cerebral amyloid angiopathy-related inflammation), cerebral amyloid angiopathy occurs in association with primary vasculitis of small- and medium-sized leptomeningeal and cortical arteries. To avoid brain biopsy, clinicoradiological criteria (including clinical features due to inflammation-related uni/multifocal white matter hyperintensities) for the diagnosis of cerebral amyloid angiopathy-related inflammation have been validated recently. We report 3 cases with acute symptoms directly related to cerebral amyloid angiopathy in the presence of asymptomatic cerebral amyloid angiopathy-related inflammation hyperintensities on initial magnetic resonance imaging. Recognizing radiological features of cerebral amyloid angiopathy-related inflammation in patients with cerebral amyloid angiopathy is important because radiological isolated cerebral amyloid angiopathy-related inflammation may become symptomatic and immunosuppressive treatment is often effective in cerebral amyloid angiopathy-related inflammation, although optimal treatment regimen is yet unknown. In contrast, apart from hypertension treatment, few therapeutic options exist in cerebral amyloid angiopathy.
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Dates et versions

hal-01892266 , version 1 (10-10-2018)

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Dimitri Renard, Anne Wacongne, Eric Thouvenot. Radiologically Isolated Cerebral Amyloid Angiopathy-Related Inflammation. Journal of Stroke and Cerebrovascular Diseases, 2017, 26 (11), pp.e218 - e220. ⟨10.1016/j.jstrokecerebrovasdis.2017.08.002⟩. ⟨hal-01892266⟩
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