多发性脑微梗死:脑淀粉样血管病相关炎症的罕见表现。

Aikaterini Theodorou, Athanasios Tsibonakis, Ioannis S Pateras, Georgia Kaloudi, Eleni Bakola, Maria Chondrogianni, Elissavet Andreadou, Ioannis G Panayiotides, Georgios Tsivgoulis
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引用次数: 0

摘要

背景:脑淀粉样血管病相关炎症(CAA-ri)是一种独特但罕见的CAA亚型。高分辨率磁共振成像(MRI)的可用性越来越高,目前可以增加对该实体的识别和诊断,而无需进行脑活检。然而,在具有典型临床特征但表现不常见的神经影像学发现的罕见病例中,为了早期可靠的诊断,需要进行脑活检。病例描述:一名71岁男性,因头痛、呕吐、定向障碍和意识受损1周而出现动脉高血压。脑MRI显示多发急性皮质/皮质下微梗死,少量微出血,广泛的右侧顶骨和左侧额颞薄脑膜增强。经过广泛的诊断检查,排除感染性、肿瘤性和自身免疫性病因后,患者进行了脑活检。组织学显示小动脉壁淀粉样蛋白沉积,患者符合可能的CAA-ri的诊断标准,并伴有病理支持。他接受静脉注射甲基强的松龙,随后口服类固醇逐渐减少,显示临床和放射学改善,钆增强完全消除。随访MRI显示脑微出血增加,患者符合CAA-ri神经影像学标准。结论:本病例强调了临床神经科医师持续警惕CAA-ri诊断的重要性,以及脑活检对急性微梗死等非典型神经影像学表现的CAA-ri患者的诊断价值。早期诊断和及时治疗可以改善这种罕见疾病的预后和病情的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Multiple cerebral microinfarcts: an uncommon presentation of Cerebral Amyloid Angiopathy-related inflammation.

Multiple cerebral microinfarcts: an uncommon presentation of Cerebral Amyloid Angiopathy-related inflammation.

Multiple cerebral microinfarcts: an uncommon presentation of Cerebral Amyloid Angiopathy-related inflammation.

Background: Cerebral Amyloid Angiopathy-related inflammation (CAA-ri) is a distinct but rare subset of CAA. The greater availability of high resolution Magnetic Resonance Imaging (MRI) has currently allowed the increasing recognition and diagnosis of this entity, without the risk of a brain biopsy. However, in rare cases with typical clinical characteristics but uncommon neuroimaging findings at presentation, the brain-biopsy is required for an early and reliable diagnosis.

Case description: A 71-year-old man with arterial hypertension presented due to 1-week history of headache, vomiting, disorientation and impaired consciousness. Brain MRI revealed multiple acute cortical/subcortical microinfarcts, scarce microbleeds, extensive right parietooccipital and left frontotemporal leptomeningeal enhancement. After an extensive diagnostic work-up, excluding infectious, neoplastic and autoimmune etiologies, the patient underwent brain-biopsy. Histology disclosed amyloid deposition in an arteriolar wall and the patient fulfilled diagnostic criteria for probable CAA-ri with supporting pathology. He received intravenous methylprednisolone, followed by oral tapering with steroids showing clinical and radiological improvement with complete resolution of gadolinium enhancement. Follow-up MRI revealed an increase of cerebral microbleeds and the patient fulfilled CAA-ri neuroimaging criteria.

Conclusions: This case highlights the importance of continuous vigilance from clinical neurologists to detect CAA-ri diagnosis and the diagnostic value of brain-biopsy in CAA-ri patients with atypical neuroimaging presentation, such as acute microinfarcts. The early diagnosis and the prompt treatment initiation can improve the prognosis and the evolution of this rare disorder.

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