可能的脑淀粉样血管病相关炎症伴自发缓解。罕见疾病的罕见表现。

IF 0.6 Q4 CLINICAL NEUROLOGY
Francisco Caiza-Zambrano, Luis Ariel Miquelini, Fabio Gonzalez, Julio Galarza, Mauricio Benetti, Yemina Neme-Segura, Patxi Zavala-Gottau, Carlos Rugilo, Claudia Uribe-Roca, Manuel Fernández-Pardal, Luciana León-Cejas, Ricardo Reisin, Pablo Bonardo
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引用次数: 0

摘要

脑淀粉样血管病相关炎症(CAA-ri)是一种罕见的疾病,由血管周围β-淀粉样蛋白沉积引起的炎症反应引起。CAA-ri在少数病例中被描述为自发缓解。我们报告一位76岁的男性,他表现为头痛和意识不清。体格检查未发现神经功能障碍。脑MRI显示不对称白质高信号伴小脑膜增强和多处皮质微出血,与可能的CAA-ri相符。一个月后,脑MRI显示白质异常完全消失,无需治疗。本病例提示CAA-ri的病程可能具有自限性。此外,我们对以前报告的病例进行了审查。这使得医生知道这个实体,适当地排除鉴别诊断,并在影像学检查中识别结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Probable Cerebral Amyloid Angiopathy-Related Inflammation With Spontaneous Remission. A Rare Presentation of a Rare Disease.

Cerebral Amyloid Angiopathy-related inflammation (CAA-ri) is a rare condition caused by an inflammatory response against perivascular β-amyloid deposits. CAA-ri with spontaneous remission has been described in a few cases. We report a 76-year-old man who presented with headache and confusion. No neurological deficit was evidenced on physical examination. Brain MRI showed asymmetric white matter hyperintensities with leptomeningeal enhancement and multiple cortical microbleeds, compatible with probable CAA-ri. One month later, brain MRI showed complete resolution of the white matter abnormalities without treatment. This case suggests that the course of CAA-ri may be self-limited. Furthermore, we conducted a review of previously reported cases. This allows physicians to know this entity, properly rule out differential diagnoses, and recognize findings in imaging studies.

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来源期刊
Neurohospitalist
Neurohospitalist CLINICAL NEUROLOGY-
CiteScore
1.60
自引率
0.00%
发文量
108
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