Cerebral Amyloid Angiopathy: A Case Report.

IF 1 Q3 MEDICINE, GENERAL & INTERNAL
Cureus Pub Date : 2025-05-28 eCollection Date: 2025-05-01 DOI:10.7759/cureus.84989
Fatima Alam, Anup Banerjee, Chaminda Jayawarna
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Abstract

Cerebral amyloid angiopathy (CAA) is a cerebrovascular condition characterized by the buildup of beta-amyloid protein within the walls of small and medium-sized blood vessels in the brain's cortex and leptomeninges. Clinically, it can present with a range of neurological symptoms, including recurrent headaches, cognitive disturbances, seizures, and focal deficits. A key feature of CAA is the tendency for lobar brain hemorrhages, though its clinical and radiological profile can overlap with other neurological disorders such as Alzheimer's disease, demyelinating conditions, vascular syndromes, and neoplasms. CAA pathology is frequently observed in individuals with Alzheimer's disease, with a subset showing significant vascular involvement. Although histopathological confirmation remains definitive, advanced imaging, particularly MRI, has become central to diagnosis, often identifying features such as cortical microbleeds, superficial siderosis, and non-deep (lobar) hemorrhages. In some presentations, especially inflammatory variants, patients may benefit from immunosuppressive treatment such as corticosteroids, making early diagnosis critical. Recognizing the distinction between CAA-related hemorrhages and other causes of cerebral bleeding is vital for timely and appropriate management. We present a case of an elderly male who had multiple hospital presentations with unexplained self-resolving expressive dysphasia, seizure, and gradually increasing confusion with the possibility of underlying dementia that responded well to high-dose steroids. This case underscores the need to consider inflammatory cerebral amyloid angiopathy (iCAA) as a differential in patients with recurrent, unexplained neurological symptoms with CT evidence of micro- and macro-hemorrhages and a dramatic response to steroids for symptomatic improvement. Improved awareness of atypical presentations and the utility of MRI can support earlier intervention. Further investigation is needed to refine diagnostic tools, identify reliable biomarkers, and explore therapeutic strategies targeting the underlying vascular and inflammatory mechanisms of the disease.

脑淀粉样血管病1例报告。
脑淀粉样血管病(CAA)是一种脑血管疾病,其特征是-淀粉样蛋白在大脑皮层和脑轻脑膜的中小血管壁内积聚。临床表现为一系列神经系统症状,包括复发性头痛、认知障碍、癫痫发作和局灶性缺陷。CAA的一个关键特征是有大叶性脑出血的倾向,尽管其临床和放射学特征可能与其他神经系统疾病如阿尔茨海默病、脱髓鞘疾病、血管综合征和肿瘤重叠。CAA病理在阿尔茨海默病患者中经常观察到,其中一个亚群表现出明显的血管受累。虽然组织病理学证实仍然是明确的,但先进的成像,特别是MRI,已经成为诊断的核心,通常可以识别诸如皮质微出血、浅表性铁沉着和非深部(大叶)出血等特征。在某些情况下,特别是炎症变异,患者可能受益于免疫抑制治疗,如皮质类固醇,这使得早期诊断至关重要。认识到caa相关出血与其他原因脑出血的区别对于及时和适当的治疗至关重要。我们报告了一例老年男性患者,他多次出现不明原因的自我解决的表达性吞咽障碍,癫痫发作,并逐渐增加对潜在痴呆可能性的混淆,对大剂量类固醇反应良好。本病例强调需要将炎症性脑淀粉样血管病(iCAA)作为复发性、无法解释的神经系统症状患者的鉴别指标,CT表现为微观和宏观出血,并对类固醇治疗症状改善有显著反应。提高对非典型表现的认识和MRI的应用可以支持早期干预。需要进一步的研究来完善诊断工具,确定可靠的生物标志物,并探索针对该疾病潜在血管和炎症机制的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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