Unit of Neurology and Neurometabolic Disorders, Clinical Department of Neurological and Motor Sciences & University Department of Medicine, Surgery and Neuroscience, Azienda ospedaliero-universitaria Senese & University of Siena, "Santa Maria alle Scotte" NHS & University Hospital, 53100, Siena, Tuscany, Italy.
Unit of Anesthesiology, Emergency-Urgency Intensive Care and Transplants, Clinical Department of Emergency-Urgency and Transplants, Azienda Ospedaliero-universitaria Senese, "Santa Maria alle Scotte" NHS & University Hospital, 53100, Siena, Tuscany, Italy.
Neurol Sci. 2022 Nov;43(11):6381-6387. doi: 10.1007/s10072-022-06299-y. Epub 2022 Aug 5.
Cerebral amyloid angiopathy-related inflammation (CAA-ri) is a rare potentially reversible encephalopathy associated with an autoimmune process against proteins deposited in the walls of cortical and leptomeningeal brain vessels. Definite diagnosis requires histopathological features of vascular inflammation and amyloid deposition from brain biopsy. Clinical-neuroradiological criteria have been recently introduced and validated to reduce the need for biopsy. The purpose of this paper is to report a historical retrospective review of clinical-neuroradiological follow-up of two patients with probable CAA-ri and five patients with a reasonably probable suspect of CAA-ri (4 females, 3 males, patient's age at admission: 66-79 years) seen at our institution between 2007 and 2021, focusing on clinical and neuroradiological awareness to this entity and variable response to immunotherapy.
Clinical features at presentation included subacute to acute confusion (6/7), seizures (4/7), cognitive impairment (5/7), and focal neurological signs (3/7). Neuroradiology included braincomputed tomography followed by magnetic resonance imaging. Infectious diseases and autoimmune workups were then performed.
CSF analysis was performed in two patients. Cerebral angiography was performed in two patients, to rule out vascular malformations. Hemorrhagic posterior reversible encephalopathy syndrome has been suspected in two patients. Four patients underwent immunotherapy with corticosteroids followed by reduction of brain dysfunctions. Three patients did not undergo immunotherapy but underwent clinical and/or neuroradiological remission.
Patients with CAA-ri present a rare steroid-responsive acute to subacute brain dysfunction. Thus, it has to be known and recognized both clinically and neuroradiologically. Spontaneous clinical and/or neuroradiological improvement is possible in patients with mild symptoms.
脑淀粉样血管病相关炎症(CAA-ri)是一种罕见的潜在可逆转的脑病,与针对沉积在皮质和软脑膜脑血管壁上的蛋白质的自身免疫过程有关。明确诊断需要从脑活检中获得血管炎症和淀粉样沉积的组织病理学特征。最近已经引入并验证了临床神经放射学标准,以减少对活检的需求。本文的目的是报告我们机构在 2007 年至 2021 年间治疗的两名可能的 CAA-ri 患者和五名合理怀疑的 CAA-ri 患者(4 名女性,3 名男性,入院时患者年龄:66-79 岁)的临床神经放射学随访的历史回顾性研究,重点是对这种疾病的临床和神经放射学认识以及免疫治疗的可变反应。
发病时的临床特征包括亚急性至急性意识混乱(6/7)、癫痫发作(4/7)、认知障碍(5/7)和局灶性神经体征(3/7)。神经影像学包括脑计算机断层扫描(CT),随后是磁共振成像(MRI)。然后进行了传染病和自身免疫检查。
对两名患者进行了脑脊液分析。对两名患者进行了脑血管造影,以排除血管畸形。两名患者疑似患有出血性后部可逆性脑病综合征。四名患者接受了皮质类固醇免疫治疗,随后脑功能障碍得到改善。三名患者未接受免疫治疗,但出现了临床和/或神经放射学缓解。
CAA-ri 患者表现为罕见的类固醇反应性急性至亚急性脑功能障碍。因此,无论是在临床上还是在神经放射学上,都必须了解并认识到这一点。对于症状较轻的患者,可能会出现自发的临床和/或神经放射学改善。