1 Department of Neurology, China-Japan Friendship Hospital, Beijing, China.
2 Department of Rheumatology, China-Japan Friendship Hospital, Beijing, China.
Cell Transplant. 2019 Aug;28(8):1045-1052. doi: 10.1177/0963689719846838. Epub 2019 May 7.
It is important to investigate the clinical characteristics and identify the stroke mechanisms of patients with autoimmune disease-related stroke, which are necessary for early etiology diagnosis, accurate treatment and preventive strategies. In this article we retrospectively studied eight cases of acute ischemic stroke associated with autoimmune diseases, and without competing conventional stroke etiologies. The characteristics of stroke (clinical and radiological features), the laboratory tests especially serum D-dimer levels (as a marker of hypercoagulable state), and embolic signals on transcranial Doppler were evaluated for all eight patients. High-resolution magnetic resonance imaging (HRMRI), which can help to evaluate vasculitis was performed in four patients. The possible underlying mechanisms of these cases were discussed based on these manifestations. As a result, autoimmune diseases in our study included systemic lupus erythematosus (=5), mixed connective tissue disease (=1), central nervous system vasculitis (=1), and Takayasu arteritis (=1). All eight patients presented with acute infarction lesions in ≥2 vascular territories. Most patients presented with numerous small and medium infarction lesions located in the cortical and subcortical areas. Multiple stroke mechanisms were involved in these cases, including hypercoagulability (=4), cardiac embolism (=1) and vasculitis (=3). Embolic signals could be detected on transcranial Doppler in all three stroke mechanisms. In conclusion, our study revealed the characteristics of autoimmune disease-related stroke. For patients with multiple acute cerebral infarcts within non-single arterial territories, autoimmune disease is an important etiology not to be neglected. Multiple stroke mechanisms were involved in these cases.
研究自身免疫性疾病相关卒中患者的临床特征和明确其卒中机制非常重要,这对于早期病因诊断、准确治疗和预防策略至关重要。本文回顾性研究了 8 例无其他常见卒中病因的急性缺血性卒中合并自身免疫性疾病患者。我们评估了所有 8 例患者的卒中特征(临床和影像学特征)、实验室检查,尤其是血清 D-二聚体水平(作为高凝状态的标志物),以及经颅多普勒的栓子信号。4 例患者进行了高分辨率磁共振成像(HRMRI)检查,有助于评估血管炎。基于这些表现讨论了这些病例的潜在发病机制。研究中自身免疫性疾病包括系统性红斑狼疮(=5)、混合性结缔组织病(=1)、中枢神经系统血管炎(=1)和 Takayasu 动脉炎(=1)。8 例患者均表现为≥2 个血管区域的急性梗死病灶。大多数患者表现为皮质和皮质下区域存在多发小和中等大小梗死病灶。这些病例涉及多种卒中机制,包括高凝状态(=4)、心源性栓塞(=1)和血管炎(=3)。经颅多普勒可检测到所有 3 种卒中机制中的栓子信号。总之,本研究揭示了自身免疫性疾病相关卒中的特征。对于多个非单一动脉区域内发生急性多发性脑梗死的患者,自身免疫性疾病是一个不容忽视的重要病因。这些病例涉及多种卒中机制。