Recurrent Cerebral Infarction Due to Moyamoya Disease Complicated With Systemic Lupus Erythematosus: A Case Report and Literature Review.

IF 1.1 4区 医学 Q4 CLINICAL NEUROLOGY Neurologist Pub Date : 2024-01-01 DOI:10.1097/NRL.0000000000000517
Qisong Wang, Qiang Yao, Si Yuan, Yan Shen, Yang Feng, Luji Liu, Yipu Zhu, Yanying Zhao, Junzhao Cui, Jin Qin, Jing Tian, Ruijie Zhao, Lijuan Liu, Yicong Zhou, Xiaoyun Liu
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Abstract

Introduction: We report a rare case of moyamoya disease caused by an RNF213 mutation, complicated with systemic lupus erythematosus.

Case report: A 32-year-old woman experienced 4 cerebral ischemia stroke events within 6 months. The main symptom was left limb weakness with blurred vision in the right eye. Results of digital subtraction angiography conducted at another hospital were consistent with moyamoya disease. On genetic testing, we found that the patient carried 2 mutations in the moyamoya disease-related gene RNF213 (p.R4810K, p.T1727M). On the basis of the laboratory immunologic indicators, such as positive antibodies and abnormal immunoglobulin levels and imaging examinations, the patient was finally diagnosed as moyamoya disease complicated with systemic lupus erythematosus. She was treated with aspirin, butylphthalide, urinary kallidinogenase, and sodium methylprednisolone.

Conclusions: This was a 32-year-old young patient diagnosed with moyamoya disease carrying RNF213 gene mutation and accompanied by lupus with cerebral ischemic event as the first occurrence. The patient's condition was complex; therefore, comprehensive analysis and in-depth consideration were needed to avoid a missed diagnosis and misdiagnosis. When the primary disease cannot be identified, genetic testing can help to clarify the diagnosis of moyamoya disease.

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系统性红斑狼疮并发莫亚莫亚病导致的复发性脑梗塞:病例报告与文献综述
导言:我们报告了一例罕见的由 RNF213 基因突变引起的莫亚莫亚病,并发系统性红斑狼疮:病例报告:一名 32 岁女性在 6 个月内经历了 4 次脑缺血中风。主要症状为左侧肢体无力,右眼视力模糊。在另一家医院进行的数字减影血管造影检查结果与 moyamoya 病一致。通过基因检测,我们发现患者携带两个与莫亚莫亚病相关的基因 RNF213 突变(p.R4810K 和 p.T1727M)。根据抗体阳性、免疫球蛋白水平异常等实验室免疫学指标和影像学检查,患者最终被诊断为莫亚莫亚病并发系统性红斑狼疮。她接受了阿司匹林、丁苯酞、尿凯利苷原酶和甲基强的松龙钠治疗:这是一名 32 岁的年轻患者,被诊断为携带 RNF213 基因突变的 moyamoya 病,并伴有狼疮,首次发生脑缺血事件。患者病情复杂,因此需要全面分析和深入考虑,以避免漏诊和误诊。当无法确定原发疾病时,基因检测有助于明确莫亚莫亚病的诊断。
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来源期刊
Neurologist
Neurologist 医学-临床神经学
CiteScore
1.90
自引率
0.00%
发文量
151
审稿时长
2 months
期刊介绍: The Neurologist publishes articles on topics of current interest to physicians treating patients with neurological diseases. The core of the journal is review articles focusing on clinically relevant issues. The journal also publishes case reports or case series which review the literature and put observations in perspective, as well as letters to the editor. Special features include the popular "10 Most Commonly Asked Questions" and the "Patient and Family Fact Sheet," a handy tear-out page that can be copied to hand out to patients and their caregivers.
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