戴克-戴维多夫-马森综合征非典型表现的病例报告。
A case report on atypical presentations of Dyke-Davidoff-Masson syndrome.
作者信息
Yang Bingjie, Hu Shuqi, Jiang Yiru, Shu Song, Zhou Huixia, Zhu Jiahui, Zhang Hao
机构信息
Department of Neurology, The Fourth School of Clinical Medicine, Zhejiang Chinese Medical University, Hangzhou First People's Hospital, Hangzhou, Zhejiang, China.
Department of Neurology, Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University, Hangzhou, Zhejiang, China.
出版信息
Heliyon. 2024 Aug 2;10(15):e35600. doi: 10.1016/j.heliyon.2024.e35600. eCollection 2024 Aug 15.
Dyke-Davidoff-Masson Syndrome (DDMS) is a rare neurological disease with an unknown incidence. The manifestations of DDMS are variable, while typical symptoms are seizures, hemiparesis, and mental retardation. Here, we present a case involving a 19-year-old male patient who presents with headaches, mood changes, and a history of seizures during childhood. Based on the neuroimages, a diagnosis of DDMS was established. The application of sertraline hydrochloride as a therapeutic intervention has alleviated the symptoms. This case report illustrates the importance of understanding the clinical features of DDMS based on imaging.
戴克-戴维多夫-马森综合征（DDMS）是一种发病率未知的罕见神经系统疾病。DDMS的表现多种多样，典型症状为癫痫发作、偏瘫和智力发育迟缓。在此，我们报告一例19岁男性患者，其表现为头痛、情绪变化，且有儿童期癫痫发作史。根据神经影像检查结果，确诊为DDMS。应用盐酸舍曲林作为治疗干预措施后症状有所缓解。本病例报告说明了基于影像学了解DDMS临床特征的重要性。
Zotero 插件