Hagouch Amal, Rouillon Natacha, Kabbadj Aysha, Proulx-Chartier Léa, Parenteau Ève, Li Jimmy, Bocti Christian, Toffa Dènahin Hinnoutondji
Neurology Division, Université de Sherbrooke Health Centre (CHUS), Sherbrooke, QC, Canada.
Department of Psychiatry, Université de Montreal, Montreal, QC, Canada.
J Geriatr Psychiatry Neurol. 2025 Apr 28;38(6):8919887251338270. doi: 10.1177/08919887251338270.
ObjectiveMirrored self-misidentification syndrome (MSMS) is a rare form of delusional misidentification syndrome characterized by the inability to recognize one's own reflection. We conducted a systematic review aiming to describe the epidemiology, clinical presentation, and management of individuals with MSMS.MethodsA comprehensive literature search was performed using original case reports/series on patients with MSMS. Univariate analyses were performed to assess patient demographics, clinical, paraclinical, and treatment-related characteristics. The methodological quality of included articles was evaluated using a standardized tool.ResultsOf 76 articles screened, 28 were included, with 36 patients analyzed. Median age was 77.0 (interquartile range: 72.0, 80.0) years; most patients were female (60.7%). Over half of the cases had a diagnosis of dementia, mostly Alzheimer's disease (50.0%), Lewy Body Disease (20.0%), and vascular dementia (10.0%), while the other diagnosis included stroke (3.3%), schizophrenia (3.3%), schizoaffective disorder (3.3%), and rabies (3.3%). Initial clinical manifestations included psychiatric symptoms (66.7%) and cognitive decline (70.0%). Brain magnetic resonance (MRI) was reported in 31 cases, with 14 cases (45.1%) showing right hemisphere dysfunction. Pharmacological interventions were effective for twelve cases (48.0%), and non-pharmacological interventions such as covering mirror were effective for 8 cases (32.0%). Most included articles (64.3%) were evaluated to be at low risk of bias.ConclusionsMSMS are rare conditions that mostly present in patients with dementia. Despite the varied clinical presentations, frontal and right hemisphere dysfunctions appear to play a role in the pathophysiology of MSMS, adding to the evidence supporting "a neuroanatomy of the self" in the non-dominant hemisphere.
目的
镜像自我识别障碍综合征(MSMS)是一种罕见的妄想性识别障碍综合征,其特征是无法识别自己的镜像。我们进行了一项系统综述,旨在描述MSMS患者的流行病学、临床表现及管理方法。
方法
使用关于MSMS患者的原始病例报告/系列进行全面的文献检索。进行单因素分析以评估患者的人口统计学、临床、辅助检查及治疗相关特征。使用标准化工具评估纳入文章的方法学质量。
结果
在筛选的76篇文章中,纳入28篇,分析了36例患者。中位年龄为77.0(四分位间距:72.0,80.0)岁;大多数患者为女性(60.7%)。超过半数病例诊断为痴呆,主要是阿尔茨海默病(50.0%)、路易体病(20.0%)和血管性痴呆(10.0%),其他诊断包括中风(3.3%)、精神分裂症(3.3%)、分裂情感性障碍(3.3%)和狂犬病(3.3%)。初始临床表现包括精神症状(66.7%)和认知功能下降(70.0%)。31例患者报告了脑磁共振成像(MRI),14例(45.1%)显示右半球功能障碍。药物干预对12例患者有效(48.0%),非药物干预如遮盖镜子对8例患者有效(32.0%)。大多数纳入文章(64.3%)被评估为偏倚风险低。
结论
MSMS是罕见疾病,主要见于痴呆患者。尽管临床表现多样,但额叶和右半球功能障碍似乎在MSMS的病理生理过程中起作用,这进一步支持了非优势半球中“自我神经解剖学”的证据。