Zafar Mansoor, Gajre Meera, Balagopal Aparna, Naqvi Syed Ashhar, Khalesi Darius S, Premathilaka Rusiru, Islam Ariful, Berliti Stefano, Hovagim Garabedyan, Hacikurt Kadir
Gastroenterology/General Internal Medicine, Royal Sussex County Hospital, University Hospitals Sussex National Health Service (NHS) Foundation Trust, Brighton, GBR.
General Internal Medicine, Conquest Hospital, St. Leonards-on-Sea, GBR.
Cureus. 2023 May 16;15(5):e39099. doi: 10.7759/cureus.39099. eCollection 2023 May.
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is a rare inherited disease that presents with neurologic manifestations such as stroke, psychiatric disturbances, migraine, and cognitive decline. We report a case of a previously well 27-year-old lady presenting with new onset confusion four weeks postpartum. On examination, there was right-sided weakness and tremors. A thorough history revealed existing diagnoses of CADASIL in 1 and 2-degree relatives. The diagnosis in this patient was confirmed by MRI of the brain and genetic testing for mutation. The patient was admitted to the stroke ward, treated with a single antiplatelet agent for stroke, and supported by speech and language therapy. There was a significant symptomatic improvement in her speech at the time of discharge. The mainstay of treatment for CADASIL remains symptomatic at this stage. This case report shows that the first presentation of CADASIL can mimic postpartum psychiatric disorders in a puerperal woman.
伴有皮质下梗死和白质脑病的常染色体显性遗传性脑动脉病(CADASIL)是一种罕见的遗传性疾病,表现为中风、精神障碍、偏头痛和认知衰退等神经学症状。我们报告一例病例,一名27岁既往健康的女性,产后四周出现新发意识模糊。检查发现右侧肢体无力和震颤。详细病史显示其一级和二级亲属中均有CADASIL确诊病例。该患者的诊断通过脑部MRI和基因突变检测得以证实。患者入住卒中病房,接受单一抗血小板药物治疗中风,并接受言语和语言治疗。出院时其言语症状有显著改善。现阶段CADASIL的主要治疗方法仍是对症治疗。本病例报告表明,CADASIL的首发症状在产褥期女性中可能类似产后精神障碍。