Ischemic Stroke with Antiphospholipid Syndrome in a Myotonic Dystrophy Type 1 Patient: A Rare Case Report

E. Lee, D. Shin, Y. Ko, S. Jun
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Abstract

Myotonic dystrophy type 1 (DM1) is a rare autosomal dominant disorder with various phenotypes involving multiple systems. Stroke co-occurrence in DM1 is rare, but can cause severe dysfunction in a patient’s quality of life. However, the mechanism of stroke in patients with DM1 is poorly understood. In this case report, we present a patient who was diagnosed with DM1 while suffering from a brain embolic infarction due to antiphospholipid syndrome (APS). This is the first known case of DM1 with APS. The coexistence of these two multisystem diseases may make the diagnosis difficult, and there is the possibility of symptoms involving multiple organs. We should pay attention to the possibility of the coexistence of autoimmune disease and stroke in DM1 patients based on this rare case of a DM1 patient with stroke and an autoimmune disease.
1型强直性肌营养不良患者缺血性卒中伴抗磷脂综合征:一例罕见病例报告
肌强直性营养不良1型(DM1)是一种罕见的常染色体显性遗传病,具有多种表型,涉及多个系统。在DM1中同时发生中风是罕见的,但会导致患者生活质量的严重功能障碍。然而,DM1患者发生脑卒中的机制尚不清楚。在这个病例报告中,我们提出了一个被诊断为DM1的患者,同时患有因抗磷脂综合征(APS)引起的脑栓塞性梗死。这是已知的首例DM1伴APS病例。这两种多系统疾病的共存可能使诊断变得困难,并且有可能出现累及多器官的症状。基于这一罕见的DM1患者卒中合并自身免疫性疾病的病例,我们应该注意DM1患者自身免疫性疾病和卒中共存的可能性。
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