Tokue Masahide, Hara Hidehiko, Kurosawa Kenji, Nakamura Masato
Department of Cariovascular Medicine, Toho University Ohashi Medical Center, Tokyo, Japan.
Department of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
BMJ Case Rep. 2017 Sep 23;2017:bcr-2017-220786. doi: 10.1136/bcr-2017-220786.
Vascular Ehlers-Danlos Syndrome (vEDS) is a dominantly inherited connective tissue disorder characterised by colon rupture and arterial aneurysm, dissection and rupture. A patient was diagnosed with vEDS after a spontaneous colon rupture when he was brought to our institute because of sudden chest pain. An ECG revealed wide regional ST elevation, which was initially suggestive of acute myocarditis. On the second day, haemodynamics suddenly deteriorated because of a rapid accumulation of bloody pericardial effusion, and the patient died. Autopsy revealed an excessive spontaneous myocardial haemorrhage owing to fragility, which suggested an underlying disease-vEDS.
血管型埃勒斯-当洛综合征(vEDS)是一种常染色体显性遗传的结缔组织疾病,其特征为结肠破裂以及动脉动脉瘤、夹层形成和破裂。一名患者因突发胸痛被送至我院,在发生自发性结肠破裂后被诊断为vEDS。心电图显示广泛的ST段抬高,最初提示为急性心肌炎。第二天,由于血性心包积液迅速积聚,血流动力学突然恶化,患者死亡。尸检显示因血管脆性导致自发性心肌出血过多,提示潜在疾病——vEDS。