Renal Infarction in Vascular Ehlers-Danlos Syndrome

Hea Ran Lee, Si Chan Kim, E. Yang, Susanne Jung, J. Chang, Eun Kyoung Lee
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Abstract

Renal infarction is a condition caused by sudden disturbance of renal arterial blood flow, which occurs frequently in cardioembolic disease, renal artery injury (trauma, Marfan syndrome, rarely Ehlers-Danlos syndrome), and in association with a hypercoagulable state. Ehlers-Danlos syndrome is a rare hereditary connective tissue disease characterized by skin fragility, hyperelasticity, hypermobility of small joints, and easy bruising. Among the subtypes, vascular Ehlers-Danlos syndrome is a very rare genetic disease caused by a mutation in the COL3A1 gene. As blood vessels are fragile due dysfunctional collagen synthesis, complications of bleeding due to arterial dissection or rupture are common in patients with this disease. Here, we report a case of vascular Ehlers-Danlos syndrome diagnosed based on a renal infarction caused by thrombus and renal artery injury; we also present a review of the relevant literature.
血管性埃勒-丹洛斯综合征的肾梗死
肾梗死是一种由肾动脉血流突然紊乱引起的疾病,常见于心栓塞性疾病、肾动脉损伤(外伤、马凡氏综合征,很少见于埃勒-丹洛斯综合征),并与高凝状态有关。ehers - danlos综合征是一种罕见的遗传性结缔组织疾病,其特征是皮肤脆弱、超弹性、小关节过度活动和容易挫伤。在这些亚型中,血管性埃勒斯-丹洛斯综合征是一种由COL3A1基因突变引起的非常罕见的遗传性疾病。由于胶原合成功能障碍导致血管脆弱,动脉剥离或破裂导致出血是本病患者常见的并发症。在此,我们报告一例血管性埃勒-丹洛斯综合征,诊断基于血栓和肾动脉损伤引起的肾梗死;我们还对相关文献进行了综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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