Brachial Artery Tear Occurring Concurrently with A Distal Biceps Injury Led to A Diagnosis of Ehlers-Danlos Syndrome Type IV

G. González, R. Dayal, Lee Andy, A. Golant
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Abstract

Ehlers-Danlos Syndrome (EDS) type IV is a connective tissue disorder with autosomal dominant inheritance. It can be potentially life-threatening due to increased risk of arterial rupture. The diagnosis is based on clinical findings including thin, translucent skin; bleeding propensity, rupture of vessels, and viscera. Isolated peripheral vascular injury may be the first presenting complaint, leading to eventual diagnosis in patients who often experience minimal trauma. We present a case of a brachial artery rupture requiring surgical reconstruction, eventually leading to the diagnosis of EDS type IV after a non-contact, low-energy injury to the arm of an adolescent.
肱动脉撕裂同时发生二头肌远端损伤导致诊断为Ehlers-Danlos综合征IV型
埃勒斯-丹洛斯综合征(EDS)IV型是一种常染色体显性遗传的结缔组织疾病。由于动脉破裂的风险增加,它可能会危及生命。诊断是基于临床发现,包括薄,半透明的皮肤;出血倾向、血管破裂和内脏。孤立的外周血管损伤可能是首次出现的主诉,最终诊断为创伤最小的患者。我们报告了一例需要手术重建的肱动脉破裂病例,最终诊断为青少年手臂非接触性低能量损伤后的EDS IV型。
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