Thompson Norris B, Hamidian Jahromi Alireza, Ballard David H, Rao Vyas R, Samra Navdeep S
School of Medicine, Louisiana State University Health-Shreveport, Shreveport, LA.
Department of Surgery, Louisiana State University Health-Shreveport, Shreveport, LA.
Ann Vasc Surg. 2015;29(4):838.e11-5. doi: 10.1016/j.avsg.2014.11.016. Epub 2015 Feb 12.
Acquired coarctation of the thoracic aorta is a rare phenomenon in adults. The etiology is often idiopathic, but severe stenosis can develop from prior surgery, blunt thoracic aortic injuries, or severe atherosclerotic/atheroembolic disease. Common symptomatic presentations include refractory upper extremity hypertension and new-onset congestive heart failure. We present the case of a 52-year-old man who developed acquired thoracic aortic coarctation 30 years after a blunt trauma and deceleration injuries to the aorta requiring open surgical aortic repair. He presented with poorly controlled hypertension and new-onset heart failure and was treated surgically with endovascular repair.
获得性胸主动脉缩窄在成年人中是一种罕见现象。病因通常为特发性,但严重狭窄可由既往手术、钝性胸主动脉损伤或严重的动脉粥样硬化/动脉粥样栓塞性疾病发展而来。常见的症状表现包括难治性上肢高血压和新发充血性心力衰竭。我们报告一例52岁男性病例,该患者在主动脉钝性创伤和减速损伤30年后发生获得性胸主动脉缩窄,需要进行开放性主动脉手术修复。他表现为血压控制不佳和新发心力衰竭,接受了血管内修复手术治疗。