Ilica Ahmet Turan, Bilici Aslan, Ilhan Abdullah, Kara Muammer, Gür Serkan
Diyarbakir, 21100, Turkey.
Int J Cardiovasc Imaging. 2007 Oct;23(5):645-8. doi: 10.1007/s10554-006-9135-2. Epub 2006 Oct 11.
Atypical coarctation of the descending thoracic and abdominal aorta is a very uncommon vascular disease. Congenital, acquired, inflammatory, and infectious etiologies have been proposed. Patients typically presents with uncontrolled secondary hypertension in the upper half of the body or hypotension in the lower extremities in the first three decades of their lives. We report the case of a 20-year-old man with severe hypertension. Diffuse coarctation of thoracoabdominal aorta associated with bilateral renal artery stenosis was demonstrated clearly by multidetector CT angiography. This is the first case of atypical aortic coarctation diagnosed by MDCTA.
非典型性胸降主动脉和腹主动脉缩窄是一种非常罕见的血管疾病。病因包括先天性、后天性、炎症性和感染性。患者通常在生命的头三十年出现上身难以控制的继发性高血压或下肢低血压。我们报告了一例20岁重度高血压男性患者。多层螺旋CT血管造影清晰显示了胸腹部主动脉弥漫性缩窄并伴有双侧肾动脉狭窄。这是首例通过多层螺旋CT血管造影诊断的非典型主动脉缩窄病例。