Kountouris Evaggelos, Potsis Thomas, Nikas Dimitrios, Siogas Konstantinos
Department of Cardiology, "G.Hatzikosta", General Hospital of Ioannina 45001 Ioannina Greece.
Cases J. 2009 Jun 15;2:6308. doi: 10.4076/1757-1626-2-6308.
Aortic coarctation is a congenital malformation of the aorta usually diagnosed and corrected early in life. Long-term survival is exceptional in patients with untreated aortic coarctation. In this case report, we present a late diagnosis of aortic coarctation in a 72-year-old female. Our patient was relatively asymptomatic until she presented with exertional dyspnea and fatigue in her seventh decade of life. The patient was managed conservatively with aggressive antihypertensive medication. After the 1-year follow-up visit, the patient was in good clinical condition, without, however, adequate control of blood pressure.
主动脉缩窄是一种主动脉先天性畸形,通常在生命早期被诊断并得到纠正。未经治疗的主动脉缩窄患者长期存活的情况极为罕见。在本病例报告中,我们呈现了一名72岁女性主动脉缩窄的晚期诊断情况。我们的患者在70岁之前相对无症状,直到出现劳力性呼吸困难和疲劳。该患者采用积极的抗高血压药物进行保守治疗。经过1年的随访,患者临床状况良好,然而血压并未得到充分控制。