این سایت در حال حاضر پشتیبانی نمی شود و امکان دارد داده های نشریات بروز نباشند
Journal of Cardio-Thoracic Medicine، جلد ۱۲، شماره ۴، صفحات ۱۴۳۵-۱۴۳۸

عنوان فارسی
چکیده فارسی مقاله
کلیدواژه‌های فارسی مقاله

عنوان انگلیسی Ochronotic Heart Disease: A Case Report of Aortic Valve Replacement and Coronary Artery Bypass Grafting in a Patient with Alkaptonuria
چکیده انگلیسی مقاله Introduction: Alkaptonuria is an autosomal recessive genetic disorder that disrupts tyrosine metabolism, causing the buildup of homogentisic acid and its oxidized derivatives in tissues, including the heart, leading to potential health issues. Understanding Alkaptonuria pathophysiology and clinical manifestations is crucial for early recognition and appropriate management.Case Report: A 53-year-old man with severe aortic stenosis (AS) and coronary artery disease is scheduled for coronary artery bypass grafting (CABG) and aortic valve replacement (AVR) surgery. After median sternotomy and cardiopulmonary bypass, the aortotomy showed black discoloration of the aortic wall and valve.Conclusion: The patient's echocardiogram indicated very severe AS with thickened and calcified leaflets, moderate aortic regurgitation (AR), and mild mitral regurgitation (MR). The aortotomy revealed significant black discoloration of the aortic wall and valve, indicating a critical issue that demands immediate attention. These findings underscore the necessity for thorough preoperative assessment and careful perioperative management to improve outcomes.
کلیدواژه‌های انگلیسی مقاله Alkaptonuria, Coronary artery, Ochronotic

نویسندگان مقاله | Mahdi Kahrom
Department of Cardiovascular Surgery, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.


| Masoomeh Tabari
Department of Anesthesiology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.


| Shiva Rezaeian Deloei
Department of Anesthesiology, Mashhad University of Medical Sciences, Mashhad, Iran.


| Elham Shaarbaf Eidgahi
Department of Internal Medicine, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.



نشانی اینترنتی https://jctm.mums.ac.ir/article_25446.html
فایل مقاله فایلی برای مقاله ذخیره نشده است
کد مقاله (doi)
زبان مقاله منتشر شده en
موضوعات مقاله منتشر شده
نوع مقاله منتشر شده Case Report
برگشت به: صفحه اول پایگاه   |   نسخه مرتبط   |   نشریه مرتبط   |   فهرست نشریات