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Iranian Heart Journal، جلد ۲۴، شماره ۲، صفحات ۱۱۴-۱۱۷
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عنوان انگلیسی Acute Aortic Dissection in a 35-year-old Woman With Turner Syndrome: A Case Report
چکیده انگلیسی مقاله Turner Syndrome occurs when one of the X chromosomes is missing, either partially or completely. Heart defects associated with some cases of Turner syndrome can increase the risk of severe, life-threatening complications, including pulmonary hypertension and aortic dissection. A 35-year-old woman, a known case of Turner syndrome, presented with acute dissection in the ascending aorta (Type A Stanford). The patient had a successful aortic valve repair surgery with a Dacron tube graft interposition. The risk of aortic dissection in Turner syndrome is 100 times greater than that in the general population. Diagnosis was made by transthoracic echocardiography and computed tomography angiography. Due to the small size of the femoral artery, cannulation was done in the innominate artery. Cardiopulmonary bypass was established, and systemic cooling was initiated to a temperature of 25 ℃. The patient was discharged from the hospital in good condition. (Iranian Heart Journal 2023; 24(2): 114-117)
کلیدواژه‌های انگلیسی مقاله Aortic dissection,Adult congenital heart disease,Bicuspid aortic valve,Turner syndrome,Type A Stanford
نویسندگان مقاله Hamid Hoseinikhah |
Department of Cardiac Surgery, Imam Reza Hospital, Mashhad University of Medical Sciences, Mashhad, IR Iran.

Mahmoud Hoseinzadeh Maleki |
Department of Cardiac Surgery, Imam Reza Hospital, Mashhad University of Medical Sciences, Mashhad, IR Iran.

Farhad Samadieh |
Department of Cardiac Surgery, Imam Reza Hospital, Mashhad University of Medical Sciences, Mashhad, IR Iran.

Aliasghar Moeinipour |
Department of Cardiac Surgery, Imam Reza Hospital, Mashhad University of Medical Sciences, Mashhad, IR Iran.

نشانی اینترنتی http://journal.iha.org.ir/article_169032_a7dbed73985d31a3a7802d36f6768c89.pdf
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