Aortic Dissection and Postpartum Cardiomyopathy in a Postpartum Young Woman: A Case Report Study
Author(s) -
R Jalalian,
Mehrdad Saravi,
Bahar Banasaz
Publication year - 2014
Publication title -
iranian red crescent medical journal
Language(s) - English
Resource type - Journals
eISSN - 2074-1812
pISSN - 2074-1804
DOI - 10.5812/ircmj.9849
Subject(s) - medicine , aortic dissection , peripartum cardiomyopathy , chest pain , abdominal pain , dissection (medical) , cardiomyopathy , respiratory distress , surgery , pregnancy , aorta , postpartum period , abdominal aorta , cardiology , heart failure , biology , genetics
Aortic dissection is a rare condition in young women and usually related with congenital anomalies of aorta and connective tissue disorders. We reported a 34-year-old postpartum woman with aortic dissection. Case Presentation: The patient complained of respiratory distress and weakness with no abdominal pain or chest pain 20 days after delivery and had no history of hypertension during pregnancy and perinatal or prior heart disease. Postpartum cardiomyopathy and left ventricular dysfunction were diagnosed by imaging study and cardiac enzyme level. Finally, CT-scan was performed and showed aortic dissection. The patient underwent surgery and after surgery, she was alive without any problem. Conclusions: Patients with peripartum cardiomyopathy and aortic dissection could be cured with good medical care.
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