A 24-year-old pregnant woman with Marfan’s syndrome delivered by cesarean section during the 38th week of gestation. Although aortic root dilatation did not increase during pregnancy, three months after deliv-ery, the patient noticed a pulsatile abdominal mass. Aortic aneurysm was diagnosed and surgical replacement of the infrarenal abdominal aorta to the common iliac arteries and reconstruction of the inferior mesenteric artery were performed. Moreover, the patient subsequently developed a Stanford type B thoracic aortic dis-section, even after more than four months of β-blockade. Key words: Marfan’s syndrome, postpartum, abdominal aortic aneurysm, descending thoracic aortic dissec-tio
ArticleEuropean journal of cardio-thoracic surgery. 28(2): 280-283 (2005)journal articl
Acute aortic dissection in pregnancy is a rare event and rarer still in healthy young women; however...
Introduction: Aortic dissection is a rare cardiovascular complication in pregnancy. Most of the case...
A 24-year-old pregnant woman with Marfans syndrome delivered by cesarean section during the 38th wee...
In the current article, 3 cases of aortic aneurysm and dissection in pregnant patients with Marfan’s...
Aortic dissection can occur in pregnancy or during the postpartum period without pre-existing diseas...
Marfan syndrome is a heritable connective tissue disorder.The cardiovascular effects are life-threat...
SummaryA 36-year-old female patient known to have Marfan syndrome (MFS) presented with Stanford type...
Aortic dissection during pregnancy is rare but can be life-threatening to both the mother and the fo...
Objective: To describe perioperative management for type A aortic dissection in a postpartum woman w...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Stanford type A acute aortic dissection (AAD) is a very rare complication, with potentially lethal c...
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/139073/1/jah31693.pdfhttps://deepblue....
Pregnant patients with Marfan syndrome (MFS) are at high risk of developing aortic dissection or rup...
Marfan syndrome is a congenital disorder of the connective tissue involving the ocular, skeletal and...
ArticleEuropean journal of cardio-thoracic surgery. 28(2): 280-283 (2005)journal articl
Acute aortic dissection in pregnancy is a rare event and rarer still in healthy young women; however...
Introduction: Aortic dissection is a rare cardiovascular complication in pregnancy. Most of the case...
A 24-year-old pregnant woman with Marfans syndrome delivered by cesarean section during the 38th wee...
In the current article, 3 cases of aortic aneurysm and dissection in pregnant patients with Marfan’s...
Aortic dissection can occur in pregnancy or during the postpartum period without pre-existing diseas...
Marfan syndrome is a heritable connective tissue disorder.The cardiovascular effects are life-threat...
SummaryA 36-year-old female patient known to have Marfan syndrome (MFS) presented with Stanford type...
Aortic dissection during pregnancy is rare but can be life-threatening to both the mother and the fo...
Objective: To describe perioperative management for type A aortic dissection in a postpartum woman w...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Stanford type A acute aortic dissection (AAD) is a very rare complication, with potentially lethal c...
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/139073/1/jah31693.pdfhttps://deepblue....
Pregnant patients with Marfan syndrome (MFS) are at high risk of developing aortic dissection or rup...
Marfan syndrome is a congenital disorder of the connective tissue involving the ocular, skeletal and...
ArticleEuropean journal of cardio-thoracic surgery. 28(2): 280-283 (2005)journal articl
Acute aortic dissection in pregnancy is a rare event and rarer still in healthy young women; however...
Introduction: Aortic dissection is a rare cardiovascular complication in pregnancy. Most of the case...