Acute Aortic Dissection (Type II) in a Pregnant Woman with the Marfan's Syndrome: Case Study and Literature Review

1993 ◽  
Vol 27 (7) ◽  
pp. 555-559 ◽  
Author(s):  
Iris C. Maurer ◽  
Alexander Bernhard
2018 ◽  
Vol 08 (04) ◽  
pp. e234-e240 ◽  
Author(s):  
Dominique Williams ◽  
Kathryn Lindley ◽  
Melissa Russo ◽  
Jennifer Habashi ◽  
Harry Dietz ◽  
...  

Objectives We sought to characterize pregnancy-related aortic complications in women with Marfan's syndrome who had prior aortic root replacement. Study Design This is a retrospective case series study and literature review of women with Marfan's syndrome with pregnancy after aortic root replacement. We surveyed women with Marfan's syndrome who had successful pregnancy after aortic root replacement using the Marfan Foundation Website and from two large tertiary care Marfan's clinics. Clinical data, counseling information, and details of pregnancy-related aortic complications were compiled. A literature review was performed assessing aortic outcomes in women with Marfan's syndrome with pregnancy after aortic surgery. Results Fourteen women with 20 pregnancies were identified. Two women had three pregnancies following root replacement for aortic dissection. There were no aortic dissections during the 20 pregnancies. In contrast, aortic dissection was frequently reported in the literature. Conclusions Women with Marfan's syndrome who become pregnant following aortic root replacement remain at risk for distal aortic dissection related to pregnancy. The exact risk is difficult to quantify but is not zero and women should be counseled accordingly.


2005 ◽  
Vol 53 (4) ◽  
pp. 220-222 ◽  
Author(s):  
Masayuki Sakaguchi ◽  
Hiroto Kitahara ◽  
Takayuki Watanabe ◽  
Tetsuya Kono ◽  
Daisuke Fukui ◽  
...  

Author(s):  
Riki Sumiyoshi ◽  
Hideki Morita ◽  
Kento Fujii ◽  
Takehiro Shirasughi ◽  
Hiroyuki Kawaura ◽  
...  

AbstractThe patient was a 31-year-old pregnant woman who gave birth to her first child by vaginal delivery 7 years ago. She was diagnosed with Marfan’s syndrome based on physical findings; however, the condition was not diagnosed before the onset. The patient developed acute aortic dissection at 28 weeks of pregnancy. A cesarean section was first performed to save the patient’s life; then, a total hysterectomy was performed to prevent the risk of postpartum hemorrhage. Furthermore, aortic root replacement was performed using a temporary mechanical valve. The patient and her child have survived without any complications.


2002 ◽  
Vol 31 (4) ◽  
pp. 282-284
Author(s):  
Shun-ichiro Sakamoto ◽  
Masami Ochi ◽  
Naoko Okubo ◽  
Yosuke Ishii ◽  
Ryuzo Bessho ◽  
...  

2005 ◽  
Vol 34 (2) ◽  
pp. 116-119
Author(s):  
Takahiro Inoue ◽  
Yoshimasa Sakamoto ◽  
Hiroshi Okuyama ◽  
Makoto Hanai ◽  
Noriyasu Kawada ◽  
...  

2008 ◽  
Vol 37 (2) ◽  
pp. 132-135 ◽  
Author(s):  
Masahiro Ryugo ◽  
Hiroshi Imagawa ◽  
Takahiro Shiozaki ◽  
Fumiaki Shikata ◽  
Kanji Kawachi

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