@article{oai:nagasaki-u.repo.nii.ac.jp:00016677,
 author = {Tomihara, Aki and Ashizawa, Naoto and Abe, Kuniko and Kinoshita, Naoe and Chihaya, Keisuke and Yonekura, Tsuyoshi and Fukae, Satoki and Ashizawa, Kazuto and Eishi, Kiyoyuki and Hayashi, Tomayoshi and Yano, Katsusuke},
 issue = {22},
 journal = {Internal Medicine},
 month = {Dec},
 note = {A 24-year-old pregnant woman with Marfans syndrome delivered by cesarean section during the 38th week of gestation. Although aortic root dilatation did not increase during pregnancy, three months after delivery, 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 dissection, even after more than four months of β-blockade., Internal Medicine, vol.45(22), pp.1285-1289; 2006},
 pages = {1285--1289},
 title = {Risk of Development of Abdominal Aortic Aneurysm and Dissection of Thoracic Aorta in a Postpartum Womanwith Marfans Syndrome},
 volume = {45},
 year = {2006}
}