Kötter-Thomsen I, Weisner D, Lehmann-Willenbrock E, Swalve S, von Hehn A
Abteilung Frauenheilkunde, Kiel.
Geburtshilfe Frauenheilkd. 1991 Aug;51(8):653-4. doi: 10.1055/s-2007-1026417.
Pregnant women with a Marfan syndrome carry a risk of developing an aortic arc dissection. As the developing aneurism may be diagnosed by echocardiography, this method should be applied repeatedly during pregnancy. We report the case of a Marfan patient, who developed an acute aortic dissection during the third trimester of her pregnancy and discuss the guidance and surveillance of Marfan patients who are or wish to become pregnant.
患有马凡综合征的孕妇有发生主动脉弓夹层的风险。由于发育中的动脉瘤可通过超声心动图诊断，因此在孕期应反复应用该方法。我们报告一例马凡综合征患者，她在妊娠晚期发生了急性主动脉夹层，并讨论了对已怀孕或希望怀孕的马凡综合征患者的指导和监测。
