Key result
Emergency Bentall procedure during second-trimester pregnancy achieves maternal and fetal survival in Marfan syndrome.
Why the study?
Pregnancy in Marfan syndrome markedly increases the risk of aortic complications, creating management challenges when giant aortic aneurysms with severe aortic regurgitation are diagnosed before fetal viability.
Case Report (n=1)
No
Emergency aortic root replacement during early second-trimester pregnancy can be lifesaving for selected patients with Marfan syndrome and severe aortic pathology.
Supports emergency Bentall feasibility in select early second-trimester Marfan pregnancies; leaves open standardization and prospective outcome data.
Background Pregnancy in women with Marfan syndrome markedly increases the risk of life-threatening aortic complications due to superimposed haemodynamic and hormonal stress on an intrinsically fragile aortic wall. Management becomes particularly challenging when a giant aortic root or ascending aortic aneurysm with severe aortic regurgitation is diagnosed during early pregnancy before fetal viability. Case summary A 19-year-old primigravid woman at 15 weeks and 2 days of gestation with known Marfan syndrome presented with persistent palpitations. Evaluation revealed a giant fusiform aneurysm involving the aortic root and ascending aorta measuring 69 mm on transthoracic echocardiography and approximately 9–10 cm intraoperatively, severe aortic regurgitation due to annular dilation, and left ventricular systolic dysfunction with an ejection fraction of 40–42%. Following multidisciplinary consultation and counselling regarding maternal and fetal risks, urgent surgical intervention was undertaken without termination of pregnancy. The patient underwent an emergency Bentall procedure. The perioperative course was complicated by major bleeding requiring delayed sternal closure and transfusion support. Postoperative echocardiography demonstrated a functioning mechanical prosthesis with acceptable haemodynamics and persistent severe left ventricular systolic dysfunction with an ejection fraction of 25–30%. Obstetric ultrasonography confirmed a viable fetus. The patient was discharged in stable condition on postoperative day 11. Discussion This case demonstrates that emergency aortic root replacement during early second-trimester pregnancy may be lifesaving in selected patients with Marfan syndrome and severe aortic pathology when guided by multidisciplinary coordination and meticulous perioperative management.
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Mottahedi et al. (2026) conducted a case report in Marfan syndrome with giant aortic root aneurysm in pregnancy (n=1). Emergency Bentall procedure was evaluated on Maternal and fetal survival. Emergency Bentall procedure during early second-trimester pregnancy resulted in maternal survival and a viable fetus in a 19-year-old with Marfan syndrome and a giant aortic root aneurysm.
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