Background <p>Pulmonary stenosis (PS) is a common congenital heart defect, often detectable prenatally via fetal echocardiography. This case report describes a fetus diagnosed at 19 weeks with severe valvular PS. Postnatal balloon valvuloplasty was successfully performed via jugular access due to femoral obstruction.</p> Case presentation <p>A 34-year-old pregnant woman was referred at 19 weeks due to increased fetal nuchal translucency, and fetal echocardiography revealed severe pulmonary stenosis with right ventricular hypertrophy and tricuspid regurgitation. After full-term vaginal delivery, the neonate’s diagnosis was confirmed, and progressive stenosis necessitated balloon valvuloplasty via jugular access due to lower venous obstruction. Post-procedure infundibular stenosis was managed medically with propranolol, resulting in significant gradient reduction, and the infant remains well on follow-up.</p> Conclusion <p>This case highlights the importance of fetal echocardiography, alternative venous access, and multidisciplinary care in achieving good outcomes in complex congenital heart disease.</p>

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Prenatal diagnosis and postnatal management of a complicated pulmonary valve stenosis: a case report

  • Alireza Golbabaei,
  • Hooman Mohammad Talebi

摘要

Background

Pulmonary stenosis (PS) is a common congenital heart defect, often detectable prenatally via fetal echocardiography. This case report describes a fetus diagnosed at 19 weeks with severe valvular PS. Postnatal balloon valvuloplasty was successfully performed via jugular access due to femoral obstruction.

Case presentation

A 34-year-old pregnant woman was referred at 19 weeks due to increased fetal nuchal translucency, and fetal echocardiography revealed severe pulmonary stenosis with right ventricular hypertrophy and tricuspid regurgitation. After full-term vaginal delivery, the neonate’s diagnosis was confirmed, and progressive stenosis necessitated balloon valvuloplasty via jugular access due to lower venous obstruction. Post-procedure infundibular stenosis was managed medically with propranolol, resulting in significant gradient reduction, and the infant remains well on follow-up.

Conclusion

This case highlights the importance of fetal echocardiography, alternative venous access, and multidisciplinary care in achieving good outcomes in complex congenital heart disease.