CC BY-NC-ND 4.0 · AJP Rep 2019; 09(02): e121-e126
DOI: 10.1055/s-0038-1677480
Case Report
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Prenatal Diagnosis and Successful Palliation of Absent Aortic Valve with Hypoplastic Left Heart Syndrome: A Case Report and Review of Literature

1   Department of Pediatrics, University of Texas Medical Branch, Galveston, Texas
,
Chelsea B. Johnson
1   Department of Pediatrics, University of Texas Medical Branch, Galveston, Texas
,
Muhammad A. Aly
1   Department of Pediatrics, University of Texas Medical Branch, Galveston, Texas
,
2   Division of Pediatric Cardiology, University of Texas Medical Branch, Galveston, Texas
› Institutsangaben
Weitere Informationen

Publikationsverlauf

12. September 2018

02. Dezember 2018

Publikationsdatum:
09. April 2019 (online)

Abstract

Introduction Congenital absence of the aortic valve leaflets is a rare association with hypoplastic left heart syndrome (HLHS).

Case A 37-year-old pregnant woman was referred for fetal evaluation of possible HLHS at 22 weeks of gestation. The fetal echocardiogram (ECHO) was remarkable for a hypoplastic left atrium, nearly atretic mitral valve, small left ventricle, and a hypoplastic aortic valve with severe aortic insufficiency. A female infant was born at term and postnatal ECHO confirmed the above findings. In addition, there was complete absence of the aortic valve leaflets. The patient underwent Norwood's procedure at day 5 of life with atrial septectomy, over-sewing of the aortic valve annulus, and a 4 mm Sano's shunt between the right ventricle and the main pulmonary artery. She tolerated this surgery well and subsequently underwent a bidirectional Glenn's procedure at 8 months of life.

Conclusion Prenatal diagnosis of absent aortic valve should be suspected in the presence of severe aortic insufficiency in the fetal ECHO. Early postnatal intervention is critical as those patients are likely to deteriorate quickly. The over-sewing of the aortic valve may be important to prevent coronary steal and myocardial hypoperfusion which could potentially be detrimental.

Ethical Approval

This article does not contain any studies with human participants performed by any of the authors.


Informed Consent

Informed consent was waived for this study since no identifying information was included.


 
  • References

  • 1 Murakami T, Horigome H, Shiono J. , et al. Prenatal diagnosis of congenital absence of aortic valve: a report of two cases with different outcomes and a literature review. Fetal Diagn Ther 2015; 38 (04) 307-314
  • 2 Harada Y, Takeuchi T, Satomi G, Yasukouchi S. Absent aortic valve: successful palliation in the neonate. Ann Thorac Surg 1998; 66 (03) 935-936
  • 3 Krasemann T, Kehl HG, Hammel D, Asfour B. Congenital aortic regurgitation due to absent aortic cusps and high-degree mitral stenosis. Pediatr Cardiol 2003; 24 (03) 304-306
  • 4 Maulik D, Nanda NC, Maulik D, Vilchez G. A brief history of fetal echocardiography and its impact on the management of congenital heart disease. Echocardiography 2017; 34 (12) 1760-1767
  • 5 Liu H, Zhou J, Feng QL. , et al. Fetal echocardiography for congenital heart disease diagnosis: a meta-analysis, power analysis and missing data analysis. Eur J Prev Cardiol 2015; 22 (12) 1531-1547
  • 6 Holland BJ, Myers JA, Woods Jr CR. Prenatal diagnosis of critical congenital heart disease reduces risk of death from cardiovascular compromise prior to planned neonatal cardiac surgery: a meta-analysis. Ultrasound Obstet Gynecol 2015; 45 (06) 631-638
  • 7 Toews WH, Lortscher RH, Kelminson LL. Double outlet right ventricle with absent aortic valve. Chest 1975; 68 (03) 381-382
  • 8 Bierman FZ, Yeh MN, Swersky S, Martin E, Wigger JH, Fox H. Absence of the aortic valve: antenatal and postnatal two-dimensional and Doppler echocardiographic features. J Am Coll Cardiol 1984; 3 (03) 833-837
  • 9 Rossi MB, Ho SY, Tasker RC. Absent aortic valve leaflets. Int J Cardiol 1986; 11 (02) 235-237
  • 10 Niwa K, Ikeda F, Miyamoto H, Nakajima H, Ando M. Absent aortic valve with normally related great arteries. Heart Vessels 1987; 3 (02) 104-107
  • 11 Weintraub RG, Chow CW, Gow RM. Absence of the leaflets of the aortic valve in DiGeorge syndrome. Int J Cardiol 1989; 23 (02) 255-257
  • 12 Cabrera A, Galdeano JM, Pastor E. Absence of the aortic valve cusps with mitral atresia, normal left ventricle, and intact ventricular septum. Br Heart J 1990; 63 (03) 187-188
  • 13 Parikh SR, Hurwitz RA, Caldwell RL, Waller B. Absent aortic valve in hypoplastic left heart syndrome. Am Heart J 1990; 119 (04) 977-978
  • 14 Lin AE, Chin AJ. Absent aortic valve: a complex anomaly. Pediatr Cardiol 1990; 11 (04) 195-198
  • 15 Hartwig NG, Vermeij-Keers C, De Vries HE, Gittenberger-De Groot AC. Aplasia of semilunar valve leaflets: two case reports and developmental aspects. Pediatr Cardiol 1991; 12 (02) 114-117
  • 16 Miyabara S, Ando M, Yoshida K, Saito N, Sugihara H. Absent aortic and pulmonary valves: investigation of three fetal cases with cystic hygroma and review of the literature. Heart Vessels 1994; 9 (01) 49-55
  • 17 Marek J, Skovránek J, Povýsilová V. Congenital absence of aortic and pulmonary valve in a fetus with severe heart failure. Heart 1996; 75 (01) 98-100
  • 18 Nakagawa M, Okamoto N, Fujino H. , et al. Doppler echocardiographic evaluation of the hemodynamics in absent aortic valve. Can J Cardiol 1999; 15 (11) 1283-1286
  • 19 Rouillard KP, Moore P, Silverman NH. Congenital absence of aortic valvar leaflets: a rare variant of the hypoplastic left heart syndrome. Cardiol Young 2001; 11 (04) 453-457
  • 20 Eronen M, Heikkilä P. Absent aortic and dysplastic pulmonary valves associated with ventricular septal defect in fetal hydrops. Pediatr Cardiol 2003; 24 (04) 400-402
  • 21 Hibino N, Harada Y, Hiramatsu T, Yasukochi S, Satomi G. Fontan operation for hypoplastic left heart syndrome with absent aortic valve. J Thorac Cardiovasc Surg 2004; 128 (02) 315-316
  • 22 Muneuchi J, Kuraoka A, Ochiai Y, Nishibatake M, Sese A, Joo K. Fatal systemic air embolism in a neonate with absent aortic valve. Pediatr Cardiol 2011; 32 (06) 839-841
  • 23 Sabati AA, Wong PC, Randolph L, Pruetz JD. Absent aortic valve associated with double outlet right ventricle and aortopulmonary window: physiologic implications of a rare malformation in both the fetus and neonate. Congenit Heart Dis 2014; 9 (03) E98-E104