Cor Vasa 2012, 54(9-10):e329-e335 | DOI: 10.1016/j.crvasa.2012.07.002
Diagnostic problems in fetal visceral heterotaxy syndrome. Sonography vs. autopsy
- a Department of Descriptive and Clinical Anatomy, Center of Biostructure Research, Medical University of Warsaw, Poland
- b Perinatology and Prenatal Cardiology Unit, II Chair of Obstetrics and Gynecology, Medical University of Warsaw, Poland
Introduction: Visceral heterotaxy syndromes (VHS) are defined as abnormalities of the determination of left--
-right symmetry, described as left or right atrial isomerism (LAI, RAI) [11]. Some cases do not follow classical patterns and may cause diagnostic problems. The aim of this study is to determine whether their features can be helpful or misleading in the diagnosis of VHS.
Material and methods: The study was based on 6 cases diagnosed sonographically and/or in autopsy. The results of examinations were re-evaluated and compared.
Results: Two of 6 fetuses were diagnosed to have right atrial isomerism (RAI), 3 presented left atrial iso-merism (LAI) and one case was diagnosed as VHS. Cardiovascular anomalies comprised: abnormal systemic venous connections (6/6), partial anomalous pulmonary venous drainage (PAPVD) (2/6), complete atrioventricular septal defect (cAVSD) (2/6), ventricular left-hand pattern (2/6), ventriculo-arterial discordance (1/6), tricuspid atresia (1/6), mitral atresia (1/6) and tetralogy of Fallot (ToF) (1/6). Fetuses diagnosed as LAI presen-ted complete heart block. In 2 cases of RAI and in 3 cases of LAI isomeric anatomy of the atrial appendages was observed. None of fetuses with LAI presented "polysplenia" and none of fetuses with RAI presented "asplenia". Lungs and main bronchi were isomeric in 3 cases of LAI and in no cases of RAI. One fetus with otocephaly presented atrial situs solitus and multiple cardiac anomalies, situs ambiguus of lungs and bronchi and situs solitus of the abdominal viscera.
Conclusions: There are characteristic features of left and right isomerism, and they may be present in various forms. In some cases extracardiac features of VHS can be seen only on autopsy.
Keywords: Aplenia; Atrial isomerism; Congenital heart defect; Fetal echocardiography; Heterotaxy syndrome; Polysplenia
Received: April 20, 2012; Accepted: July 24, 2012; Published: September 1, 2012 Show citation
References
- B. Ferdman, L. States, J.W. Gaynor, et al., Abnormalities of intestinal rotation in patients with congenital heart disease and heterotaxy syndrome, Congenital Heart Disease 2 (2007) 12-18.
Go to original source...
Go to PubMed...
- B.I. Ivemark, Implications of agenesis of the spleen on the pathogenesis of cono-truncus anomalies in childhood, Acta Paediatrica Scandinavica 44 (Suppl. 104) (1955) 1-110.
Go to original source...
- L.H. Van Mierop, F.W.Wiglesworth, Isomerism of the cardiac atria in the asplenia syndrome, Laboratory Investigation 11 (1962) 1303-1315.
Go to PubMed...
- R. Van Praagh, S. Van Praagh, Atrial isomerism in the heterotaxy syndromes with asplenia, or polysplenia, or normally formed spleen: an erroneous concept, American Journal of Cardiology 66 (1990) 1504-1506.
Go to original source...
Go to PubMed...
- S. Van Praagh, F. Santini, S.P. Sanders, Cardiac malposition with special emphasis on visceral heterotaxy (asplenia and polysplenia syndromes), in: D.C. Fyler (Ed.), Nadas' Pediatric Cardiology. Hanley and Belfus, Philadelphia, 1992, pp. 589-608.
- S. Van Praagh, J. Kreutzer, L. Alday, R. Van Praagh, Systemic and pulmonary venous connections in visceral heterotaxy with emphasis on the diagnosis of the atrial situs: a study of 109 postmortem cases, in: E.B. Clark, A. Takao (Eds.), Developmental Cardiology Morphogenesis and Function, Futura, New York, 1990, pp. 671-727.
- E.A. Shinebourne, F.J. Macartney, R.H. Anderson, Sequential chamber localization - logical approach to diagnosis in congenital heart disease, British Heart Journal 38 (1976) 327-340.
Go to original source...
- S.M. De Tomassi, L. Daliento, S.Y. Ho, et al., Analysis of atrioventricular junction, ventricular mass, and ventriculoarterial junction in 43 specimens with atrial isomerism, British Heart Journal 45 (1981) 237-247.
Go to original source...
- H. Uemura, S.Y. Ho, W.A. Devine, R.H. Anderson, Analysis of visceral heterotaxy according to splenic status, appendage morphology, or both, American Journal of Cardiology 76 (1995) 846-849.
Go to original source...
Go to PubMed...
- H. Uemura, S.Y. Ho, W.A. Devine, et al., Atrial appendages and venoatrial connections in hearts from patients with visceral heterotaxy, Annals of Thoracic Surgery 60 (1995) 561-569.
Go to original source...
Go to PubMed...
- H. Uemura, S.Y. Ho, R.H. Anderson, T. Yagihara, Ventricular morphology and coronary arterial anatomy in hearts with isomeric atrial appendages, Annals of Thoracic Surgery 67 (1999) 1403-1411.
Go to original source...
Go to PubMed...
- J.P. Jacobs, R.H. Anderson, P.M. Weinberg, et al., The nomenclature, definition and classification of cardiac structures in the setting of heterotaxy, Cardiology in the Young 17 (suppl 2) (2007) 1-28.
Go to original source...
Go to PubMed...
- J.H. Lin, C.I. Chang, J.K. Wang, et al., Intrauterine diagnosis of heterotaxy syndrome, American Heart Journal 143 (2002) 1002-1008.
Go to original source...
Go to PubMed...
- M.S. Cohen, Clarifying anatomical complexity: diagnosing heterotaxy syndrome in the fetus, Progress in Pediatric Cardiology 22 (2006) 61-70.
Go to original source...
- R.H. Anderson, How should we optimally describe complex congenitally malformed hearts?, Annals of Thoracic Surgery 62 (1996) 710-716.
Go to original source...
Go to PubMed...
- C. Schiffer, G. Tariverdian, M. Schiesser, et al., Agnathia-otocephaly complex: report of three cases with involvement of two different Carnegie stages, American Journal of Medical Genetics 112 (2002) 203-208.
Go to original source...
Go to PubMed...
- L. Zhu, M.J. Marvin, A. Gardiner, et al., Cerberus regulates left-right asymmetry of the embryonic head and heart, Current Biology 9 (1999) 931-938.
Go to original source...
Go to PubMed...
- R.V. Pearse, K.J. Vogan, C.J. Tabin, Ptc1 and Ptc2 transcripts provide distinct readouts of hedgehog signaling activity during chick embryogenesis, Developmental Biology 239 (2001) 15-29.
Go to original source...
Go to PubMed...
- R.H. Anderson, H. Uemura, S.Y. Ho, et al., Asplenia syndrome, American Journal of Cardiology 74 (10) (1994) 1079.
Go to original source...
- U. Bartram, J. Wirbelauer, C.P. Speer, et al., Heterotaxy syndrome - asplenia and polysplenia as indicators of visceral malposition and complex congenital heart disease, Biology of the Neonate 88 (2005) 278-290.
Go to original source...
Go to PubMed...
- L.H.S. Van Mierop, I.H. Gessner, G.L. Schiebler, Asplenia and polysplenia syndromes, in: Bergsma (Ed.), Birth Defects, Original Articles Series, Williams and Wilkins, Baltimore, 1972, pp. 72-84.
- H. Uemura, S.Y. Ho, W.A. Devine, et al., Atrial appendages and venoatrial connections in hearts from patients with visceral heterotaxy, Annals of Thoracic Surgery 60 (1995) 561-569.
Go to original source...
Go to PubMed...
- S. Meryl, M. Cohen, Clarifying anatomical complexity: diagnosing heterotaxy syndrome in the fetus, Progress in Pediatric Cardiology 22 (2006) 61-70.
Go to original source...
- S. Swaminathan, A. Parthiban, et al., Progressive fetal atrioventricular block in heterotaxy syndrome, Cardiology in the Young 17 (2007) 432-434.
Go to original source...
Go to PubMed...
- M. Taketazu, J. Lougheed, S.J. Yoo, et al., Spectrum of cardiovascular disease, accuracy of diagnosis and outcome in fetal heterotaxy syndrome, American Journal of Cardiology 97 (2006) 720-724.
Go to original source...
Go to PubMed...
- E. Goldmuntz, R. Bamford, J.D. Karkera, et al., CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle, American Journal of Human Genetics 70 (2002) 776-780.
Go to original source...
Go to PubMed...
- A.E. Urban, R.H. Anderson, J. Stark, et al., Double-outlet left ventricle associated with situs inversus and atrioventricular concordance, American Heart Journal 95 (1) (1977) 91-95.
Go to original source...
- J.W. Belmont, B. Mohapatra, J.A. Towbin, S.M. Ware, et al., Molecular genetics of heterotaxy syndromes, Current Opinion in Cardiology 19 (2004) 216-220.
Go to original source...
Go to PubMed...
- B.D. Gelb, et al., Genetic basis of congenital heart disease, Current Opinion in Cardiology 19 (2004) 110-115.
Go to original source...
Go to PubMed...
- E. Goldmuntz, B.J. Clark, L.E. Mitchell, et al., Frequency of 22q11 deletions in patients with conotruncal defects, Journal of the American College of Cardiology 32 (1998) 492-498.
Go to original source...
Go to PubMed...
- M.E. Pierpont, C.T. Basson, D.W. Benson Jr, et al., Genetic basis for congenital heart defects: current knowledge, Circulation 115 (2007) 3015-3038.
Go to original source...
Go to PubMed...
- M.E. Pierpont, et al., Genetic etiology of cardiac syndromes, Progress in Pediatric Cardiology 6 (1996) 29-41.
Go to original source...