Skip to main content
Erschienen in: Pediatric Radiology 9/2019

05.06.2019 | Original Article

Characterisation of computed tomography angiography findings in paediatric patients with heterotaxy

verfasst von: Carlos F. Ugas Charcape, Larry R. Alpaca Rodriguez, Irma A. Matos Rojas, Claudia I. Lazarte Rantes, Melissa Valdez Quintana, Doris A. Katekaru Tokeshi, Monica Epelman

Erschienen in: Pediatric Radiology | Ausgabe 9/2019

Einloggen, um Zugang zu erhalten

Abstract

Background

Heterotaxy refers to the abnormal arrangement of organs across the left–right axis and is typically associated with complex cardiovascular malformations.

Objective

To characterise the range of cardiac and extracardiac CT angiography findings in children with heterotaxy using the latest nomenclature consensus and to compare the different types of isomerism.

Materials and methods

We retrospectively analysed the data of 64 consecutive paediatric patients referred to our tertiary paediatric cardiovascular centre who underwent CT angiography for the evaluation of known or suspected heterotaxy within a 52-month period.

Results

Right atrial isomerism was identified in 44 (69%) children, while left atrial isomerism was identified in 18 (28%) children. Atrial appendage anatomy and situs could not be determined in 2 children (3%). Associated heart defects included complete atrioventricular canal (CAVC) in 51 (80%) children, total anomalous pulmonary venous return in 43 (67%) and pulmonary atresia in 23 (36%). The bronchial branching pattern corresponded to atrial appendage morphology in all children except in the two in whom atrial appendage morphology could not be defined. In children with right atrial isomerism, the most common associated abnormalities were CAVC (n=41, 93%) and asplenia (n=34, 77%), while in those with left atrial isomerism, the most common associated abnormalities were polysplenia (n=17, 94%) and an interrupted inferior vena cava with azygos continuation (n=15, 83%).

Conclusion

CT angiography provides useful cardiovascular and extracardiac data on heterotaxy, which frequently involves a pattern of side-related findings but has great anatomical variability.
Literatur
1.
Zurück zum Zitat Balan A, Lazoura O, Padley SP et al (2012) Atrial isomerism: a pictorial review. J Cardiovasc Comput Tomogr 6:127–136CrossRefPubMed Balan A, Lazoura O, Padley SP et al (2012) Atrial isomerism: a pictorial review. J Cardiovasc Comput Tomogr 6:127–136CrossRefPubMed
2.
Zurück zum Zitat Jacobs JP, Anderson RH, Weinberg PM et al (2007) The nomenclature, definition and classification of cardiac structures in the setting of heterotaxy. Cardiol Young 17:1–28PubMed Jacobs JP, Anderson RH, Weinberg PM et al (2007) The nomenclature, definition and classification of cardiac structures in the setting of heterotaxy. Cardiol Young 17:1–28PubMed
3.
Zurück zum Zitat Hong YK, Park YW, Ryu SJ et al (2000) Efficacy of MRI in complicated congenital heart disease with visceral heterotaxy syndrome. J Comput Assist Tomogr 24:671–682CrossRefPubMed Hong YK, Park YW, Ryu SJ et al (2000) Efficacy of MRI in complicated congenital heart disease with visceral heterotaxy syndrome. J Comput Assist Tomogr 24:671–682CrossRefPubMed
4.
5.
Zurück zum Zitat Ticho BS, Goldstein AM, Van Praagh R (2000) Extracardiac anomalies in the heterotaxy syndromes with focus on anomalies of midline-associated structures. Am J Cardiol 85:729–734CrossRefPubMed Ticho BS, Goldstein AM, Van Praagh R (2000) Extracardiac anomalies in the heterotaxy syndromes with focus on anomalies of midline-associated structures. Am J Cardiol 85:729–734CrossRefPubMed
6.
Zurück zum Zitat Sutherland MJ, Ware SM (2009) Disorders of left-right asymmetry: heterotaxy and situs inversus. Am J Med Genet C Semin Med Genet 151c:307–317CrossRefPubMed Sutherland MJ, Ware SM (2009) Disorders of left-right asymmetry: heterotaxy and situs inversus. Am J Med Genet C Semin Med Genet 151c:307–317CrossRefPubMed
7.
Zurück zum Zitat Burton EC, Olson M, Rooper L (2014) Defects in laterality with emphasis on heterotaxy syndromes with asplenia and polysplenia: an autopsy case series at a single institution. Pediatr Dev Pathol 17:250–264CrossRefPubMed Burton EC, Olson M, Rooper L (2014) Defects in laterality with emphasis on heterotaxy syndromes with asplenia and polysplenia: an autopsy case series at a single institution. Pediatr Dev Pathol 17:250–264CrossRefPubMed
8.
Zurück zum Zitat Han BK, Overman DM, Grant K et al (2013) Non-sedated, free breathing cardiac CT for evaluation of complex congenital heart disease in neonates. J Cardiovasc Comput Tomogr 7:354–360CrossRefPubMed Han BK, Overman DM, Grant K et al (2013) Non-sedated, free breathing cardiac CT for evaluation of complex congenital heart disease in neonates. J Cardiovasc Comput Tomogr 7:354–360CrossRefPubMed
9.
Zurück zum Zitat Zucker EJ, Koning JL, Lee EY (2017) Cyanotic congenital heart disease: essential primer for the practicing radiologist. Radiol Clin North Am 55:693–716CrossRefPubMed Zucker EJ, Koning JL, Lee EY (2017) Cyanotic congenital heart disease: essential primer for the practicing radiologist. Radiol Clin North Am 55:693–716CrossRefPubMed
10.
Zurück zum Zitat Malik A, Hellinger JC, Servaes S et al (2017) Prevalence of non-cardiovascular findings on CT angiography in children with congenital heart disease. Pediatr Radiol 47:267–279CrossRefPubMed Malik A, Hellinger JC, Servaes S et al (2017) Prevalence of non-cardiovascular findings on CT angiography in children with congenital heart disease. Pediatr Radiol 47:267–279CrossRefPubMed
11.
Zurück zum Zitat Bilotta F, Evered LA, Gruenbaum SE (2017) Neurotoxicity of anesthetic drugs: an update. Curr Opin Anaesthesiol 30:452–457CrossRefPubMed Bilotta F, Evered LA, Gruenbaum SE (2017) Neurotoxicity of anesthetic drugs: an update. Curr Opin Anaesthesiol 30:452–457CrossRefPubMed
12.
Zurück zum Zitat Houck CS, Vinson AE (2017) Anaesthetic considerations for surgery in newborns. Arch Dis Child Fetal Neonatal Ed 102:F359–f363CrossRefPubMed Houck CS, Vinson AE (2017) Anaesthetic considerations for surgery in newborns. Arch Dis Child Fetal Neonatal Ed 102:F359–f363CrossRefPubMed
13.
Zurück zum Zitat Olchowy C, Cebulski K, Lasecki M et al (2017) The presence of the gadolinium-based contrast agent depositions in the brain and symptoms of gadolinium neurotoxicity — a systematic review. PLoS One 12:e0171704CrossRefPubMedPubMedCentral Olchowy C, Cebulski K, Lasecki M et al (2017) The presence of the gadolinium-based contrast agent depositions in the brain and symptoms of gadolinium neurotoxicity — a systematic review. PLoS One 12:e0171704CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat Rossi Espagnet MC, Bernardi B, Pasquini L et al (2017) Signal intensity at unenhanced T1-weighted magnetic resonance in the globus pallidus and dentate nucleus after serial administrations of a macrocyclic gadolinium-based contrast agent in children. Pediatr Radiol 47:1345–1352CrossRefPubMed Rossi Espagnet MC, Bernardi B, Pasquini L et al (2017) Signal intensity at unenhanced T1-weighted magnetic resonance in the globus pallidus and dentate nucleus after serial administrations of a macrocyclic gadolinium-based contrast agent in children. Pediatr Radiol 47:1345–1352CrossRefPubMed
15.
Zurück zum Zitat Flood TF, Stence NV, Maloney JA, Mirsky DM (2017) Pediatric brain: repeated exposure to linear gadolinium-based contrast material is associated with increased signal intensity at unenhanced T1-weighted MR imaging. Radiology 282:222–228CrossRefPubMed Flood TF, Stence NV, Maloney JA, Mirsky DM (2017) Pediatric brain: repeated exposure to linear gadolinium-based contrast material is associated with increased signal intensity at unenhanced T1-weighted MR imaging. Radiology 282:222–228CrossRefPubMed
16.
Zurück zum Zitat Rose-Felker K, Robinson JD, Backer CL et al (2017) Preoperative use of CT angiography in infants with coarctation of the aorta. World J Pediatr Congenit Heart Surg 8:196–202CrossRefPubMed Rose-Felker K, Robinson JD, Backer CL et al (2017) Preoperative use of CT angiography in infants with coarctation of the aorta. World J Pediatr Congenit Heart Surg 8:196–202CrossRefPubMed
17.
Zurück zum Zitat Dyer KT, Hlavacek AM, Meinel FG et al (2014) Imaging in congenital pulmonary vein anomalies: the role of computed tomography. Pediatr Radiol 44:1158–1168CrossRefPubMed Dyer KT, Hlavacek AM, Meinel FG et al (2014) Imaging in congenital pulmonary vein anomalies: the role of computed tomography. Pediatr Radiol 44:1158–1168CrossRefPubMed
18.
Zurück zum Zitat Lee EY, Jenkins KJ, Muneeb M et al (2013) Proximal pulmonary vein stenosis detection in pediatric patients: value of multiplanar and 3-D VR imaging evaluation. Pediatr Radiol 43:929–936CrossRefPubMed Lee EY, Jenkins KJ, Muneeb M et al (2013) Proximal pulmonary vein stenosis detection in pediatric patients: value of multiplanar and 3-D VR imaging evaluation. Pediatr Radiol 43:929–936CrossRefPubMed
19.
Zurück zum Zitat Cohen MS, Anderson RH, Cohen MI et al (2007) Controversies, genetics, diagnostic assessment, and outcomes relating to the heterotaxy syndrome. Cardiol Young 17:29–43CrossRefPubMed Cohen MS, Anderson RH, Cohen MI et al (2007) Controversies, genetics, diagnostic assessment, and outcomes relating to the heterotaxy syndrome. Cardiol Young 17:29–43CrossRefPubMed
20.
Zurück zum Zitat Uemura H, Ho SY, Devine WA et al (1995) Atrial appendages and venoatrial connections in hearts from patients with visceral heterotaxy. Ann Thorac Surg 60:561–569CrossRefPubMed Uemura H, Ho SY, Devine WA et al (1995) Atrial appendages and venoatrial connections in hearts from patients with visceral heterotaxy. Ann Thorac Surg 60:561–569CrossRefPubMed
21.
Zurück zum Zitat Anderson RH (2000) Atrial structure in the presence of visceral heterotaxy. Cardiol Young 10:299–302CrossRefPubMed Anderson RH (2000) Atrial structure in the presence of visceral heterotaxy. Cardiol Young 10:299–302CrossRefPubMed
22.
Zurück zum Zitat Wolla CD, Hlavacek AM, Schoepf UJ et al (2013) Cardiovascular manifestations of heterotaxy and related situs abnormalities assessed with CT angiography. J Cardiovasc Comput Tomogr 7:408–416CrossRefPubMedPubMedCentral Wolla CD, Hlavacek AM, Schoepf UJ et al (2013) Cardiovascular manifestations of heterotaxy and related situs abnormalities assessed with CT angiography. J Cardiovasc Comput Tomogr 7:408–416CrossRefPubMedPubMedCentral
23.
Zurück zum Zitat Taylor GA (2011) CT appearance of the duodenum and mesenteric vessels in children with normal and abnormal bowel rotation. Pediatr Radiol 41:1378–1383CrossRefPubMed Taylor GA (2011) CT appearance of the duodenum and mesenteric vessels in children with normal and abnormal bowel rotation. Pediatr Radiol 41:1378–1383CrossRefPubMed
24.
Zurück zum Zitat Orzech N, Navarro OM, Langer JC (2006) Is ultrasonography a good screening test for intestinal malrotation? J Pediatr Surg 41:1005–1009CrossRefPubMed Orzech N, Navarro OM, Langer JC (2006) Is ultrasonography a good screening test for intestinal malrotation? J Pediatr Surg 41:1005–1009CrossRefPubMed
25.
Zurück zum Zitat Boone JM, Strauss KJ, Cody DD et al (2011) AAPM report 204: size-specific dose estimates (SSDE) in pediatric and adult body CT examinations. American Association of Physicists in Medicine, College Park Boone JM, Strauss KJ, Cody DD et al (2011) AAPM report 204: size-specific dose estimates (SSDE) in pediatric and adult body CT examinations. American Association of Physicists in Medicine, College Park
26.
Zurück zum Zitat Loomba RS, Hlavacek AM, Spicer DE, Anderson RH (2015) Isomerism or heterotaxy: which term leads to better understanding? Cardiol Young 25:1037–1043CrossRefPubMed Loomba RS, Hlavacek AM, Spicer DE, Anderson RH (2015) Isomerism or heterotaxy: which term leads to better understanding? Cardiol Young 25:1037–1043CrossRefPubMed
27.
Zurück zum Zitat Strouse PJ (2004) Disorders of intestinal rotation and fixation ("malrotation"). Pediatr Radiol 34:837–851CrossRefPubMed Strouse PJ (2004) Disorders of intestinal rotation and fixation ("malrotation"). Pediatr Radiol 34:837–851CrossRefPubMed
28.
Zurück zum Zitat Yim D, Nagata H, Lam CZ et al (2018) Disharmonious patterns of heterotaxy and isomerism: how often are the classic patterns breached? Circ Cardiovasc Imaging 11:e006917PubMed Yim D, Nagata H, Lam CZ et al (2018) Disharmonious patterns of heterotaxy and isomerism: how often are the classic patterns breached? Circ Cardiovasc Imaging 11:e006917PubMed
29.
Zurück zum Zitat Tremblay C, Loomba RS, Frommelt PC et al (2017) Segregating bodily isomerism or heterotaxy: potential echocardiographic correlations of morphological findings. Cardiol Young 27:1470–1480CrossRefPubMed Tremblay C, Loomba RS, Frommelt PC et al (2017) Segregating bodily isomerism or heterotaxy: potential echocardiographic correlations of morphological findings. Cardiol Young 27:1470–1480CrossRefPubMed
30.
Zurück zum Zitat Uemura H, Ho SY, Devine WA, Anderson RH (1995) Analysis of visceral heterotaxy according to splenic status, appendage morphology, or both. Am J Cardiol 76:846–849CrossRefPubMed Uemura H, Ho SY, Devine WA, Anderson RH (1995) Analysis of visceral heterotaxy according to splenic status, appendage morphology, or both. Am J Cardiol 76:846–849CrossRefPubMed
32.
Zurück zum Zitat Yildirim SV, Tokel K, Varan B et al (2007) Clinical investigations over 13 years to establish the nature of the cardiac defects in patients having abnormalities of lateralization. Cardiol Young 17:275–282CrossRefPubMed Yildirim SV, Tokel K, Varan B et al (2007) Clinical investigations over 13 years to establish the nature of the cardiac defects in patients having abnormalities of lateralization. Cardiol Young 17:275–282CrossRefPubMed
33.
Zurück zum Zitat Srivastava D, Preminger T, Lock JE et al (1995) Hepatic venous blood and the development of pulmonary arteriovenous malformations in congenital heart disease. Circulation 92:1217–1222CrossRefPubMed Srivastava D, Preminger T, Lock JE et al (1995) Hepatic venous blood and the development of pulmonary arteriovenous malformations in congenital heart disease. Circulation 92:1217–1222CrossRefPubMed
34.
Zurück zum Zitat Burstein DS, Mavroudis C, Puchalski MD et al (2011) Pulmonary arteriovenous malformations in heterotaxy syndrome: the case for early, direct hepatic vein-to-azygos vein connection. World J Pediatr Congenit Heart Surg 2:119–128CrossRefPubMed Burstein DS, Mavroudis C, Puchalski MD et al (2011) Pulmonary arteriovenous malformations in heterotaxy syndrome: the case for early, direct hepatic vein-to-azygos vein connection. World J Pediatr Congenit Heart Surg 2:119–128CrossRefPubMed
35.
Zurück zum Zitat McElhinney DB, Marx GR, Newburger JW (2011) Congenital portosystemic venous connections and other abdominal venous abnormalities in patients with polysplenia and functionally univentricular heart disease: a case series and literature review. Congenit Heart Dis 6:28–40CrossRefPubMed McElhinney DB, Marx GR, Newburger JW (2011) Congenital portosystemic venous connections and other abdominal venous abnormalities in patients with polysplenia and functionally univentricular heart disease: a case series and literature review. Congenit Heart Dis 6:28–40CrossRefPubMed
36.
Zurück zum Zitat McElhinney DB, Marx GR, Marshall AC et al (2011) Cavopulmonary pathway modification in patients with heterotaxy and newly diagnosed or persistent pulmonary arteriovenous malformations after a modified Fontan operation. J Thorac Cardiovasc Surg 141:1362–1370CrossRefPubMed McElhinney DB, Marx GR, Marshall AC et al (2011) Cavopulmonary pathway modification in patients with heterotaxy and newly diagnosed or persistent pulmonary arteriovenous malformations after a modified Fontan operation. J Thorac Cardiovasc Surg 141:1362–1370CrossRefPubMed
37.
Zurück zum Zitat Baban A, Cantarutti N, Adorisio R et al (2018) Long-term survival and phenotypic spectrum in heterotaxy syndrome: a 25-year follow-up experience. Int J Cardiol 268:100–105CrossRefPubMed Baban A, Cantarutti N, Adorisio R et al (2018) Long-term survival and phenotypic spectrum in heterotaxy syndrome: a 25-year follow-up experience. Int J Cardiol 268:100–105CrossRefPubMed
38.
Zurück zum Zitat Rameshbabu CS, Gupta KK, Qasim M, Gupta OP (2015) Heterotaxy polysplenia syndrome in an adult with unique vascular anomalies: case report with review of literature. J Radiol Case Rep 9:22–37PubMedPubMedCentral Rameshbabu CS, Gupta KK, Qasim M, Gupta OP (2015) Heterotaxy polysplenia syndrome in an adult with unique vascular anomalies: case report with review of literature. J Radiol Case Rep 9:22–37PubMedPubMedCentral
39.
Zurück zum Zitat Bartram U, Wirbelauer J, Speer CP (2005) Heterotaxy syndrome — asplenia and polysplenia as indicators of visceral malposition and complex congenital heart disease. Biol Neonate 88:278–290CrossRefPubMed Bartram U, Wirbelauer J, Speer CP (2005) Heterotaxy syndrome — asplenia and polysplenia as indicators of visceral malposition and complex congenital heart disease. Biol Neonate 88:278–290CrossRefPubMed
40.
Zurück zum Zitat Van Praagh S (1992) Cardiac malpositions and the heterotaxy syndromes. In: Keane J, Fyler D, Lock J (eds) Nadas’ pediatric cardiology, 2nd edn. Hanley & Belfus Inc. Mosby, Philadelphia, pp 589–608 Van Praagh S (1992) Cardiac malpositions and the heterotaxy syndromes. In: Keane J, Fyler D, Lock J (eds) Nadas’ pediatric cardiology, 2nd edn. Hanley & Belfus Inc. Mosby, Philadelphia, pp 589–608
Metadaten
Titel
Characterisation of computed tomography angiography findings in paediatric patients with heterotaxy
verfasst von
Carlos F. Ugas Charcape
Larry R. Alpaca Rodriguez
Irma A. Matos Rojas
Claudia I. Lazarte Rantes
Melissa Valdez Quintana
Doris A. Katekaru Tokeshi
Monica Epelman
Publikationsdatum
05.06.2019
Verlag
Springer Berlin Heidelberg
Erschienen in
Pediatric Radiology / Ausgabe 9/2019
Print ISSN: 0301-0449
Elektronische ISSN: 1432-1998
DOI
https://doi.org/10.1007/s00247-019-04434-0

Weitere Artikel der Ausgabe 9/2019

Pediatric Radiology 9/2019 Zur Ausgabe

Update Radiologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.