Skip to main content
Top
Published in: Pediatric Radiology 8/2016

01-07-2016 | Original Article

CT-defined phenotype of pulmonary artery stenoses in Alagille syndrome

Authors: Renee M. Rodriguez, Jeffrey A. Feinstein, Frandics P. Chan

Published in: Pediatric Radiology | Issue 8/2016

Login to get access

Abstract

Background

Alagille syndrome is a rare disorder commonly associated with pulmonary artery stenosis. Studies exist discussing the cardiovascular sequela but no consistent phenotype, or pattern of pulmonary artery stenosis, has been described.

Objective

The objective of this study was to characterize the distribution and severity of pulmonary artery stenosis in patients with Alagille syndrome based on computed tomography angiography.

Materials and methods

A retrospective chart review identified patients with Alagille syndrome who had undergone CT angiography. Pulmonary trunk (MPA), left main pulmonary artery (LPA) and right main pulmonary artery (RPA) diameters in Alagille patients were compared with those from matched control subjects. Stenoses at lobar and segmental pulmonary arteries were categorized as: Grade 1 (<33% stenosis), Grade 2 (33-66% stenosis) or Grade 3 (>66% stenosis). Involvement among the different lung regions was then compared.

Results

Fifteen patients ages 6 months to 17 years were identified; one had surgical augmentation of the central pulmonary arteries and was excluded from the central (main, right and left) pulmonary artery analysis. The proximal LPA and RPA, but not the MPA, were significantly smaller than those of the control subjects (P<0.01). The proximal LPA was significantly smaller than the proximal RPA (P<0.01) in the Alagille group (0.55 LPA:RPA ratio). Within the Alagille group, 75% of the lobar and segmental branches showed mild or no stenoses (Grade 1), 17% showed moderate stenosis (Grade 2) and 8% showed severe stenosis (Grade 3). While not statistically significant, the right lung demonstrated a greater percentage of Grades 2 and 3 stenoses (28%, right vs. 20% left, P=0.1). The right middle and lingula lobes of both lungs showed more Grade 2 and 3 stenoses (33% upper/middle vs. 18% lower, P<0.01).

Conclusion

We describe a common pattern pulmonary artery stenosis in Alagille patients consisting of severe proximal LPA stenosis, heavy involvement of the lobar and segmental branches (more often right than left), and a greater involvement of the upper lobes. Knowledge of this phenotypic pattern can help in the diagnosis of Alagille syndrome in patients presenting with pulmonary artery stenosis.
Literature
1.
go back to reference Online Mendelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM Number: 118450: 1/30/2014. World Wide Web URL: http://omim.org/ Online Mendelian Inheritance in Man, OMIM®. Johns Hopkins University, Baltimore, MD. MIM Number: 118450: 1/30/2014. World Wide Web URL: http://​omim.​org/​
2.
go back to reference Crosnier C, Attié-Bitach T, Encha-Razavi F et al (2004) JAGGED1 gene expression during human embryogenesis elucidates the wide phenotypic spectrum of Alagille syndrome. Hepatology 32:574–581CrossRef Crosnier C, Attié-Bitach T, Encha-Razavi F et al (2004) JAGGED1 gene expression during human embryogenesis elucidates the wide phenotypic spectrum of Alagille syndrome. Hepatology 32:574–581CrossRef
3.
go back to reference McElhinney DB, Krantz ID, Bason L et al (2002) Analysis of cardiovascular phenotype and genotype–phenotype correlation in individuals with a JAG1 mutation and/or Alagille syndrome. Circulation 106:2567–2574CrossRefPubMed McElhinney DB, Krantz ID, Bason L et al (2002) Analysis of cardiovascular phenotype and genotype–phenotype correlation in individuals with a JAG1 mutation and/or Alagille syndrome. Circulation 106:2567–2574CrossRefPubMed
4.
go back to reference Alagille D, Estrada A, Hadchouel M et al (1987) Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases. J Pediatr 110:195–200CrossRefPubMed Alagille D, Estrada A, Hadchouel M et al (1987) Syndromic paucity of interlobular bile ducts (Alagille syndrome or arteriohepatic dysplasia): review of 80 cases. J Pediatr 110:195–200CrossRefPubMed
6.
go back to reference Oda T, Elkahloun AG, Pike BL et al (1997) Mutations in the human Jagged1 gene are responsible for Alagille syndrome. Nat Genet 16:235–242CrossRefPubMed Oda T, Elkahloun AG, Pike BL et al (1997) Mutations in the human Jagged1 gene are responsible for Alagille syndrome. Nat Genet 16:235–242CrossRefPubMed
7.
go back to reference Emerick KM, Rand EB, Goldmuntz E et al (1999) Features of Alagille syndrome in 92 patients: frequency and relation to prognosis. Hepatology 29:822–829CrossRefPubMed Emerick KM, Rand EB, Goldmuntz E et al (1999) Features of Alagille syndrome in 92 patients: frequency and relation to prognosis. Hepatology 29:822–829CrossRefPubMed
9.
10.
go back to reference Kamath BM, Spinner NB, Emerick KM et al (2004) Vascular anomalies in Alagille syndrome a significant cause of morbidity and mortality. Circulation 109:1354–1358CrossRefPubMed Kamath BM, Spinner NB, Emerick KM et al (2004) Vascular anomalies in Alagille syndrome a significant cause of morbidity and mortality. Circulation 109:1354–1358CrossRefPubMed
11.
go back to reference Deak PD, Smal Y, Kalender WA (2010) Multisection CT protocols: sex- and age-specific conversion factors used to determine effective dose from dose-length product. Radiology 257:158–166CrossRefPubMed Deak PD, Smal Y, Kalender WA (2010) Multisection CT protocols: sex- and age-specific conversion factors used to determine effective dose from dose-length product. Radiology 257:158–166CrossRefPubMed
12.
go back to reference Boone J, Strauss K, Cody D et al (2011) Size-specific dose estimates (SSDE) in pediatric and adult body CT exams. Report of AAPM Task Group 204 Boone J, Strauss K, Cody D et al (2011) Size-specific dose estimates (SSDE) in pediatric and adult body CT exams. Report of AAPM Task Group 204
13.
go back to reference Sluysmans T, Colan SD (2009) Structural measurements and adjustment for growth. In: Lai WW, Cohen MS, Geva T, Mertens L (eds) Echocardiography in pediatric and congenital heart disease. Wiley-Blackwell, West Sussex, UK, pp 53–63 Sluysmans T, Colan SD (2009) Structural measurements and adjustment for growth. In: Lai WW, Cohen MS, Geva T, Mertens L (eds) Echocardiography in pediatric and congenital heart disease. Wiley-Blackwell, West Sussex, UK, pp 53–63
14.
go back to reference Morrow D, Guha S, Sweeney C et al (2008) Notch and vascular smooth muscle cell phenotype. Circ Res 103:1370–1382CrossRefPubMed Morrow D, Guha S, Sweeney C et al (2008) Notch and vascular smooth muscle cell phenotype. Circ Res 103:1370–1382CrossRefPubMed
15.
go back to reference Tricarico F, Hlavacek AM, Schoepf UJ et al (2013) Cardiovascular CT angiography in neonates and children: image quality and potential for radiation dose reduction with iterative image reconstruction techniques. Eur Radiol 23:1306–1315CrossRefPubMed Tricarico F, Hlavacek AM, Schoepf UJ et al (2013) Cardiovascular CT angiography in neonates and children: image quality and potential for radiation dose reduction with iterative image reconstruction techniques. Eur Radiol 23:1306–1315CrossRefPubMed
16.
go back to reference Mayo J, Thakur Y (2013) Pulmonary CT angiography as first-line imaging for PE: image quality and radiation dose considerations. AJR Am J Roentgenol 200:522–528CrossRefPubMed Mayo J, Thakur Y (2013) Pulmonary CT angiography as first-line imaging for PE: image quality and radiation dose considerations. AJR Am J Roentgenol 200:522–528CrossRefPubMed
17.
go back to reference Nawaz A, Litt HI, Stavropoulos SW et al (2008) Digital subtraction pulmonary arteriography versus multidetector CT in the detection of pulmonary arteriovenous malformations. J Vasc Interv Radiol 19:1582–1588CrossRefPubMed Nawaz A, Litt HI, Stavropoulos SW et al (2008) Digital subtraction pulmonary arteriography versus multidetector CT in the detection of pulmonary arteriovenous malformations. J Vasc Interv Radiol 19:1582–1588CrossRefPubMed
18.
go back to reference Chandrashekhar G, Sodhi KS, Saxena AK et al (2012) Correlation of 64 row MDCT, echocardiography and cardiac catheterization angiography in assessment of pulmonary arterial anatomy in children with cyanotic congenital heart disease. Eur J Radiol 81:4211–4217CrossRefPubMed Chandrashekhar G, Sodhi KS, Saxena AK et al (2012) Correlation of 64 row MDCT, echocardiography and cardiac catheterization angiography in assessment of pulmonary arterial anatomy in children with cyanotic congenital heart disease. Eur J Radiol 81:4211–4217CrossRefPubMed
19.
go back to reference 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
20.
go back to reference Monge MC, Mainwaring RD, Sheikh AY et al (2013) Surgical reconstruction of peripheral pulmonary artery stenosis in Williams and Alagille syndromes. J Thorac Cardiovasc Surg 145:476–481CrossRefPubMed Monge MC, Mainwaring RD, Sheikh AY et al (2013) Surgical reconstruction of peripheral pulmonary artery stenosis in Williams and Alagille syndromes. J Thorac Cardiovasc Surg 145:476–481CrossRefPubMed
Metadata
Title
CT-defined phenotype of pulmonary artery stenoses in Alagille syndrome
Authors
Renee M. Rodriguez
Jeffrey A. Feinstein
Frandics P. Chan
Publication date
01-07-2016
Publisher
Springer Berlin Heidelberg
Published in
Pediatric Radiology / Issue 8/2016
Print ISSN: 0301-0449
Electronic ISSN: 1432-1998
DOI
https://doi.org/10.1007/s00247-016-3580-4

Other articles of this Issue 8/2016

Pediatric Radiology 8/2016 Go to the issue