Abstract
We aimed to assess the frequency of criss-cross pulmonary arteries and associated intracardiac and vascular anomalies in patients who underwent CT angiography due to suspected congenital heart disease or vascular anomaly at our hospital. We retrospectively evaluated the CT angiography images of 355 patients aged 0–18 years between April 2018 and December 2022. The presence of the criss-cross pulmonary artery anomaly was assessed. Additionally, in patients with a criss-cross pulmonary artery anomaly, accompanying branch pulmonary artery anomalies, aortic arch anomalies, and other vascular-cardiac anomalies were also evaluated. A total of 331 patients’ images were evaluated. Criss-cross pulmonary artery anomaly was present in 57 patients (17.2%). Pulmonary artery branch anomaly was present in 16, aortic arch anomaly in 40 patients (70%) with criss-cross pulmonary artery anomaly, while associated intracardiac pathology (by echocardiography) was detected in 43 patients (75.4%). The frequency of criss-cross pulmonary artery was found to be significantly higher in patients with any aortic arch anomaly (p = 0.01). This study represents one of the largest series of patients with criss-cross pulmonary artery anomalies. Our results suggests that it may be more common than previously recognized and potentially overlooked. It is crucial to consider the presence of this anomaly in patients with complex aortic arch anomalies or cardiac pathologies, as it may have implications for surgical approaches and potential complications. Increased awareness of this anomaly among cardiologists and radiologists is necessary for accurate diagnosis and appropriate management.
Similar content being viewed by others
References
Newman B, Alkhori N (2020) Congenital central pulmonary artery anomalies: part 1. Pediatr Radiol 50(8):1022–1029
Newman B, Alkhori N (2020) Congenital central pulmonary artery anomalies: part 2. Pediatr Radiol 50(8):1030–1040
Vaz A, Maffezzolli PB, Pedrazzani BM (2021) Anomalous origin with and without crossing of the pulmonary arteries. Pediatr Radiol 51(8):1541–1543
Recto MR, Parness IA, Gelb BD, Lopez L, Lai WW (1997) Clinical implications and possible association of malposition of the branch pulmonary arteries with DiGeorge syndrome and microdeletion of chromosomal region 22q11. Am J Cardiol 80(12):1624–1627
Aeba R, Kotani S, Yamabe K, Yozu R (2013) Bilateral banding of malpositioned pulmonary artery branches. Pediatr Cardiol 34:1938–1940
Said SM, Hoggard E, Narasimhan S (2023) Surgical experience with crossed and anomalous origin of the pulmonary arteries from the pulmonary trunk: a single center report of 24 cases. World J Pediatr Congenit Heart Surg 14(2):185–193
Mastromoro G, Calcagni G, Vignaroli W, Anaclerio S, Pugnaloni F, Rinelli G et al (2022) Crossed pulmonary arteries: an underestimated cardiovascular variant with a strong association with genetic syndromes—a report of 74 cases with systematic review of the literature. Am J Med Genet A 188(8):2351–2359
Agarwal A, Arulselvam V, Al Amer SR, Kalis NN (2021) Crossed pulmonary arteries: a literature review. J Indian Acad Echocardiogr Cardiovasc Imaging 5(3):207
Babaoğlu K, Altun G, Binnetoğlu K, Dönmez M, Kayabey Ö, Anık Y (2013) Crossed pulmonary arteries: a report on 20 cases with an emphasis on the clinical features and the genetic and cardiac abnormalities. Pediatr Cardiol 34:1785–1790
Jue KL, Lockman LA, Edwards JE (1966) Anomalous origins of pulmonary arteries from pulmonary frunk (“crossed pulmonary arteries”): observation in a case with 18 trisomy syndrome. Am Heart J 71(6):807–812
Verma M, Pandey NN, Nagulakonda S, Kumar S, Ramakrishnan S (2022) Evaluation of cardiovascular morphology and associated anomalies in patients with crossed pulmonary arteries on multidetector computed tomography angiography. J Card Surg 37(8):2278–2284
Zhang J, Gao Y, Huang G, Hu X, Yang J, Ma X (2018) The role of echocardiography in diagnosing crossed pulmonary arteries. J Cardiol Diagn Res 1:3–9
Mastromoro G, Calcagni G, Versacci P, Putotto C, Chinali M, Lambiase C et al (2019) Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice. PLoS One 14(4):e0211170
Korpaisarn S, Trachoo O, Sriphrapradang C (2013) Chromosome 22q11.2 deletion syndrome presenting as adult onset hypoparathyroidism: clues to diagnosis from dysmorphic facial features. Case Rep Endocrinol 2013:802793
Funding
The authors declare that no funds, grants, or other support were received during the preparation of this manuscript.
Author information
Authors and Affiliations
Contributions
All authors contributed to the study conception and design. Material preparation, data collection, and analysis were performed by DB, YND, and UYU. The first draft of the manuscript was written by DB and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Conflict of interest
The authors have no relevant financial or non-financial interests to disclose.
Ethical Approval
This study was performed in line with the principles of the Declaration of Helsinki. Approval for this study was obtained from Van Regional Training and Research Hospital, on 01/04/2023; approval number: 2023/01-09.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Bako, D., Dönmez, Y.N., Uncu, U.Y. et al. Cross or Not to Cross-Dilemma of the Pulmonary Arteries. Pediatr Cardiol (2023). https://doi.org/10.1007/s00246-023-03393-6
Received:
Accepted:
Published:
DOI: https://doi.org/10.1007/s00246-023-03393-6