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Anomalous origin of the fetal pulmonary artery

OBJECTIVES: This study aims to investigate the efficacy of prenatal ultrasonography in diagnosing the anomalous origin of the fetal pulmonary artery (AOFPA). METHODS: A total of 26 AOFPA cases were retrospectively analyzed from January 2014 to January 2023. The features of the AOFPA were characteriz...

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Autores principales: Huang, Qiong, Ling, Wen, Wu, Qiumei, Guo, Shan, Dang, Tingting, Ma, Hong, Huang, Biying, Chen, Chunxia, Liu, Min, Qiu, Xiuqing, Weng, Zongjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338927/
https://www.ncbi.nlm.nih.gov/pubmed/37456564
http://dx.doi.org/10.3389/fped.2023.1204070
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author Huang, Qiong
Ling, Wen
Wu, Qiumei
Guo, Shan
Dang, Tingting
Ma, Hong
Huang, Biying
Chen, Chunxia
Liu, Min
Qiu, Xiuqing
Weng, Zongjie
author_facet Huang, Qiong
Ling, Wen
Wu, Qiumei
Guo, Shan
Dang, Tingting
Ma, Hong
Huang, Biying
Chen, Chunxia
Liu, Min
Qiu, Xiuqing
Weng, Zongjie
author_sort Huang, Qiong
collection PubMed
description OBJECTIVES: This study aims to investigate the efficacy of prenatal ultrasonography in diagnosing the anomalous origin of the fetal pulmonary artery (AOFPA). METHODS: A total of 26 AOFPA cases were retrospectively analyzed from January 2014 to January 2023. The features of the AOFPA were characterized by comparing the prenatal ultrasonic data with the results of anatomical casting after pregnancy termination or postnatal imaging and surgical intervention. Missed diagnoses and misdiagnoses were expounded. RESULTS: Of the 26 AOFPA cases, there were 13 cases of pulmonary artery sling, 8 cases of anomalous origin of the unilateral pulmonary artery, and five cases of unilateral absence of the pulmonary artery; 17 cases received pathological anatomy and casting after pregnancy termination, and nine cases were confirmed by postnatal imaging and surgery. Nineteen cases were accurately prenatally diagnosed (19/26, 73.1%), and seven cases were missed or misdiagnosed (7/26, 26.9%). CONCLUSIONS: Prenatal ultrasonography has a favorable diagnostic efficacy for anomalous origin of the fetal pulmonary artery. The absence of either the left or right pulmonary artery from the image of pulmonary artery bifurcation may indicate origin abnormalities of the pulmonary artery in fetuses, which signifies the necessity to detect the abnormal origin of the pulmonary artery on the affected side and other potential intracardiac malformation complications.
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spelling pubmed-103389272023-07-14 Anomalous origin of the fetal pulmonary artery Huang, Qiong Ling, Wen Wu, Qiumei Guo, Shan Dang, Tingting Ma, Hong Huang, Biying Chen, Chunxia Liu, Min Qiu, Xiuqing Weng, Zongjie Front Pediatr Pediatrics OBJECTIVES: This study aims to investigate the efficacy of prenatal ultrasonography in diagnosing the anomalous origin of the fetal pulmonary artery (AOFPA). METHODS: A total of 26 AOFPA cases were retrospectively analyzed from January 2014 to January 2023. The features of the AOFPA were characterized by comparing the prenatal ultrasonic data with the results of anatomical casting after pregnancy termination or postnatal imaging and surgical intervention. Missed diagnoses and misdiagnoses were expounded. RESULTS: Of the 26 AOFPA cases, there were 13 cases of pulmonary artery sling, 8 cases of anomalous origin of the unilateral pulmonary artery, and five cases of unilateral absence of the pulmonary artery; 17 cases received pathological anatomy and casting after pregnancy termination, and nine cases were confirmed by postnatal imaging and surgery. Nineteen cases were accurately prenatally diagnosed (19/26, 73.1%), and seven cases were missed or misdiagnosed (7/26, 26.9%). CONCLUSIONS: Prenatal ultrasonography has a favorable diagnostic efficacy for anomalous origin of the fetal pulmonary artery. The absence of either the left or right pulmonary artery from the image of pulmonary artery bifurcation may indicate origin abnormalities of the pulmonary artery in fetuses, which signifies the necessity to detect the abnormal origin of the pulmonary artery on the affected side and other potential intracardiac malformation complications. Frontiers Media S.A. 2023-06-29 /pmc/articles/PMC10338927/ /pubmed/37456564 http://dx.doi.org/10.3389/fped.2023.1204070 Text en © 2023 Huang, Ling, Wu, Guo, Dang, Ma, Huang, Chen, Liu, Qiu and Weng. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Huang, Qiong
Ling, Wen
Wu, Qiumei
Guo, Shan
Dang, Tingting
Ma, Hong
Huang, Biying
Chen, Chunxia
Liu, Min
Qiu, Xiuqing
Weng, Zongjie
Anomalous origin of the fetal pulmonary artery
title Anomalous origin of the fetal pulmonary artery
title_full Anomalous origin of the fetal pulmonary artery
title_fullStr Anomalous origin of the fetal pulmonary artery
title_full_unstemmed Anomalous origin of the fetal pulmonary artery
title_short Anomalous origin of the fetal pulmonary artery
title_sort anomalous origin of the fetal pulmonary artery
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338927/
https://www.ncbi.nlm.nih.gov/pubmed/37456564
http://dx.doi.org/10.3389/fped.2023.1204070
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