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Isolated unilateral pulmonary vein atresia with hemoptysis in a child: A case report and literature review

RATIONALE: Hemoptysis is an uncommon chief complaint but a distressing symptom in pediatric patients. Due to the recurrence and mortality in minor patients, an accurate diagnosis of the underlying cause is quite essential for treatment. The etiologies causing hemoptysis in children are similar to th...

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Autores principales: Tang, Changqing, Duan, Hongyu, Zhou, Kaiyu, Hua, Yimin, Liu, Xiaoliang, Li, Yifei, Wang, Chuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112952/
https://www.ncbi.nlm.nih.gov/pubmed/30142786
http://dx.doi.org/10.1097/MD.0000000000011882
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author Tang, Changqing
Duan, Hongyu
Zhou, Kaiyu
Hua, Yimin
Liu, Xiaoliang
Li, Yifei
Wang, Chuan
author_facet Tang, Changqing
Duan, Hongyu
Zhou, Kaiyu
Hua, Yimin
Liu, Xiaoliang
Li, Yifei
Wang, Chuan
author_sort Tang, Changqing
collection PubMed
description RATIONALE: Hemoptysis is an uncommon chief complaint but a distressing symptom in pediatric patients. Due to the recurrence and mortality in minor patients, an accurate diagnosis of the underlying cause is quite essential for treatment. The etiologies causing hemoptysis in children are similar to that in adults. Isolated unilateral pulmonary vein atresia (PVA), as an unusual cardiovascular anomaly, has rarely been reported to be an etiology of hemoptysis in children. PATIENT CONCERNS: A 2-year and 11-month-old boy was admitted into our hospital with a complaint of recurrent hemoptysis for 2 months and the symptom became more aggravated in recent 4 days before admission. Physical examination was only remarkable for slightly diminished breath sounds over the left lung field, pale face, and colorless lip. Series of targeted laboratory evaluation were negative expect for anemia. Due to the identification of asymmetrical transparency of bilateral lung, slight emphysema of right lung, less volume of left lung with ground-glass opacity and reticular opacity, and ipsilateral mediastinal shift on chest CT, and varices of submucosal vessels in the left bronchial tree on the fiber-optic bronchoscope. DIAGNOSES: It more likely indicated a congenital cardiovascular disease. The diagnosis of left isolated unilateral PVA was ultimately confirmed through chest CT angiography (CTA) with three-dimensional (3D) reconstruction. INTERVENTIONS: Since the boy did not complain with hemoptysis after admission, respiratory tract infections seldom occurred and no pulmonary hypertension was detected, a conservative approach was chosen with periodic clinical follow-up after discussing with the cardiac surgeons and in accordance to his parents’ own wishes. OUTCOMES: Fortunately, he was doing well after 3 months of clinical observation. LESSONS: We firstly reported a rare case of hemoptysis in children secondary to isolated unilateral PVA with no associated congenital heart disease in Chinese population. It is significant to improve the recognition and prompt diagnosis of this rare condition for pediatric clinicians, and widen the etiology spectrum of hemoptysis in children. The diagnosis of unilateral PVA should be considered for a patient with recurrent hemoptysis and imaging findings that indicate hypoplastic lung, ipsilateral mediastinal shift, and smooth margins of left atrium without evidence of rudimentary pulmonary veins.
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spelling pubmed-61129522018-09-07 Isolated unilateral pulmonary vein atresia with hemoptysis in a child: A case report and literature review Tang, Changqing Duan, Hongyu Zhou, Kaiyu Hua, Yimin Liu, Xiaoliang Li, Yifei Wang, Chuan Medicine (Baltimore) Research Article RATIONALE: Hemoptysis is an uncommon chief complaint but a distressing symptom in pediatric patients. Due to the recurrence and mortality in minor patients, an accurate diagnosis of the underlying cause is quite essential for treatment. The etiologies causing hemoptysis in children are similar to that in adults. Isolated unilateral pulmonary vein atresia (PVA), as an unusual cardiovascular anomaly, has rarely been reported to be an etiology of hemoptysis in children. PATIENT CONCERNS: A 2-year and 11-month-old boy was admitted into our hospital with a complaint of recurrent hemoptysis for 2 months and the symptom became more aggravated in recent 4 days before admission. Physical examination was only remarkable for slightly diminished breath sounds over the left lung field, pale face, and colorless lip. Series of targeted laboratory evaluation were negative expect for anemia. Due to the identification of asymmetrical transparency of bilateral lung, slight emphysema of right lung, less volume of left lung with ground-glass opacity and reticular opacity, and ipsilateral mediastinal shift on chest CT, and varices of submucosal vessels in the left bronchial tree on the fiber-optic bronchoscope. DIAGNOSES: It more likely indicated a congenital cardiovascular disease. The diagnosis of left isolated unilateral PVA was ultimately confirmed through chest CT angiography (CTA) with three-dimensional (3D) reconstruction. INTERVENTIONS: Since the boy did not complain with hemoptysis after admission, respiratory tract infections seldom occurred and no pulmonary hypertension was detected, a conservative approach was chosen with periodic clinical follow-up after discussing with the cardiac surgeons and in accordance to his parents’ own wishes. OUTCOMES: Fortunately, he was doing well after 3 months of clinical observation. LESSONS: We firstly reported a rare case of hemoptysis in children secondary to isolated unilateral PVA with no associated congenital heart disease in Chinese population. It is significant to improve the recognition and prompt diagnosis of this rare condition for pediatric clinicians, and widen the etiology spectrum of hemoptysis in children. The diagnosis of unilateral PVA should be considered for a patient with recurrent hemoptysis and imaging findings that indicate hypoplastic lung, ipsilateral mediastinal shift, and smooth margins of left atrium without evidence of rudimentary pulmonary veins. Wolters Kluwer Health 2018-08-24 /pmc/articles/PMC6112952/ /pubmed/30142786 http://dx.doi.org/10.1097/MD.0000000000011882 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0.
spellingShingle Research Article
Tang, Changqing
Duan, Hongyu
Zhou, Kaiyu
Hua, Yimin
Liu, Xiaoliang
Li, Yifei
Wang, Chuan
Isolated unilateral pulmonary vein atresia with hemoptysis in a child: A case report and literature review
title Isolated unilateral pulmonary vein atresia with hemoptysis in a child: A case report and literature review
title_full Isolated unilateral pulmonary vein atresia with hemoptysis in a child: A case report and literature review
title_fullStr Isolated unilateral pulmonary vein atresia with hemoptysis in a child: A case report and literature review
title_full_unstemmed Isolated unilateral pulmonary vein atresia with hemoptysis in a child: A case report and literature review
title_short Isolated unilateral pulmonary vein atresia with hemoptysis in a child: A case report and literature review
title_sort isolated unilateral pulmonary vein atresia with hemoptysis in a child: a case report and literature review
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112952/
https://www.ncbi.nlm.nih.gov/pubmed/30142786
http://dx.doi.org/10.1097/MD.0000000000011882
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