A Case of Bilateral Spontaneous Chylothorax with Respiratory Syncytial Virus Bronchiolitis

A case of bilateral spontaneous chylothorax with respiratory syncytial virus (RSV) bronchiolitis has never been reported. We report the case of a 7-month-old boy born at 33 weeks gestation with a history of Down syndrome, atrial septal defect, pulmonary hypertension, and chronic lung disease, hospit...

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Main Authors: Mario Briceno-Medina, Michael Perez, Jie Zhang, Ronak Naik, Samir Shah, Dai Kimura
Format: Article
Language:English
Published: Hindawi Limited 2019-01-01
Series:Case Reports in Pediatrics
Online Access:http://dx.doi.org/10.1155/2019/2853632
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spelling doaj-0e52d75c21854fe188f9aba38e0cd2a42020-11-24T22:26:24ZengHindawi LimitedCase Reports in Pediatrics2090-68032090-68112019-01-01201910.1155/2019/28536322853632A Case of Bilateral Spontaneous Chylothorax with Respiratory Syncytial Virus BronchiolitisMario Briceno-Medina0Michael Perez1Jie Zhang2Ronak Naik3Samir Shah4Dai Kimura5Division of Cardiology, Le Bonheur Children’s Hospital, University of Tennessee Health Science Center, Memphis, TN, USADivision of Cardiology, Le Bonheur Children’s Hospital, University of Tennessee Health Science Center, Memphis, TN, USADepartment of Pathology, Le Bonheur Children’s Hospital, University of Tennessee Health Science Center, Memphis, TN, USADivision of Cardiology, Le Bonheur Children’s Hospital, University of Tennessee Health Science Center, Memphis, TN, USADivision of Critical Care Medicine, Le Bonheur Children’s Hospital, University of Tennessee Health Science Center, Memphis, TN, USADivision of Critical Care Medicine, Le Bonheur Children’s Hospital, University of Tennessee Health Science Center, Memphis, TN, USAA case of bilateral spontaneous chylothorax with respiratory syncytial virus (RSV) bronchiolitis has never been reported. We report the case of a 7-month-old boy born at 33 weeks gestation with a history of Down syndrome, atrial septal defect, pulmonary hypertension, and chronic lung disease, hospitalized due to RSV bronchiolitis who developed bilateral spontaneous chylothorax with exacerbation of pulmonary hypertension (PH). The patient died after 9 weeks of mechanical ventilation and treatment for PH. The autopsy showed acute infectious signs, a chronic interstitial lung disease with pulmonary hypertensive changes and subpleural cysts with no evidence of congenital lymphangiectasia. The cause of chylothorax in this child could be multifactorial. However, worsening pulmonary hypertension with RSV infection might have partially contributed to the development of chylothorax through elevated superior venous cava pressure. Thoracentesis should be considered for patients with Down syndrome and PH associated with congenital heart disease who develop persistent pleural effusion during RSV bronchiolitis to rule out chylothorax.http://dx.doi.org/10.1155/2019/2853632
collection DOAJ
language English
format Article
sources DOAJ
author Mario Briceno-Medina
Michael Perez
Jie Zhang
Ronak Naik
Samir Shah
Dai Kimura
spellingShingle Mario Briceno-Medina
Michael Perez
Jie Zhang
Ronak Naik
Samir Shah
Dai Kimura
A Case of Bilateral Spontaneous Chylothorax with Respiratory Syncytial Virus Bronchiolitis
Case Reports in Pediatrics
author_facet Mario Briceno-Medina
Michael Perez
Jie Zhang
Ronak Naik
Samir Shah
Dai Kimura
author_sort Mario Briceno-Medina
title A Case of Bilateral Spontaneous Chylothorax with Respiratory Syncytial Virus Bronchiolitis
title_short A Case of Bilateral Spontaneous Chylothorax with Respiratory Syncytial Virus Bronchiolitis
title_full A Case of Bilateral Spontaneous Chylothorax with Respiratory Syncytial Virus Bronchiolitis
title_fullStr A Case of Bilateral Spontaneous Chylothorax with Respiratory Syncytial Virus Bronchiolitis
title_full_unstemmed A Case of Bilateral Spontaneous Chylothorax with Respiratory Syncytial Virus Bronchiolitis
title_sort case of bilateral spontaneous chylothorax with respiratory syncytial virus bronchiolitis
publisher Hindawi Limited
series Case Reports in Pediatrics
issn 2090-6803
2090-6811
publishDate 2019-01-01
description A case of bilateral spontaneous chylothorax with respiratory syncytial virus (RSV) bronchiolitis has never been reported. We report the case of a 7-month-old boy born at 33 weeks gestation with a history of Down syndrome, atrial septal defect, pulmonary hypertension, and chronic lung disease, hospitalized due to RSV bronchiolitis who developed bilateral spontaneous chylothorax with exacerbation of pulmonary hypertension (PH). The patient died after 9 weeks of mechanical ventilation and treatment for PH. The autopsy showed acute infectious signs, a chronic interstitial lung disease with pulmonary hypertensive changes and subpleural cysts with no evidence of congenital lymphangiectasia. The cause of chylothorax in this child could be multifactorial. However, worsening pulmonary hypertension with RSV infection might have partially contributed to the development of chylothorax through elevated superior venous cava pressure. Thoracentesis should be considered for patients with Down syndrome and PH associated with congenital heart disease who develop persistent pleural effusion during RSV bronchiolitis to rule out chylothorax.
url http://dx.doi.org/10.1155/2019/2853632
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