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Magnetic resonance lymphangiography in group 1 paediatric pulmonary arterial hypertension

Pulmonary hypertension could have thoracic lymphatic abnormalities caused by right ventricular failure. Since there is no description of such abnormalities, the purpose of this study was to investigate them with magnetic resonance. Prospective review magnetic resonance T2-weighted lymphangiography w...

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Autores principales: Juaneda, Ernesto, Catalfamo, Danilo, Fregapani, Juan P., Peirone, Alejandro, Juaneda, Ignacio, Kreutzer, Cristian, Lucino, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020108/
https://www.ncbi.nlm.nih.gov/pubmed/33868641
http://dx.doi.org/10.1177/20458940211004777
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author Juaneda, Ernesto
Catalfamo, Danilo
Fregapani, Juan P.
Peirone, Alejandro
Juaneda, Ignacio
Kreutzer, Cristian
Lucino, Sergio
author_facet Juaneda, Ernesto
Catalfamo, Danilo
Fregapani, Juan P.
Peirone, Alejandro
Juaneda, Ignacio
Kreutzer, Cristian
Lucino, Sergio
author_sort Juaneda, Ernesto
collection PubMed
description Pulmonary hypertension could have thoracic lymphatic abnormalities caused by right ventricular failure. Since there is no description of such abnormalities, the purpose of this study was to investigate them with magnetic resonance. Prospective review magnetic resonance T2-weighted lymphangiography was performed between January 2017 and October 2019 through quantitative thoracic duct diameter, diameter index and qualitative lymphatic abnormalities types: 1 – little or none abnormalities, 2 – abnormalities in supraclavicular region, 3 – abnormalities extending into the mediastinum and 4 – abnormalities extending into the lung. Five patients with group 1 pulmonary arterial hypertension participated in this study. The mean age was 12.44 ± 4.92 years, three male and two female. The quantitative analysis yielded the following results: mean thoracic duct diameter of 2.92 ± 0.16 mm and thoracic duct index 2.28 ± 1.03 mm/m(2). Qualitative lymphangiography abnormalities were type 1 in three patients, type 2 in one, all with low-risk determinants, and type 3 in one with high-risk determinants and right ventricular failure. Magnetic resonance T2-weighted lymphangiography in group 1 paediatric pulmonary arterial hypertension allowed for the identification of the thoracic duct, which was used to perform both quantitative and qualitative analysis of thoracic lymphatic abnormalities, in particular when increased high-risk determinants and right ventricular failure were present. These features represent an extracardiac finding useful to understand systemic venous congestion impact on lymphatic system.
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spelling pubmed-80201082021-04-16 Magnetic resonance lymphangiography in group 1 paediatric pulmonary arterial hypertension Juaneda, Ernesto Catalfamo, Danilo Fregapani, Juan P. Peirone, Alejandro Juaneda, Ignacio Kreutzer, Cristian Lucino, Sergio Pulm Circ Case Report Pulmonary hypertension could have thoracic lymphatic abnormalities caused by right ventricular failure. Since there is no description of such abnormalities, the purpose of this study was to investigate them with magnetic resonance. Prospective review magnetic resonance T2-weighted lymphangiography was performed between January 2017 and October 2019 through quantitative thoracic duct diameter, diameter index and qualitative lymphatic abnormalities types: 1 – little or none abnormalities, 2 – abnormalities in supraclavicular region, 3 – abnormalities extending into the mediastinum and 4 – abnormalities extending into the lung. Five patients with group 1 pulmonary arterial hypertension participated in this study. The mean age was 12.44 ± 4.92 years, three male and two female. The quantitative analysis yielded the following results: mean thoracic duct diameter of 2.92 ± 0.16 mm and thoracic duct index 2.28 ± 1.03 mm/m(2). Qualitative lymphangiography abnormalities were type 1 in three patients, type 2 in one, all with low-risk determinants, and type 3 in one with high-risk determinants and right ventricular failure. Magnetic resonance T2-weighted lymphangiography in group 1 paediatric pulmonary arterial hypertension allowed for the identification of the thoracic duct, which was used to perform both quantitative and qualitative analysis of thoracic lymphatic abnormalities, in particular when increased high-risk determinants and right ventricular failure were present. These features represent an extracardiac finding useful to understand systemic venous congestion impact on lymphatic system. SAGE Publications 2021-03-30 /pmc/articles/PMC8020108/ /pubmed/33868641 http://dx.doi.org/10.1177/20458940211004777 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Case Report
Juaneda, Ernesto
Catalfamo, Danilo
Fregapani, Juan P.
Peirone, Alejandro
Juaneda, Ignacio
Kreutzer, Cristian
Lucino, Sergio
Magnetic resonance lymphangiography in group 1 paediatric pulmonary arterial hypertension
title Magnetic resonance lymphangiography in group 1 paediatric pulmonary arterial hypertension
title_full Magnetic resonance lymphangiography in group 1 paediatric pulmonary arterial hypertension
title_fullStr Magnetic resonance lymphangiography in group 1 paediatric pulmonary arterial hypertension
title_full_unstemmed Magnetic resonance lymphangiography in group 1 paediatric pulmonary arterial hypertension
title_short Magnetic resonance lymphangiography in group 1 paediatric pulmonary arterial hypertension
title_sort magnetic resonance lymphangiography in group 1 paediatric pulmonary arterial hypertension
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020108/
https://www.ncbi.nlm.nih.gov/pubmed/33868641
http://dx.doi.org/10.1177/20458940211004777
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