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Peripheral pulmonary stenosis with Noonan syndrome treated by balloon pulmonary angioplasty

Noonan syndrome is known to have various cardiovascular defects, which include pulmonary artery stenosis. Pulmonary artery stenosis is characterized by obstruction of pulmonary artery blood flow that can cause elevated pulmonary artery pressure and ventilation-perfusion inequality, which can cause d...

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Autores principales: Ko, Seien, Komuro, Jin, Katsumata, Yoshinori, Shiraishi, Yasuyuki, Kawakami, Takashi, Yamada, Yoshitake, Yuasa, Shinsuke, Kohno, Takashi, Kosaki, Kenjiro, Fukuda, Keiichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7675873/
https://www.ncbi.nlm.nih.gov/pubmed/33240484
http://dx.doi.org/10.1177/2045894020954310
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author Ko, Seien
Komuro, Jin
Katsumata, Yoshinori
Shiraishi, Yasuyuki
Kawakami, Takashi
Yamada, Yoshitake
Yuasa, Shinsuke
Kohno, Takashi
Kosaki, Kenjiro
Fukuda, Keiichi
author_facet Ko, Seien
Komuro, Jin
Katsumata, Yoshinori
Shiraishi, Yasuyuki
Kawakami, Takashi
Yamada, Yoshitake
Yuasa, Shinsuke
Kohno, Takashi
Kosaki, Kenjiro
Fukuda, Keiichi
author_sort Ko, Seien
collection PubMed
description Noonan syndrome is known to have various cardiovascular defects, which include pulmonary artery stenosis. Pulmonary artery stenosis is characterized by obstruction of pulmonary artery blood flow that can cause elevated pulmonary artery pressure and ventilation-perfusion inequality, which can cause dyspnea on exertion and eventually, heart failure. Although the etiology of pulmonary artery stenosis related to congenital diseases is still unknown, balloon pulmonary angioplasty has being reported to be effective to selected patients with Alagille and Williams syndromes, but not from Noonan syndrome despite of modest prevalence of pulmonary artery stenosis. Here, we report the first Noonan syndrome patient with pulmonary artery stenosis who underwent successful balloon pulmonary angioplasty. The strategy used in balloon pulmonary angioplasty was planned with careful morphologic evaluation by computed tomographic angiography, and performed with scoring balloons in a graded approach with multiple sessions. After balloon pulmonary angioplasty, we confirmed maintained dilation of lesions and symptom alleviation, suggesting that balloon pulmonary angioplasty can be performed safely on pulmonary artery stenosis in a Noonan syndrome patient.
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spelling pubmed-76758732020-11-24 Peripheral pulmonary stenosis with Noonan syndrome treated by balloon pulmonary angioplasty Ko, Seien Komuro, Jin Katsumata, Yoshinori Shiraishi, Yasuyuki Kawakami, Takashi Yamada, Yoshitake Yuasa, Shinsuke Kohno, Takashi Kosaki, Kenjiro Fukuda, Keiichi Pulm Circ Case Report Noonan syndrome is known to have various cardiovascular defects, which include pulmonary artery stenosis. Pulmonary artery stenosis is characterized by obstruction of pulmonary artery blood flow that can cause elevated pulmonary artery pressure and ventilation-perfusion inequality, which can cause dyspnea on exertion and eventually, heart failure. Although the etiology of pulmonary artery stenosis related to congenital diseases is still unknown, balloon pulmonary angioplasty has being reported to be effective to selected patients with Alagille and Williams syndromes, but not from Noonan syndrome despite of modest prevalence of pulmonary artery stenosis. Here, we report the first Noonan syndrome patient with pulmonary artery stenosis who underwent successful balloon pulmonary angioplasty. The strategy used in balloon pulmonary angioplasty was planned with careful morphologic evaluation by computed tomographic angiography, and performed with scoring balloons in a graded approach with multiple sessions. After balloon pulmonary angioplasty, we confirmed maintained dilation of lesions and symptom alleviation, suggesting that balloon pulmonary angioplasty can be performed safely on pulmonary artery stenosis in a Noonan syndrome patient. SAGE Publications 2020-11-10 /pmc/articles/PMC7675873/ /pubmed/33240484 http://dx.doi.org/10.1177/2045894020954310 Text en © The Author(s) 2020 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
Ko, Seien
Komuro, Jin
Katsumata, Yoshinori
Shiraishi, Yasuyuki
Kawakami, Takashi
Yamada, Yoshitake
Yuasa, Shinsuke
Kohno, Takashi
Kosaki, Kenjiro
Fukuda, Keiichi
Peripheral pulmonary stenosis with Noonan syndrome treated by balloon pulmonary angioplasty
title Peripheral pulmonary stenosis with Noonan syndrome treated by balloon pulmonary angioplasty
title_full Peripheral pulmonary stenosis with Noonan syndrome treated by balloon pulmonary angioplasty
title_fullStr Peripheral pulmonary stenosis with Noonan syndrome treated by balloon pulmonary angioplasty
title_full_unstemmed Peripheral pulmonary stenosis with Noonan syndrome treated by balloon pulmonary angioplasty
title_short Peripheral pulmonary stenosis with Noonan syndrome treated by balloon pulmonary angioplasty
title_sort peripheral pulmonary stenosis with noonan syndrome treated by balloon pulmonary angioplasty
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7675873/
https://www.ncbi.nlm.nih.gov/pubmed/33240484
http://dx.doi.org/10.1177/2045894020954310
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