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A case of invasive pulmonary aspergillosis during treatment for acute exacerbation of interstitial lung disease

Prolonged immunosuppressive therapy is a risk factor for invasive pulmonary aspergillosis. We report a case of a 79-yearold man who underwent immunosuppressive therapy with methylprednisolone and cyclosporine for an acute exacerbation of interstitial lung disease. Ten days after initiation of immuno...

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Detalles Bibliográficos
Autores principales: Ugajin, Motoi, Kani, Hisanori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315312/
https://www.ncbi.nlm.nih.gov/pubmed/30662692
http://dx.doi.org/10.4081/idr.2018.7785
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author Ugajin, Motoi
Kani, Hisanori
author_facet Ugajin, Motoi
Kani, Hisanori
author_sort Ugajin, Motoi
collection PubMed
description Prolonged immunosuppressive therapy is a risk factor for invasive pulmonary aspergillosis. We report a case of a 79-yearold man who underwent immunosuppressive therapy with methylprednisolone and cyclosporine for an acute exacerbation of interstitial lung disease. Ten days after initiation of immunosuppressive therapy, the patient reported night sweats and purulent sputum, and chest computed tomography scan revealed consolidation. He was diagnosed with invasive pulmonary aspergillosis, and required vasopressor support with oxygen therapy. After the administration of voriconazole and the modulation of immunosuppressive therapy, his condition improved. Short-term immunosuppressive therapy can also induce invasive pulmonary aspergillosis.
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spelling pubmed-63153122019-01-18 A case of invasive pulmonary aspergillosis during treatment for acute exacerbation of interstitial lung disease Ugajin, Motoi Kani, Hisanori Infect Dis Rep Case Report Prolonged immunosuppressive therapy is a risk factor for invasive pulmonary aspergillosis. We report a case of a 79-yearold man who underwent immunosuppressive therapy with methylprednisolone and cyclosporine for an acute exacerbation of interstitial lung disease. Ten days after initiation of immunosuppressive therapy, the patient reported night sweats and purulent sputum, and chest computed tomography scan revealed consolidation. He was diagnosed with invasive pulmonary aspergillosis, and required vasopressor support with oxygen therapy. After the administration of voriconazole and the modulation of immunosuppressive therapy, his condition improved. Short-term immunosuppressive therapy can also induce invasive pulmonary aspergillosis. PAGEPress Publications, Pavia, Italy 2018-12-05 /pmc/articles/PMC6315312/ /pubmed/30662692 http://dx.doi.org/10.4081/idr.2018.7785 Text en ©Copyright M. Ugajin and H. Kani, 2018 http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Case Report
Ugajin, Motoi
Kani, Hisanori
A case of invasive pulmonary aspergillosis during treatment for acute exacerbation of interstitial lung disease
title A case of invasive pulmonary aspergillosis during treatment for acute exacerbation of interstitial lung disease
title_full A case of invasive pulmonary aspergillosis during treatment for acute exacerbation of interstitial lung disease
title_fullStr A case of invasive pulmonary aspergillosis during treatment for acute exacerbation of interstitial lung disease
title_full_unstemmed A case of invasive pulmonary aspergillosis during treatment for acute exacerbation of interstitial lung disease
title_short A case of invasive pulmonary aspergillosis during treatment for acute exacerbation of interstitial lung disease
title_sort case of invasive pulmonary aspergillosis during treatment for acute exacerbation of interstitial lung disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315312/
https://www.ncbi.nlm.nih.gov/pubmed/30662692
http://dx.doi.org/10.4081/idr.2018.7785
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