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Disease recurrence after lung transplantation for idiopathic pulmonary hemosiderosis

Idiopathic pulmonary hemosiderosis is characterized by the triad of hemoptysis, iron deficiency anemia and pulmonary infiltrates. Though idiopathic pulmonary hemosiderosis has classically been described as a childhood disease, survival into adulthood is possible. Treatment options for advanced and/o...

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Detalles Bibliográficos
Autores principales: Ross, Bryan, Halloran, Kieran, Adam, Benjamin, Laing, Bryce, Hirji, Alim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7305376/
https://www.ncbi.nlm.nih.gov/pubmed/32577369
http://dx.doi.org/10.1016/j.rmcr.2020.101128
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author Ross, Bryan
Halloran, Kieran
Adam, Benjamin
Laing, Bryce
Hirji, Alim
author_facet Ross, Bryan
Halloran, Kieran
Adam, Benjamin
Laing, Bryce
Hirji, Alim
author_sort Ross, Bryan
collection PubMed
description Idiopathic pulmonary hemosiderosis is characterized by the triad of hemoptysis, iron deficiency anemia and pulmonary infiltrates. Though idiopathic pulmonary hemosiderosis has classically been described as a childhood disease, survival into adulthood is possible. Treatment options for advanced and/or refractory disease is limited, and in our unique case of idiopathic pulmonary hemosiderosis with precapillary pulmonary hypertension, lung transplantation has had a favorable short-term outcome. We also demonstrate that disease recurrence of idiopathic pulmonary hemosiderosis following lung transplantation is possible.
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spelling pubmed-73053762020-06-22 Disease recurrence after lung transplantation for idiopathic pulmonary hemosiderosis Ross, Bryan Halloran, Kieran Adam, Benjamin Laing, Bryce Hirji, Alim Respir Med Case Rep Case Report Idiopathic pulmonary hemosiderosis is characterized by the triad of hemoptysis, iron deficiency anemia and pulmonary infiltrates. Though idiopathic pulmonary hemosiderosis has classically been described as a childhood disease, survival into adulthood is possible. Treatment options for advanced and/or refractory disease is limited, and in our unique case of idiopathic pulmonary hemosiderosis with precapillary pulmonary hypertension, lung transplantation has had a favorable short-term outcome. We also demonstrate that disease recurrence of idiopathic pulmonary hemosiderosis following lung transplantation is possible. Elsevier 2020-06-10 /pmc/articles/PMC7305376/ /pubmed/32577369 http://dx.doi.org/10.1016/j.rmcr.2020.101128 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Ross, Bryan
Halloran, Kieran
Adam, Benjamin
Laing, Bryce
Hirji, Alim
Disease recurrence after lung transplantation for idiopathic pulmonary hemosiderosis
title Disease recurrence after lung transplantation for idiopathic pulmonary hemosiderosis
title_full Disease recurrence after lung transplantation for idiopathic pulmonary hemosiderosis
title_fullStr Disease recurrence after lung transplantation for idiopathic pulmonary hemosiderosis
title_full_unstemmed Disease recurrence after lung transplantation for idiopathic pulmonary hemosiderosis
title_short Disease recurrence after lung transplantation for idiopathic pulmonary hemosiderosis
title_sort disease recurrence after lung transplantation for idiopathic pulmonary hemosiderosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7305376/
https://www.ncbi.nlm.nih.gov/pubmed/32577369
http://dx.doi.org/10.1016/j.rmcr.2020.101128
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