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Alveolar Hemorrhage

Diffuse alveolar hemorrhage (DAH) is a life-threatening condition, characterized by extensive intra-alveolar hemorrhage. This condition can result from a variety of diseases such as vasculitis, primary systemic as well as secondary pulmonary hypertension, autoimmune diseases including collagen vascu...

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Detalles Bibliográficos
Autores principales: Popper, Helmut, Murer, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230147/
http://dx.doi.org/10.1007/978-3-030-22664-0_31
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author Popper, Helmut
Murer, Bruno
author_facet Popper, Helmut
Murer, Bruno
author_sort Popper, Helmut
collection PubMed
description Diffuse alveolar hemorrhage (DAH) is a life-threatening condition, characterized by extensive intra-alveolar hemorrhage. This condition can result from a variety of diseases such as vasculitis, primary systemic as well as secondary pulmonary hypertension, autoimmune diseases including collagen vascular diseases, Goodpasture syndrome, antiphospholipid autoantibody syndrome, infections such as tuberculosis, influenza virus, hantavirus, SARS, dengue fever, Nile virus fever, inhalation of herbicides and pesticides, drug reactions, especially cytostatics. Most cases of DAH are caused by capillaritis associated with systemic autoimmune diseases. In BAL specimen, there are red blood cells as well as hemosiderin-laden macrophages—it is essential to differentiate DAH from artificial bleeding induced by bronchoscopy or biopsy, as well as from aspiration from the upper respiratory tract. DAH may also occur as an idiopathic condition. It should be distinguished from focal pulmonary hemorrhage secondary to infections, arteriovenous malformation or pulmonary embolism. Early bronchoscopy with bronchoalveolar lavage is usually the first approach to exclude infections. Biopsy can help to identify the cause to direct the therapy.
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spelling pubmed-72301472020-05-18 Alveolar Hemorrhage Popper, Helmut Murer, Bruno Pulmonary Pathology Article Diffuse alveolar hemorrhage (DAH) is a life-threatening condition, characterized by extensive intra-alveolar hemorrhage. This condition can result from a variety of diseases such as vasculitis, primary systemic as well as secondary pulmonary hypertension, autoimmune diseases including collagen vascular diseases, Goodpasture syndrome, antiphospholipid autoantibody syndrome, infections such as tuberculosis, influenza virus, hantavirus, SARS, dengue fever, Nile virus fever, inhalation of herbicides and pesticides, drug reactions, especially cytostatics. Most cases of DAH are caused by capillaritis associated with systemic autoimmune diseases. In BAL specimen, there are red blood cells as well as hemosiderin-laden macrophages—it is essential to differentiate DAH from artificial bleeding induced by bronchoscopy or biopsy, as well as from aspiration from the upper respiratory tract. DAH may also occur as an idiopathic condition. It should be distinguished from focal pulmonary hemorrhage secondary to infections, arteriovenous malformation or pulmonary embolism. Early bronchoscopy with bronchoalveolar lavage is usually the first approach to exclude infections. Biopsy can help to identify the cause to direct the therapy. 2020-05-18 /pmc/articles/PMC7230147/ http://dx.doi.org/10.1007/978-3-030-22664-0_31 Text en © Springer Nature Switzerland AG 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Article
Popper, Helmut
Murer, Bruno
Alveolar Hemorrhage
title Alveolar Hemorrhage
title_full Alveolar Hemorrhage
title_fullStr Alveolar Hemorrhage
title_full_unstemmed Alveolar Hemorrhage
title_short Alveolar Hemorrhage
title_sort alveolar hemorrhage
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7230147/
http://dx.doi.org/10.1007/978-3-030-22664-0_31
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