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Pulmonary capillary haemangiomatosis – An unusual cause of hypoxia
We describe the case of a 58-year-old man who presented with progressive dyspnoea on exertion and severe exertional hypoxia. There was a paucity of radiological findings, mild pulmonary hypertension, and no demonstrable anatomical shunt. Post mortem examination of lung tissue suggested a diagnosis o...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920353/ https://www.ncbi.nlm.nih.gov/pubmed/26029600 http://dx.doi.org/10.1016/j.rmcr.2012.09.001 |
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author | Aston, Kerry Riddell, Gareth J. Sheppard, Mary N. Wells, Athol U. Riley, Marshall S. |
author_facet | Aston, Kerry Riddell, Gareth J. Sheppard, Mary N. Wells, Athol U. Riley, Marshall S. |
author_sort | Aston, Kerry |
collection | PubMed |
description | We describe the case of a 58-year-old man who presented with progressive dyspnoea on exertion and severe exertional hypoxia. There was a paucity of radiological findings, mild pulmonary hypertension, and no demonstrable anatomical shunt. Post mortem examination of lung tissue suggested a diagnosis of pulmonary capillary haemangiomatosis. The case is unusual in displaying few radiological findings. We postulate that the severe hypoxia was due to shunting through the abnormal capillary proliferations. |
format | Online Article Text |
id | pubmed-3920353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-39203532014-10-15 Pulmonary capillary haemangiomatosis – An unusual cause of hypoxia Aston, Kerry Riddell, Gareth J. Sheppard, Mary N. Wells, Athol U. Riley, Marshall S. Respir Med Case Rep Case Report We describe the case of a 58-year-old man who presented with progressive dyspnoea on exertion and severe exertional hypoxia. There was a paucity of radiological findings, mild pulmonary hypertension, and no demonstrable anatomical shunt. Post mortem examination of lung tissue suggested a diagnosis of pulmonary capillary haemangiomatosis. The case is unusual in displaying few radiological findings. We postulate that the severe hypoxia was due to shunting through the abnormal capillary proliferations. Elsevier 2012-11-08 /pmc/articles/PMC3920353/ /pubmed/26029600 http://dx.doi.org/10.1016/j.rmcr.2012.09.001 Text en © 2012 Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Case Report Aston, Kerry Riddell, Gareth J. Sheppard, Mary N. Wells, Athol U. Riley, Marshall S. Pulmonary capillary haemangiomatosis – An unusual cause of hypoxia |
title | Pulmonary capillary haemangiomatosis – An unusual cause of hypoxia |
title_full | Pulmonary capillary haemangiomatosis – An unusual cause of hypoxia |
title_fullStr | Pulmonary capillary haemangiomatosis – An unusual cause of hypoxia |
title_full_unstemmed | Pulmonary capillary haemangiomatosis – An unusual cause of hypoxia |
title_short | Pulmonary capillary haemangiomatosis – An unusual cause of hypoxia |
title_sort | pulmonary capillary haemangiomatosis – an unusual cause of hypoxia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920353/ https://www.ncbi.nlm.nih.gov/pubmed/26029600 http://dx.doi.org/10.1016/j.rmcr.2012.09.001 |
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