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Recurrent pneumothorax related to diffuse dendriform pulmonary ossification in genetically predisposed individual
Diffuse pulmonary ossification (DPO) is a rare disease with unknown pathogenesis, clinical manifestations, and treatment options. This report describes the diagnosis of DPO in an otherwise healthy 26‐year‐old man with recurrent spontaneous pneumothorax. His father was diagnosed with a similar lung c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155673/ https://www.ncbi.nlm.nih.gov/pubmed/27999676 http://dx.doi.org/10.1002/rcr2.211 |
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author | Tsai, Amy Po Yu English, John C. Murphy, Darra Sin, Don D. |
author_facet | Tsai, Amy Po Yu English, John C. Murphy, Darra Sin, Don D. |
author_sort | Tsai, Amy Po Yu |
collection | PubMed |
description | Diffuse pulmonary ossification (DPO) is a rare disease with unknown pathogenesis, clinical manifestations, and treatment options. This report describes the diagnosis of DPO in an otherwise healthy 26‐year‐old man with recurrent spontaneous pneumothorax. His father was diagnosed with a similar lung condition in his 30's with computed tomography (CT) images that were strikingly similar to those of the patient. This report suggests that DPO can induce spontaneous pneumothorax and its pathogenesis may have a possible genetic predisposition that needs further research. |
format | Online Article Text |
id | pubmed-5155673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-51556732016-12-20 Recurrent pneumothorax related to diffuse dendriform pulmonary ossification in genetically predisposed individual Tsai, Amy Po Yu English, John C. Murphy, Darra Sin, Don D. Respirol Case Rep Case Reports Diffuse pulmonary ossification (DPO) is a rare disease with unknown pathogenesis, clinical manifestations, and treatment options. This report describes the diagnosis of DPO in an otherwise healthy 26‐year‐old man with recurrent spontaneous pneumothorax. His father was diagnosed with a similar lung condition in his 30's with computed tomography (CT) images that were strikingly similar to those of the patient. This report suggests that DPO can induce spontaneous pneumothorax and its pathogenesis may have a possible genetic predisposition that needs further research. John Wiley & Sons, Ltd 2016-12-14 /pmc/articles/PMC5155673/ /pubmed/27999676 http://dx.doi.org/10.1002/rcr2.211 Text en © 2016 The Authors. Respirology Case Reports published by John Wiley & Sons Australia, Ltd on behalf of The Asian Pacific Society of Respirology This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Case Reports Tsai, Amy Po Yu English, John C. Murphy, Darra Sin, Don D. Recurrent pneumothorax related to diffuse dendriform pulmonary ossification in genetically predisposed individual |
title | Recurrent pneumothorax related to diffuse dendriform pulmonary ossification in genetically predisposed individual |
title_full | Recurrent pneumothorax related to diffuse dendriform pulmonary ossification in genetically predisposed individual |
title_fullStr | Recurrent pneumothorax related to diffuse dendriform pulmonary ossification in genetically predisposed individual |
title_full_unstemmed | Recurrent pneumothorax related to diffuse dendriform pulmonary ossification in genetically predisposed individual |
title_short | Recurrent pneumothorax related to diffuse dendriform pulmonary ossification in genetically predisposed individual |
title_sort | recurrent pneumothorax related to diffuse dendriform pulmonary ossification in genetically predisposed individual |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155673/ https://www.ncbi.nlm.nih.gov/pubmed/27999676 http://dx.doi.org/10.1002/rcr2.211 |
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