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Sclerosing Mediastinitis Causing Unilateral Pulmonary Edema Due to Left Atrial and Pulmonary Venous Compression. A Case Report and Literature Review
Sclerosing mediastinitis (SM), previously named chronic fibrosing mediastinitis, is an inflammatory process that in its end-stage results to sclerosis around the mediastinal structures. SM is quite rare and has been correlated with inflammatory and autoimmune diseases, as well as malignancy. SM may...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Cirurgia Cardiovascular
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385839/ https://www.ncbi.nlm.nih.gov/pubmed/30810679 http://dx.doi.org/10.21470/1678-9741-2018-0067 |
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author | Panagopoulos, Nikolaos Leivaditis, Vasileios Kraniotis, Pantelis Ravazoula, Panagiota Koletsis, Efstratios Dougenis, Dimitrios |
author_facet | Panagopoulos, Nikolaos Leivaditis, Vasileios Kraniotis, Pantelis Ravazoula, Panagiota Koletsis, Efstratios Dougenis, Dimitrios |
author_sort | Panagopoulos, Nikolaos |
collection | PubMed |
description | Sclerosing mediastinitis (SM), previously named chronic fibrosing mediastinitis, is an inflammatory process that in its end-stage results to sclerosis around the mediastinal structures. SM is quite rare and has been correlated with inflammatory and autoimmune diseases, as well as malignancy. SM may either present in a mild form, with minor symptoms and a benign course or in a more aggressive form with severe pulmonary hypertension and subsequent higher morbidity and mortality. The diagnosis of SM may be difficult and quite challenging, as symptoms depend on the mediastinal structure that is mainly involved; quite often the superior vena cava. However, practically any mediastinal structure may be involved by the fibrotic process, such as the central airways, as well as the pulmonary arteries and veins, leading to obstruction or total occlusion. The latter may be impossible to undergo proper surgical excision of the lesion, and is considered to be a real challenge to the surgeon. We herein report a case of SM that presented with arterial and venous compression. The imaging appearance was that of unilateral pulmonary edema, associated with lung collapse. The case is supplemented by a non-systematic review of the relevant literature. |
format | Online Article Text |
id | pubmed-6385839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Sociedade Brasileira de Cirurgia Cardiovascular |
record_format | MEDLINE/PubMed |
spelling | pubmed-63858392019-02-27 Sclerosing Mediastinitis Causing Unilateral Pulmonary Edema Due to Left Atrial and Pulmonary Venous Compression. A Case Report and Literature Review Panagopoulos, Nikolaos Leivaditis, Vasileios Kraniotis, Pantelis Ravazoula, Panagiota Koletsis, Efstratios Dougenis, Dimitrios Braz J Cardiovasc Surg Review Article Sclerosing mediastinitis (SM), previously named chronic fibrosing mediastinitis, is an inflammatory process that in its end-stage results to sclerosis around the mediastinal structures. SM is quite rare and has been correlated with inflammatory and autoimmune diseases, as well as malignancy. SM may either present in a mild form, with minor symptoms and a benign course or in a more aggressive form with severe pulmonary hypertension and subsequent higher morbidity and mortality. The diagnosis of SM may be difficult and quite challenging, as symptoms depend on the mediastinal structure that is mainly involved; quite often the superior vena cava. However, practically any mediastinal structure may be involved by the fibrotic process, such as the central airways, as well as the pulmonary arteries and veins, leading to obstruction or total occlusion. The latter may be impossible to undergo proper surgical excision of the lesion, and is considered to be a real challenge to the surgeon. We herein report a case of SM that presented with arterial and venous compression. The imaging appearance was that of unilateral pulmonary edema, associated with lung collapse. The case is supplemented by a non-systematic review of the relevant literature. Sociedade Brasileira de Cirurgia Cardiovascular 2019 /pmc/articles/PMC6385839/ /pubmed/30810679 http://dx.doi.org/10.21470/1678-9741-2018-0067 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Panagopoulos, Nikolaos Leivaditis, Vasileios Kraniotis, Pantelis Ravazoula, Panagiota Koletsis, Efstratios Dougenis, Dimitrios Sclerosing Mediastinitis Causing Unilateral Pulmonary Edema Due to Left Atrial and Pulmonary Venous Compression. A Case Report and Literature Review |
title | Sclerosing Mediastinitis Causing Unilateral Pulmonary Edema Due to
Left Atrial and Pulmonary Venous Compression. A Case Report and Literature
Review |
title_full | Sclerosing Mediastinitis Causing Unilateral Pulmonary Edema Due to
Left Atrial and Pulmonary Venous Compression. A Case Report and Literature
Review |
title_fullStr | Sclerosing Mediastinitis Causing Unilateral Pulmonary Edema Due to
Left Atrial and Pulmonary Venous Compression. A Case Report and Literature
Review |
title_full_unstemmed | Sclerosing Mediastinitis Causing Unilateral Pulmonary Edema Due to
Left Atrial and Pulmonary Venous Compression. A Case Report and Literature
Review |
title_short | Sclerosing Mediastinitis Causing Unilateral Pulmonary Edema Due to
Left Atrial and Pulmonary Venous Compression. A Case Report and Literature
Review |
title_sort | sclerosing mediastinitis causing unilateral pulmonary edema due to
left atrial and pulmonary venous compression. a case report and literature
review |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6385839/ https://www.ncbi.nlm.nih.gov/pubmed/30810679 http://dx.doi.org/10.21470/1678-9741-2018-0067 |
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