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Sarcoidosis Presenting as Acute Respiratory Distress Syndrome
Sarcoidosis is a multisystem granulomatous disease of unknown origin. It typically involves the lungs and mediastinal lymph nodes in a chronic fashion. However, acute syndrome has been reported possibly in response to systemic release of proinflammatory cytokines. Acute pulmonary manifestations, esp...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323477/ https://www.ncbi.nlm.nih.gov/pubmed/30675164 http://dx.doi.org/10.1155/2018/6465180 |
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author | Lashari, Bilal Haider Raza, Ahmad Chan, Vincent Ward, William |
author_facet | Lashari, Bilal Haider Raza, Ahmad Chan, Vincent Ward, William |
author_sort | Lashari, Bilal Haider |
collection | PubMed |
description | Sarcoidosis is a multisystem granulomatous disease of unknown origin. It typically involves the lungs and mediastinal lymph nodes in a chronic fashion. However, acute syndrome has been reported possibly in response to systemic release of proinflammatory cytokines. Acute pulmonary manifestations, especially acute respiratory failure or acute respiratory distress syndrome, remain extremely uncommon in individuals without a prior diagnosis. We present the case of a 41-year-old African American female, who presented with ARDS. An extensive workup into the cause of her illness remained negative, and she subsequently succumbed to her illness. A diagnosis of sarcoidosis was made upon autopsy, after exclusion of other granulomatous illness. The case highlights the need to consider this uncommon diagnosis in patients with unexplained ARDS to guide therapy. |
format | Online Article Text |
id | pubmed-6323477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-63234772019-01-23 Sarcoidosis Presenting as Acute Respiratory Distress Syndrome Lashari, Bilal Haider Raza, Ahmad Chan, Vincent Ward, William Case Rep Med Case Report Sarcoidosis is a multisystem granulomatous disease of unknown origin. It typically involves the lungs and mediastinal lymph nodes in a chronic fashion. However, acute syndrome has been reported possibly in response to systemic release of proinflammatory cytokines. Acute pulmonary manifestations, especially acute respiratory failure or acute respiratory distress syndrome, remain extremely uncommon in individuals without a prior diagnosis. We present the case of a 41-year-old African American female, who presented with ARDS. An extensive workup into the cause of her illness remained negative, and she subsequently succumbed to her illness. A diagnosis of sarcoidosis was made upon autopsy, after exclusion of other granulomatous illness. The case highlights the need to consider this uncommon diagnosis in patients with unexplained ARDS to guide therapy. Hindawi 2018-12-23 /pmc/articles/PMC6323477/ /pubmed/30675164 http://dx.doi.org/10.1155/2018/6465180 Text en Copyright © 2018 Bilal Haider Lashari et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Lashari, Bilal Haider Raza, Ahmad Chan, Vincent Ward, William Sarcoidosis Presenting as Acute Respiratory Distress Syndrome |
title | Sarcoidosis Presenting as Acute Respiratory Distress Syndrome |
title_full | Sarcoidosis Presenting as Acute Respiratory Distress Syndrome |
title_fullStr | Sarcoidosis Presenting as Acute Respiratory Distress Syndrome |
title_full_unstemmed | Sarcoidosis Presenting as Acute Respiratory Distress Syndrome |
title_short | Sarcoidosis Presenting as Acute Respiratory Distress Syndrome |
title_sort | sarcoidosis presenting as acute respiratory distress syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323477/ https://www.ncbi.nlm.nih.gov/pubmed/30675164 http://dx.doi.org/10.1155/2018/6465180 |
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