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Adalimumab induced pulmonary sarcoid reaction
Sarcoidosis is a multisystem granulomatous inflammatory disease of unknown etiology. There is evidence that Tumor Necrosis Factor alpha (TNF-α) antagonists are useful in the treatment of advanced or refractory disease. However, sarcoidosis-like reaction has been reported with TNF-α blockade in other...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920421/ https://www.ncbi.nlm.nih.gov/pubmed/26029514 http://dx.doi.org/10.1016/j.rmcr.2013.07.002 |
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author | Bhargava, S. Perlman, D.M. Allen, T.L. Ritter, J.H. Bhargava, M. |
author_facet | Bhargava, S. Perlman, D.M. Allen, T.L. Ritter, J.H. Bhargava, M. |
author_sort | Bhargava, S. |
collection | PubMed |
description | Sarcoidosis is a multisystem granulomatous inflammatory disease of unknown etiology. There is evidence that Tumor Necrosis Factor alpha (TNF-α) antagonists are useful in the treatment of advanced or refractory disease. However, sarcoidosis-like reaction has been reported with TNF-α blockade in other inflammatory conditions. Here we report a case of sarcoid-like reaction in a patient with psoriatic arthritis shortly after initiation of adalimumab therapy. Stopping adalimumab and systemic anti-inflammatory therapy with corticosteroids resulted in resolution of pulmonary symptoms and chest radiographic findings. Though TNF-α plays a critical role in pathogenesis of sarcoidosis, the development of sarcoid reaction with TNF-α blockade is paradoxical and the mechanism of this response remains unknown. TNF-α induced sarcoid-reaction could involve multiple organs. Its development with one agent does not preclude therapy with other TNF-α blockers. |
format | Online Article Text |
id | pubmed-3920421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-39204212014-10-15 Adalimumab induced pulmonary sarcoid reaction Bhargava, S. Perlman, D.M. Allen, T.L. Ritter, J.H. Bhargava, M. Respir Med Case Rep Case Report Sarcoidosis is a multisystem granulomatous inflammatory disease of unknown etiology. There is evidence that Tumor Necrosis Factor alpha (TNF-α) antagonists are useful in the treatment of advanced or refractory disease. However, sarcoidosis-like reaction has been reported with TNF-α blockade in other inflammatory conditions. Here we report a case of sarcoid-like reaction in a patient with psoriatic arthritis shortly after initiation of adalimumab therapy. Stopping adalimumab and systemic anti-inflammatory therapy with corticosteroids resulted in resolution of pulmonary symptoms and chest radiographic findings. Though TNF-α plays a critical role in pathogenesis of sarcoidosis, the development of sarcoid reaction with TNF-α blockade is paradoxical and the mechanism of this response remains unknown. TNF-α induced sarcoid-reaction could involve multiple organs. Its development with one agent does not preclude therapy with other TNF-α blockers. Elsevier 2013-10-26 /pmc/articles/PMC3920421/ /pubmed/26029514 http://dx.doi.org/10.1016/j.rmcr.2013.07.002 Text en © 2013 The Authors 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 Bhargava, S. Perlman, D.M. Allen, T.L. Ritter, J.H. Bhargava, M. Adalimumab induced pulmonary sarcoid reaction |
title | Adalimumab induced pulmonary sarcoid reaction |
title_full | Adalimumab induced pulmonary sarcoid reaction |
title_fullStr | Adalimumab induced pulmonary sarcoid reaction |
title_full_unstemmed | Adalimumab induced pulmonary sarcoid reaction |
title_short | Adalimumab induced pulmonary sarcoid reaction |
title_sort | adalimumab induced pulmonary sarcoid reaction |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920421/ https://www.ncbi.nlm.nih.gov/pubmed/26029514 http://dx.doi.org/10.1016/j.rmcr.2013.07.002 |
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