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Sarcoidosis presenting with glazy mucoid sputum and dyspnea: a case report
BACKGROUND: Patients with pulmonary sarcoidosis commonly present with a dry cough; a productive cough suggests a complicating airway infection or an alternative diagnosis such as tuberculosis or bronchiectasis. CASE PRESENTATION: A 36-year-old European (Frisian) woman recently diagnosed with pulmona...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110313/ https://www.ncbi.nlm.nih.gov/pubmed/33971963 http://dx.doi.org/10.1186/s13256-021-02809-2 |
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author | Al-Kailany, Wud Timens, Wim Venmans, Ben de Jonge, Gonda van der Werf, Tjip S. |
author_facet | Al-Kailany, Wud Timens, Wim Venmans, Ben de Jonge, Gonda van der Werf, Tjip S. |
author_sort | Al-Kailany, Wud |
collection | PubMed |
description | BACKGROUND: Patients with pulmonary sarcoidosis commonly present with a dry cough; a productive cough suggests a complicating airway infection or an alternative diagnosis such as tuberculosis or bronchiectasis. CASE PRESENTATION: A 36-year-old European (Frisian) woman recently diagnosed with pulmonary sarcoidosis presented with debilitating exertional dyspnea and cough productive of glazy mucoid sputum. Several different attempts including video-assisted thoracoscopic biopsies failed to reach a second or alternative diagnosis including an infectious, autoimmune or collagen-vascular condition. She responded to steroids but with poor tolerance to this treatment, which could not be tapered. After she was started on anti-tumor necrosis factor alpha (TNF-α) therapy with infliximab, 200 mg at three-monthly intervals, she has been fine for well over a decade. CONCLUSIONS: In this patient with sarcoidosis who had a productive cough accompanied by fever, an extensive workup and prolonged follow-up, an alternative or second diagnosis could be ruled out; we therefore conclude that this highly unusual presentation is part of the clinical spectrum of sarcoidosis. |
format | Online Article Text |
id | pubmed-8110313 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81103132021-05-11 Sarcoidosis presenting with glazy mucoid sputum and dyspnea: a case report Al-Kailany, Wud Timens, Wim Venmans, Ben de Jonge, Gonda van der Werf, Tjip S. J Med Case Rep Case Report BACKGROUND: Patients with pulmonary sarcoidosis commonly present with a dry cough; a productive cough suggests a complicating airway infection or an alternative diagnosis such as tuberculosis or bronchiectasis. CASE PRESENTATION: A 36-year-old European (Frisian) woman recently diagnosed with pulmonary sarcoidosis presented with debilitating exertional dyspnea and cough productive of glazy mucoid sputum. Several different attempts including video-assisted thoracoscopic biopsies failed to reach a second or alternative diagnosis including an infectious, autoimmune or collagen-vascular condition. She responded to steroids but with poor tolerance to this treatment, which could not be tapered. After she was started on anti-tumor necrosis factor alpha (TNF-α) therapy with infliximab, 200 mg at three-monthly intervals, she has been fine for well over a decade. CONCLUSIONS: In this patient with sarcoidosis who had a productive cough accompanied by fever, an extensive workup and prolonged follow-up, an alternative or second diagnosis could be ruled out; we therefore conclude that this highly unusual presentation is part of the clinical spectrum of sarcoidosis. BioMed Central 2021-05-11 /pmc/articles/PMC8110313/ /pubmed/33971963 http://dx.doi.org/10.1186/s13256-021-02809-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Al-Kailany, Wud Timens, Wim Venmans, Ben de Jonge, Gonda van der Werf, Tjip S. Sarcoidosis presenting with glazy mucoid sputum and dyspnea: a case report |
title | Sarcoidosis presenting with glazy mucoid sputum and dyspnea: a case report |
title_full | Sarcoidosis presenting with glazy mucoid sputum and dyspnea: a case report |
title_fullStr | Sarcoidosis presenting with glazy mucoid sputum and dyspnea: a case report |
title_full_unstemmed | Sarcoidosis presenting with glazy mucoid sputum and dyspnea: a case report |
title_short | Sarcoidosis presenting with glazy mucoid sputum and dyspnea: a case report |
title_sort | sarcoidosis presenting with glazy mucoid sputum and dyspnea: a case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8110313/ https://www.ncbi.nlm.nih.gov/pubmed/33971963 http://dx.doi.org/10.1186/s13256-021-02809-2 |
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