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Spontaneous improvement of laryngeal sarcoidosis resistant to systemic corticosteroid administration
We report herein a case of laryngeal sarcoidosis that was refractory to systemic corticosteroids, but that improved spontaneously. A 49-year-old woman complained of dysphagia and hoarseness with accompanying edematous swellings of both arytenoid regions. She was referred to our hospital after system...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571742/ https://www.ncbi.nlm.nih.gov/pubmed/26392860 http://dx.doi.org/10.1002/rcr2.118 |
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author | Tsubouchi, Kazuya Hamada, Naoki Ijichi, Kayo Umezaki, Toshiro Takayama, Koichi Nakanishi, Yoichi |
author_facet | Tsubouchi, Kazuya Hamada, Naoki Ijichi, Kayo Umezaki, Toshiro Takayama, Koichi Nakanishi, Yoichi |
author_sort | Tsubouchi, Kazuya |
collection | PubMed |
description | We report herein a case of laryngeal sarcoidosis that was refractory to systemic corticosteroids, but that improved spontaneously. A 49-year-old woman complained of dysphagia and hoarseness with accompanying edematous swellings of both arytenoid regions. She was referred to our hospital after systemic corticosteroid therapy failed to achieve any improvement. Laryngoscopy showed marked edema of the epiglottis and both arytenoid regions. The flow–volume curve on spirometry showed flattening of the expiratory flows. Histopathological examination of the arytenoid region showed non-caseating epithelioid granulomas, and laryngeal sarcoidosis was diagnosed with the result of BAL study. She was observed without treatment as symptoms were mild. Although edema of the left arytenoid region seemed to be somewhat worsened after 6 months, she continued to be followed closely because of improvements in the flow–volume curve and increasing peak expiratory flow. By 1 year after onset, symptoms and epiglottal swelling had spontaneously improved. |
format | Online Article Text |
id | pubmed-4571742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-45717422015-09-21 Spontaneous improvement of laryngeal sarcoidosis resistant to systemic corticosteroid administration Tsubouchi, Kazuya Hamada, Naoki Ijichi, Kayo Umezaki, Toshiro Takayama, Koichi Nakanishi, Yoichi Respirol Case Rep Case Reports We report herein a case of laryngeal sarcoidosis that was refractory to systemic corticosteroids, but that improved spontaneously. A 49-year-old woman complained of dysphagia and hoarseness with accompanying edematous swellings of both arytenoid regions. She was referred to our hospital after systemic corticosteroid therapy failed to achieve any improvement. Laryngoscopy showed marked edema of the epiglottis and both arytenoid regions. The flow–volume curve on spirometry showed flattening of the expiratory flows. Histopathological examination of the arytenoid region showed non-caseating epithelioid granulomas, and laryngeal sarcoidosis was diagnosed with the result of BAL study. She was observed without treatment as symptoms were mild. Although edema of the left arytenoid region seemed to be somewhat worsened after 6 months, she continued to be followed closely because of improvements in the flow–volume curve and increasing peak expiratory flow. By 1 year after onset, symptoms and epiglottal swelling had spontaneously improved. John Wiley & Sons, Ltd 2015-09 2015-08-13 /pmc/articles/PMC4571742/ /pubmed/26392860 http://dx.doi.org/10.1002/rcr2.118 Text en © 2015 The Authors. Respirology Case Reports published by John Wiley & Sons Ltd on behalf of The Asian Pacific Society of Respirology. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial 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 Tsubouchi, Kazuya Hamada, Naoki Ijichi, Kayo Umezaki, Toshiro Takayama, Koichi Nakanishi, Yoichi Spontaneous improvement of laryngeal sarcoidosis resistant to systemic corticosteroid administration |
title | Spontaneous improvement of laryngeal sarcoidosis resistant to systemic corticosteroid administration |
title_full | Spontaneous improvement of laryngeal sarcoidosis resistant to systemic corticosteroid administration |
title_fullStr | Spontaneous improvement of laryngeal sarcoidosis resistant to systemic corticosteroid administration |
title_full_unstemmed | Spontaneous improvement of laryngeal sarcoidosis resistant to systemic corticosteroid administration |
title_short | Spontaneous improvement of laryngeal sarcoidosis resistant to systemic corticosteroid administration |
title_sort | spontaneous improvement of laryngeal sarcoidosis resistant to systemic corticosteroid administration |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4571742/ https://www.ncbi.nlm.nih.gov/pubmed/26392860 http://dx.doi.org/10.1002/rcr2.118 |
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