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Sarcoid-like Granulomatous Lung Disease with Subacute Progression in Silicosis
A 67-year-old man was admitted to our hospital with cough and fatigue. He had had long-term exposure to silica due to cement processing. Chest computed tomography showed bilateral centrilobular nodules, and hilar and mediastinal lymphadenopathy with calcification, suggesting chronic silicosis. Withi...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Internal Medicine
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866780/ https://www.ncbi.nlm.nih.gov/pubmed/34334564 http://dx.doi.org/10.2169/internalmedicine.7533-21 |
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author | Mochizuka, Yasutaka Kono, Masato Katsumata, Mineo Hirama, Ryutaro Watanuki, Masayuki Oshima, Yuiko Takeda, Kenichiro Tsutsumi, Akari Miwa, Hideki Miki, Yoshihiro Hashimoto, Dai Enomoto, Noriyuki Nakamura, Yutaro Suda, Takafumi Nakamura, Hidenori |
author_facet | Mochizuka, Yasutaka Kono, Masato Katsumata, Mineo Hirama, Ryutaro Watanuki, Masayuki Oshima, Yuiko Takeda, Kenichiro Tsutsumi, Akari Miwa, Hideki Miki, Yoshihiro Hashimoto, Dai Enomoto, Noriyuki Nakamura, Yutaro Suda, Takafumi Nakamura, Hidenori |
author_sort | Mochizuka, Yasutaka |
collection | PubMed |
description | A 67-year-old man was admitted to our hospital with cough and fatigue. He had had long-term exposure to silica due to cement processing. Chest computed tomography showed bilateral centrilobular nodules, and hilar and mediastinal lymphadenopathy with calcification, suggesting chronic silicosis. Within a few months, these nodules enlarged, and bilateral patchy consolidations appeared. A lung biopsy revealed sarcoid-like granulomas with birefringent particles under polarized light without malignancy or infection. He was diagnosed with silicosis-associated sarcoid-like granulomatous lung disease, rather than sarcoidosis, according to the clinicopathological findings. His pulmonary manifestations improved after the discontinuation of silica exposure and combination therapy of corticosteroid and azathioprine. |
format | Online Article Text |
id | pubmed-8866780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Japanese Society of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-88667802022-03-14 Sarcoid-like Granulomatous Lung Disease with Subacute Progression in Silicosis Mochizuka, Yasutaka Kono, Masato Katsumata, Mineo Hirama, Ryutaro Watanuki, Masayuki Oshima, Yuiko Takeda, Kenichiro Tsutsumi, Akari Miwa, Hideki Miki, Yoshihiro Hashimoto, Dai Enomoto, Noriyuki Nakamura, Yutaro Suda, Takafumi Nakamura, Hidenori Intern Med Case Report A 67-year-old man was admitted to our hospital with cough and fatigue. He had had long-term exposure to silica due to cement processing. Chest computed tomography showed bilateral centrilobular nodules, and hilar and mediastinal lymphadenopathy with calcification, suggesting chronic silicosis. Within a few months, these nodules enlarged, and bilateral patchy consolidations appeared. A lung biopsy revealed sarcoid-like granulomas with birefringent particles under polarized light without malignancy or infection. He was diagnosed with silicosis-associated sarcoid-like granulomatous lung disease, rather than sarcoidosis, according to the clinicopathological findings. His pulmonary manifestations improved after the discontinuation of silica exposure and combination therapy of corticosteroid and azathioprine. The Japanese Society of Internal Medicine 2021-07-30 2022-02-01 /pmc/articles/PMC8866780/ /pubmed/34334564 http://dx.doi.org/10.2169/internalmedicine.7533-21 Text en Copyright © 2022 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/The Internal Medicine is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Mochizuka, Yasutaka Kono, Masato Katsumata, Mineo Hirama, Ryutaro Watanuki, Masayuki Oshima, Yuiko Takeda, Kenichiro Tsutsumi, Akari Miwa, Hideki Miki, Yoshihiro Hashimoto, Dai Enomoto, Noriyuki Nakamura, Yutaro Suda, Takafumi Nakamura, Hidenori Sarcoid-like Granulomatous Lung Disease with Subacute Progression in Silicosis |
title | Sarcoid-like Granulomatous Lung Disease with Subacute Progression in Silicosis |
title_full | Sarcoid-like Granulomatous Lung Disease with Subacute Progression in Silicosis |
title_fullStr | Sarcoid-like Granulomatous Lung Disease with Subacute Progression in Silicosis |
title_full_unstemmed | Sarcoid-like Granulomatous Lung Disease with Subacute Progression in Silicosis |
title_short | Sarcoid-like Granulomatous Lung Disease with Subacute Progression in Silicosis |
title_sort | sarcoid-like granulomatous lung disease with subacute progression in silicosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8866780/ https://www.ncbi.nlm.nih.gov/pubmed/34334564 http://dx.doi.org/10.2169/internalmedicine.7533-21 |
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