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Clinically Amyopathic Dermatomyositis with Interstitial Pneumonia That Was Successfully Treated with Plasma Exchange
Patients with clinically amyopathic dermatomyositis (CADM), a subset of dermatomyositis characterized by a lack of muscle involvement, frequently develop rapidly progressive and treatment-resistant interstitial lung disease. We report the case of a 49-year-old man who was diagnosed with CADM. He dev...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Internal Medicine
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6064687/ https://www.ncbi.nlm.nih.gov/pubmed/29491297 http://dx.doi.org/10.2169/internalmedicine.0297-17 |
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author | Yagishita, Mizuki Kondo, Yuya Terasaki, Toshihiko Terasaki, Mayu Shimizu, Masaru Honda, Fumika Oyama, Ayako Takahashi, Hiroyuki Yokosawa, Masahiro Asashima, Hiromitsu Hagiwara, Shinya Tsuboi, Hiroto Matsumoto, Isao Sumida, Takayuki |
author_facet | Yagishita, Mizuki Kondo, Yuya Terasaki, Toshihiko Terasaki, Mayu Shimizu, Masaru Honda, Fumika Oyama, Ayako Takahashi, Hiroyuki Yokosawa, Masahiro Asashima, Hiromitsu Hagiwara, Shinya Tsuboi, Hiroto Matsumoto, Isao Sumida, Takayuki |
author_sort | Yagishita, Mizuki |
collection | PubMed |
description | Patients with clinically amyopathic dermatomyositis (CADM), a subset of dermatomyositis characterized by a lack of muscle involvement, frequently develop rapidly progressive and treatment-resistant interstitial lung disease. We report the case of a 49-year-old man who was diagnosed with CADM. He developed interstitial pneumonia, which did not respond to combination therapy with methylprednisolone pulse therapy, cyclophosphamide, and cyclosporine. We therefore attempted plasma exchange. After 7 courses of therapeutic plasma exchange, the interstitial pneumonia gradually improved. This case suggests that plasma exchange might be an effective therapeutic option for patients with progressive interstitial lung disease in steroid- and immunosuppressive therapy-refractive CADM. |
format | Online Article Text |
id | pubmed-6064687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Japanese Society of Internal Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-60646872018-07-30 Clinically Amyopathic Dermatomyositis with Interstitial Pneumonia That Was Successfully Treated with Plasma Exchange Yagishita, Mizuki Kondo, Yuya Terasaki, Toshihiko Terasaki, Mayu Shimizu, Masaru Honda, Fumika Oyama, Ayako Takahashi, Hiroyuki Yokosawa, Masahiro Asashima, Hiromitsu Hagiwara, Shinya Tsuboi, Hiroto Matsumoto, Isao Sumida, Takayuki Intern Med Case Report Patients with clinically amyopathic dermatomyositis (CADM), a subset of dermatomyositis characterized by a lack of muscle involvement, frequently develop rapidly progressive and treatment-resistant interstitial lung disease. We report the case of a 49-year-old man who was diagnosed with CADM. He developed interstitial pneumonia, which did not respond to combination therapy with methylprednisolone pulse therapy, cyclophosphamide, and cyclosporine. We therefore attempted plasma exchange. After 7 courses of therapeutic plasma exchange, the interstitial pneumonia gradually improved. This case suggests that plasma exchange might be an effective therapeutic option for patients with progressive interstitial lung disease in steroid- and immunosuppressive therapy-refractive CADM. The Japanese Society of Internal Medicine 2018-02-28 2018-07-01 /pmc/articles/PMC6064687/ /pubmed/29491297 http://dx.doi.org/10.2169/internalmedicine.0297-17 Text en Copyright © 2018 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access article 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 Yagishita, Mizuki Kondo, Yuya Terasaki, Toshihiko Terasaki, Mayu Shimizu, Masaru Honda, Fumika Oyama, Ayako Takahashi, Hiroyuki Yokosawa, Masahiro Asashima, Hiromitsu Hagiwara, Shinya Tsuboi, Hiroto Matsumoto, Isao Sumida, Takayuki Clinically Amyopathic Dermatomyositis with Interstitial Pneumonia That Was Successfully Treated with Plasma Exchange |
title | Clinically Amyopathic Dermatomyositis with Interstitial Pneumonia That Was Successfully Treated with Plasma Exchange |
title_full | Clinically Amyopathic Dermatomyositis with Interstitial Pneumonia That Was Successfully Treated with Plasma Exchange |
title_fullStr | Clinically Amyopathic Dermatomyositis with Interstitial Pneumonia That Was Successfully Treated with Plasma Exchange |
title_full_unstemmed | Clinically Amyopathic Dermatomyositis with Interstitial Pneumonia That Was Successfully Treated with Plasma Exchange |
title_short | Clinically Amyopathic Dermatomyositis with Interstitial Pneumonia That Was Successfully Treated with Plasma Exchange |
title_sort | clinically amyopathic dermatomyositis with interstitial pneumonia that was successfully treated with plasma exchange |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6064687/ https://www.ncbi.nlm.nih.gov/pubmed/29491297 http://dx.doi.org/10.2169/internalmedicine.0297-17 |
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