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Anti‐TIF1γ antibody‐positive dermatomyositis associated with durvalumab administration in a patient with lung and oesophageal cancers
We report a case of anti‐transcriptional intermediary factor 1γ (TIF1γ) antibody‐positive dermatomyositis following durvalumab treatment. The patient was successfully treated with pulse steroid therapy, high‐dose intravenous immunoglobulin (IVIg), and tacrolimus. Durvalumab may induce dermatomyositi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985661/ https://www.ncbi.nlm.nih.gov/pubmed/33777398 http://dx.doi.org/10.1002/rcr2.736 |
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author | Imai, Ryosuke Ikemura, Sumie Jinta, Torahiko |
author_facet | Imai, Ryosuke Ikemura, Sumie Jinta, Torahiko |
author_sort | Imai, Ryosuke |
collection | PubMed |
description | We report a case of anti‐transcriptional intermediary factor 1γ (TIF1γ) antibody‐positive dermatomyositis following durvalumab treatment. The patient was successfully treated with pulse steroid therapy, high‐dose intravenous immunoglobulin (IVIg), and tacrolimus. Durvalumab may induce dermatomyositis, and early diagnosis and aggressive therapy are crucial to prevent severe dermatomyositis, which is potentially treatable. |
format | Online Article Text |
id | pubmed-7985661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-79856612021-03-25 Anti‐TIF1γ antibody‐positive dermatomyositis associated with durvalumab administration in a patient with lung and oesophageal cancers Imai, Ryosuke Ikemura, Sumie Jinta, Torahiko Respirol Case Rep Case Reports We report a case of anti‐transcriptional intermediary factor 1γ (TIF1γ) antibody‐positive dermatomyositis following durvalumab treatment. The patient was successfully treated with pulse steroid therapy, high‐dose intravenous immunoglobulin (IVIg), and tacrolimus. Durvalumab may induce dermatomyositis, and early diagnosis and aggressive therapy are crucial to prevent severe dermatomyositis, which is potentially treatable. John Wiley & Sons, Ltd 2021-03-23 /pmc/articles/PMC7985661/ /pubmed/33777398 http://dx.doi.org/10.1002/rcr2.736 Text en © 2021 The Authors. Respirology Case Reports published by John Wiley & Sons Australia, Ltd on behalf of The Asian Pacific Society of Respirology. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Imai, Ryosuke Ikemura, Sumie Jinta, Torahiko Anti‐TIF1γ antibody‐positive dermatomyositis associated with durvalumab administration in a patient with lung and oesophageal cancers |
title |
Anti‐TIF1γ antibody‐positive dermatomyositis associated with durvalumab administration in a patient with lung and oesophageal cancers |
title_full |
Anti‐TIF1γ antibody‐positive dermatomyositis associated with durvalumab administration in a patient with lung and oesophageal cancers |
title_fullStr |
Anti‐TIF1γ antibody‐positive dermatomyositis associated with durvalumab administration in a patient with lung and oesophageal cancers |
title_full_unstemmed |
Anti‐TIF1γ antibody‐positive dermatomyositis associated with durvalumab administration in a patient with lung and oesophageal cancers |
title_short |
Anti‐TIF1γ antibody‐positive dermatomyositis associated with durvalumab administration in a patient with lung and oesophageal cancers |
title_sort | anti‐tif1γ antibody‐positive dermatomyositis associated with durvalumab administration in a patient with lung and oesophageal cancers |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985661/ https://www.ncbi.nlm.nih.gov/pubmed/33777398 http://dx.doi.org/10.1002/rcr2.736 |
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