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Drug-induced hypersensitivity syndrome caused by minodronic acid hydrate
BACKGROUND: Drug-induced hypersensitivity syndrome (DIHS)/drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is an important adverse reaction caused by a few drugs. Reactivation of human herpesvirus 6 (HHV-6) is known to be associated with its pathogenesis. DIHS occasionally mani...
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/PMC8572576/ https://www.ncbi.nlm.nih.gov/pubmed/34743720 http://dx.doi.org/10.1186/s12890-021-01709-x |
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author | Muto, Yutaka Kuse, Naoyuki Inomata, Minoru Awano, Nobuyasu Tone, Mari Takada, Kohei Fujimoto, Kazushi Bae, Yuan Kumasaka, Toshio Izumo, Takehiro |
author_facet | Muto, Yutaka Kuse, Naoyuki Inomata, Minoru Awano, Nobuyasu Tone, Mari Takada, Kohei Fujimoto, Kazushi Bae, Yuan Kumasaka, Toshio Izumo, Takehiro |
author_sort | Muto, Yutaka |
collection | PubMed |
description | BACKGROUND: Drug-induced hypersensitivity syndrome (DIHS)/drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is an important adverse reaction caused by a few drugs. Reactivation of human herpesvirus 6 (HHV-6) is known to be associated with its pathogenesis. DIHS occasionally manifests as pulmonary lesions with a variety of imaging findings. CASE PRESENTATION: An 83-year-old woman started taking minodronic acid hydrate 5 years before admission. She noticed a generalized skin rash 44 days before admission and started oral betamethasone-d-chlorpheniramine maleate combination tablets for allergic dermatitis. She developed a fever and cough in addition to the rash, and was referred to our hospital. Laboratory data showed a high level of eosinophils and liver and biliary enzymes. Computed tomography (CT) studies revealed bilateral diffuse ground-glass opacities with ill-defined centrilobular nodules from the central to peripheral regions of the lungs. Transbronchial lung cryobiopsy specimens showed that lymphocyte infiltration was observed in the alveolar walls and fibrinous exudates and floating macrophages in the alveolar lumina. Immunohistochemistry of biopsy specimens showed more CD4(+) lymphocytes than CD8(+) lymphocytes, while few Foxp3(+) lymphocytes were recognized. The serum anti-HHV-6 immunoglobulin G titer increased at 3 weeks after the first test. Based on these findings, we diagnosed her with DIHS. We continued care without using corticosteroids since there was no worsening of breathing or skin condition. Eventually, her clinical symptoms chest CT had improved. Minodronic acid hydrate was identified as the culprit drug based on the positive results of the patch test and drug-induced lymphocyte stimulation test. CONCLUSIONS: We described the first case of DIHS caused by minodronic acid hydrate. Lung lesions in DIHS can present with bilateral diffuse ground-glass opacities and ill-defined centrilobular nodules on a CT scan during the recovery phase. Clinicians should be aware of DIHS, even if patients are not involved with typical DIHS/DRESS-causing drugs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12890-021-01709-x. |
format | Online Article Text |
id | pubmed-8572576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85725762021-11-08 Drug-induced hypersensitivity syndrome caused by minodronic acid hydrate Muto, Yutaka Kuse, Naoyuki Inomata, Minoru Awano, Nobuyasu Tone, Mari Takada, Kohei Fujimoto, Kazushi Bae, Yuan Kumasaka, Toshio Izumo, Takehiro BMC Pulm Med Case Report BACKGROUND: Drug-induced hypersensitivity syndrome (DIHS)/drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is an important adverse reaction caused by a few drugs. Reactivation of human herpesvirus 6 (HHV-6) is known to be associated with its pathogenesis. DIHS occasionally manifests as pulmonary lesions with a variety of imaging findings. CASE PRESENTATION: An 83-year-old woman started taking minodronic acid hydrate 5 years before admission. She noticed a generalized skin rash 44 days before admission and started oral betamethasone-d-chlorpheniramine maleate combination tablets for allergic dermatitis. She developed a fever and cough in addition to the rash, and was referred to our hospital. Laboratory data showed a high level of eosinophils and liver and biliary enzymes. Computed tomography (CT) studies revealed bilateral diffuse ground-glass opacities with ill-defined centrilobular nodules from the central to peripheral regions of the lungs. Transbronchial lung cryobiopsy specimens showed that lymphocyte infiltration was observed in the alveolar walls and fibrinous exudates and floating macrophages in the alveolar lumina. Immunohistochemistry of biopsy specimens showed more CD4(+) lymphocytes than CD8(+) lymphocytes, while few Foxp3(+) lymphocytes were recognized. The serum anti-HHV-6 immunoglobulin G titer increased at 3 weeks after the first test. Based on these findings, we diagnosed her with DIHS. We continued care without using corticosteroids since there was no worsening of breathing or skin condition. Eventually, her clinical symptoms chest CT had improved. Minodronic acid hydrate was identified as the culprit drug based on the positive results of the patch test and drug-induced lymphocyte stimulation test. CONCLUSIONS: We described the first case of DIHS caused by minodronic acid hydrate. Lung lesions in DIHS can present with bilateral diffuse ground-glass opacities and ill-defined centrilobular nodules on a CT scan during the recovery phase. Clinicians should be aware of DIHS, even if patients are not involved with typical DIHS/DRESS-causing drugs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12890-021-01709-x. BioMed Central 2021-11-07 /pmc/articles/PMC8572576/ /pubmed/34743720 http://dx.doi.org/10.1186/s12890-021-01709-x 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 Muto, Yutaka Kuse, Naoyuki Inomata, Minoru Awano, Nobuyasu Tone, Mari Takada, Kohei Fujimoto, Kazushi Bae, Yuan Kumasaka, Toshio Izumo, Takehiro Drug-induced hypersensitivity syndrome caused by minodronic acid hydrate |
title | Drug-induced hypersensitivity syndrome caused by minodronic acid hydrate |
title_full | Drug-induced hypersensitivity syndrome caused by minodronic acid hydrate |
title_fullStr | Drug-induced hypersensitivity syndrome caused by minodronic acid hydrate |
title_full_unstemmed | Drug-induced hypersensitivity syndrome caused by minodronic acid hydrate |
title_short | Drug-induced hypersensitivity syndrome caused by minodronic acid hydrate |
title_sort | drug-induced hypersensitivity syndrome caused by minodronic acid hydrate |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572576/ https://www.ncbi.nlm.nih.gov/pubmed/34743720 http://dx.doi.org/10.1186/s12890-021-01709-x |
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