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Acute respiratory distress syndrome in a patient with primary myelofibrosis after ruxolitinib treatment discontinuation
Ruxolitinib is a Janus kinase (JAK) inhibitor used for the treatment of myelofibrosis with demonstrated efficacy for the alleviation of disease-related symptoms and splenomegaly. Anemia and thrombocytopenia are the main secondary effects. However, there are case reports of rare but serious adverse e...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Japan
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7100122/ https://www.ncbi.nlm.nih.gov/pubmed/25034748 http://dx.doi.org/10.1007/s12185-014-1628-5 |
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author | Beauverd, Yan Samii, Kaveh |
author_facet | Beauverd, Yan Samii, Kaveh |
author_sort | Beauverd, Yan |
collection | PubMed |
description | Ruxolitinib is a Janus kinase (JAK) inhibitor used for the treatment of myelofibrosis with demonstrated efficacy for the alleviation of disease-related symptoms and splenomegaly. Anemia and thrombocytopenia are the main secondary effects. However, there are case reports of rare but serious adverse events following drug withdrawal. We present a case of a 76-year-old man diagnosed with primary myelofibrosis who presented with constitutional symptoms and symptomatic splenomegaly. Ruxolitinib was started (15 mg twice daily) and his disease-related symptoms disappeared. Six weeks later, he developed grade 4 thrombocytopenia and grade 3 anemia. Ruxolitinib was stopped and corticosteroid treatment (prednisone 1 mg/kg/day) was started to avoid a cytokine-rebound reaction. The patient then developed fever, chills, a biological inflammatory syndrome, and an acute respiratory disease syndrome. Full workup excluded an infection and we concluded that ruxolitinib withdrawal syndrome was the likely cause. Continued treatment with corticosteroids, as well as oxygen supply and continuous positive airway pressure, allowed an alleviation of his symptoms. This case report describes acute respiratory distress syndrome as another potential complication of ruxolitinib withdrawal syndrome. |
format | Online Article Text |
id | pubmed-7100122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-71001222020-03-27 Acute respiratory distress syndrome in a patient with primary myelofibrosis after ruxolitinib treatment discontinuation Beauverd, Yan Samii, Kaveh Int J Hematol Case Report Ruxolitinib is a Janus kinase (JAK) inhibitor used for the treatment of myelofibrosis with demonstrated efficacy for the alleviation of disease-related symptoms and splenomegaly. Anemia and thrombocytopenia are the main secondary effects. However, there are case reports of rare but serious adverse events following drug withdrawal. We present a case of a 76-year-old man diagnosed with primary myelofibrosis who presented with constitutional symptoms and symptomatic splenomegaly. Ruxolitinib was started (15 mg twice daily) and his disease-related symptoms disappeared. Six weeks later, he developed grade 4 thrombocytopenia and grade 3 anemia. Ruxolitinib was stopped and corticosteroid treatment (prednisone 1 mg/kg/day) was started to avoid a cytokine-rebound reaction. The patient then developed fever, chills, a biological inflammatory syndrome, and an acute respiratory disease syndrome. Full workup excluded an infection and we concluded that ruxolitinib withdrawal syndrome was the likely cause. Continued treatment with corticosteroids, as well as oxygen supply and continuous positive airway pressure, allowed an alleviation of his symptoms. This case report describes acute respiratory distress syndrome as another potential complication of ruxolitinib withdrawal syndrome. Springer Japan 2014-07-18 2014 /pmc/articles/PMC7100122/ /pubmed/25034748 http://dx.doi.org/10.1007/s12185-014-1628-5 Text en © The Japanese Society of Hematology 2014 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Case Report Beauverd, Yan Samii, Kaveh Acute respiratory distress syndrome in a patient with primary myelofibrosis after ruxolitinib treatment discontinuation |
title | Acute respiratory distress syndrome in a patient with primary myelofibrosis after ruxolitinib treatment discontinuation |
title_full | Acute respiratory distress syndrome in a patient with primary myelofibrosis after ruxolitinib treatment discontinuation |
title_fullStr | Acute respiratory distress syndrome in a patient with primary myelofibrosis after ruxolitinib treatment discontinuation |
title_full_unstemmed | Acute respiratory distress syndrome in a patient with primary myelofibrosis after ruxolitinib treatment discontinuation |
title_short | Acute respiratory distress syndrome in a patient with primary myelofibrosis after ruxolitinib treatment discontinuation |
title_sort | acute respiratory distress syndrome in a patient with primary myelofibrosis after ruxolitinib treatment discontinuation |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7100122/ https://www.ncbi.nlm.nih.gov/pubmed/25034748 http://dx.doi.org/10.1007/s12185-014-1628-5 |
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