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Pulmonary cryptococcosis in a ruxolitinib-treated patient with primary myelofibrosis
We present the case of a 79-year-old man who showed multiple pulmonary nodules on chest computed tomography (CT) after being treated for 6 months with ruxolitinib, an inhibitor of Janus kinase (JAK) 1 and 2, to treat primary myelofibrosis. We examined the lesions by bronchoscopy, and the biopsy spec...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499110/ https://www.ncbi.nlm.nih.gov/pubmed/28721333 http://dx.doi.org/10.1016/j.rmcr.2017.06.015 |
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author | Hirano, Anna Yamasaki, Masahiro Saito, Naomi Iwato, Koji Daido, Wakako Funaishi, Kunihiko Ishiyama, Sayaka Deguchi, Naoko Taniwaki, Masaya Ohashi, Nobuyuki |
author_facet | Hirano, Anna Yamasaki, Masahiro Saito, Naomi Iwato, Koji Daido, Wakako Funaishi, Kunihiko Ishiyama, Sayaka Deguchi, Naoko Taniwaki, Masaya Ohashi, Nobuyuki |
author_sort | Hirano, Anna |
collection | PubMed |
description | We present the case of a 79-year-old man who showed multiple pulmonary nodules on chest computed tomography (CT) after being treated for 6 months with ruxolitinib, an inhibitor of Janus kinase (JAK) 1 and 2, to treat primary myelofibrosis. We examined the lesions by bronchoscopy, and the biopsy specimen revealed fungus bodies of Cryptococcus with granulomatous inflammation. As a result, the patient was diagnosed with pulmonary cryptococcosis. The patient was treated with fluconazole (200 mg daily for 2 weeks) with concomitant ruxolitinib administration, but the pulmonary lesions progressed. Subsequently, the patient was treated with voriconazole (300 mg daily for 3 weeks), but the lesions worsened further. The administration of ruxolitinib was therefore discontinued, and the dosage of voriconazole was increased to 400 mg daily. Three months later, the pulmonary lesions diminished in size. The present case of pulmonary cryptococcosis occurred in a patient treated with ruxolitinib. Treatment of pulmonary cryptococcosis with concomitant JAK inhibitor administration may result in poor treatment efficacy. It might be better to stop administration of JAK inhibitors, if possible, in patients being treated for pulmonary cryptococcosis. |
format | Online Article Text |
id | pubmed-5499110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-54991102017-07-18 Pulmonary cryptococcosis in a ruxolitinib-treated patient with primary myelofibrosis Hirano, Anna Yamasaki, Masahiro Saito, Naomi Iwato, Koji Daido, Wakako Funaishi, Kunihiko Ishiyama, Sayaka Deguchi, Naoko Taniwaki, Masaya Ohashi, Nobuyuki Respir Med Case Rep Case Report We present the case of a 79-year-old man who showed multiple pulmonary nodules on chest computed tomography (CT) after being treated for 6 months with ruxolitinib, an inhibitor of Janus kinase (JAK) 1 and 2, to treat primary myelofibrosis. We examined the lesions by bronchoscopy, and the biopsy specimen revealed fungus bodies of Cryptococcus with granulomatous inflammation. As a result, the patient was diagnosed with pulmonary cryptococcosis. The patient was treated with fluconazole (200 mg daily for 2 weeks) with concomitant ruxolitinib administration, but the pulmonary lesions progressed. Subsequently, the patient was treated with voriconazole (300 mg daily for 3 weeks), but the lesions worsened further. The administration of ruxolitinib was therefore discontinued, and the dosage of voriconazole was increased to 400 mg daily. Three months later, the pulmonary lesions diminished in size. The present case of pulmonary cryptococcosis occurred in a patient treated with ruxolitinib. Treatment of pulmonary cryptococcosis with concomitant JAK inhibitor administration may result in poor treatment efficacy. It might be better to stop administration of JAK inhibitors, if possible, in patients being treated for pulmonary cryptococcosis. Elsevier 2017-07-04 /pmc/articles/PMC5499110/ /pubmed/28721333 http://dx.doi.org/10.1016/j.rmcr.2017.06.015 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Hirano, Anna Yamasaki, Masahiro Saito, Naomi Iwato, Koji Daido, Wakako Funaishi, Kunihiko Ishiyama, Sayaka Deguchi, Naoko Taniwaki, Masaya Ohashi, Nobuyuki Pulmonary cryptococcosis in a ruxolitinib-treated patient with primary myelofibrosis |
title | Pulmonary cryptococcosis in a ruxolitinib-treated patient with primary myelofibrosis |
title_full | Pulmonary cryptococcosis in a ruxolitinib-treated patient with primary myelofibrosis |
title_fullStr | Pulmonary cryptococcosis in a ruxolitinib-treated patient with primary myelofibrosis |
title_full_unstemmed | Pulmonary cryptococcosis in a ruxolitinib-treated patient with primary myelofibrosis |
title_short | Pulmonary cryptococcosis in a ruxolitinib-treated patient with primary myelofibrosis |
title_sort | pulmonary cryptococcosis in a ruxolitinib-treated patient with primary myelofibrosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499110/ https://www.ncbi.nlm.nih.gov/pubmed/28721333 http://dx.doi.org/10.1016/j.rmcr.2017.06.015 |
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