A Case of Interstitial Lung Disease Probably Related to Rituximab Treatment
A 44-year-old male developed interstitial lung disease (ILD) during treatment with rituximab (375 mg/m 2 weekly intravenous × 4 weeks) for the management of immune thrombocytopenia (ITP). After 1 month of treatment he developed dyspnea, fever (38.9 °C), an increase of C-reactive protein (CRP) and wh...
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Published in: | Drug safety - case reports Vol. 2; no. 1 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Cham
Springer International Publishing
01-12-2015
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Subjects: | |
Online Access: | Get full text |
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Summary: | A 44-year-old male developed interstitial lung disease (ILD) during treatment with rituximab (375 mg/m
2
weekly intravenous × 4 weeks) for the management of immune thrombocytopenia (ITP). After 1 month of treatment he developed dyspnea, fever (38.9 °C), an increase of C-reactive protein (CRP) and white blood cells with hypoxemia, and decreased platelets. Chest X-ray and high-resolution computed tomography revealed diffuse bilateral lung infiltrates. He was diagnosed with severe ILD; rituximab was discontinued, and treatment with fluticasone combined with salmeterol, methylprednisolone, and omeprazole was started, with an improvement of symptoms over 15 days with normalization in CRP at 30 days. A Naranjo assessment score of 6 was obtained, indicating a probable relationship between the patient’s symptoms and the suspect drug. In conclusion, in ITP patients treated with rituximab, we suggest evaluating pulmonary endpoints through pharmaco-epidemiological observational studies. |
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ISSN: | 2199-1162 2198-977X |
DOI: | 10.1007/s40800-015-0010-8 |