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Fever and Cough in Methotrexate-treated Patients: An Approach
1Departments of Pulmonary and Critical Care Medicine (L.S.A.) and Rheumatic and Immunologic Diseases (J.M.C.), Cleveland Clinic Foundation, Cleveland, Ohio.
Abstract:
The prevalence of acute methotrexate pneumonitis is up to 5.5%. Its presentation is often difficult to distinguish from opportunistic infections such as Pneumocystis carinii, nocardia, and cryptococcus or from interstitial infiltrates from the underlying rheumatic disease. Its recognition rests on the presence of cough, dyspnea, fever, new pulmonary function test abnormalities, and acute infiltrates on chest radiograph. The diagnosis ultimately rests on histologic confirmation and exclusion of infection. Bronchoalveolar lavage for cultures, and special staining of lavage and transbronchial histopathology specimens, often allows identification of opportunistic pathogens. Transbronchial biopsy may provide sufficient material for the diagnosis of either methotrexate pneumonitis of rheumatoid lung, particularly when correlated with the clinical presentation. Open lung biopsy should be considered if a diagnosis cannot be obtained on bronchoscopy. Despite a mortality of up to 10%, methotrexate pneumonitis usually responds to discontinuation of the drug and trial of corticosteroids.
Insights
Acute methotrexate pneumonitis, a lung condition affecting up to 5.5% of patients, presents with cough, fever, and infiltrates. Diagnosis requires excluding infection and confirming with histology, often responding to corticosteroids.
Area of Science:
- Pulmonology
- Rheumatology
- Pharmacology
Background:
- Acute methotrexate pneumonitis (AMP) affects up to 5.5% of patients treated with methotrexate.
- AMP symptoms like cough, dyspnea, and fever can mimic opportunistic infections or underlying rheumatic disease infiltrates.
- Accurate diagnosis is crucial for appropriate management and to prevent severe outcomes.
Purpose of the Study:
- To outline the diagnostic criteria for acute methotrexate pneumonitis.
- To emphasize the importance of differentiating AMP from other pulmonary conditions.
- To discuss diagnostic methods and treatment strategies for AMP.
Main Methods:
- Clinical presentation review including cough, dyspnea, fever, pulmonary function tests, and chest radiograph findings.
- Diagnostic confirmation through exclusion of infection and histologic evidence.
- Utilizing bronchoalveolar lavage (BAL) for cultures and special stains.
- Employing transbronchial biopsy and considering open lung biopsy when necessary.
Main Results:
- Recognition of AMP relies on characteristic clinical symptoms, new pulmonary function abnormalities, and acute radiographic infiltrates.
- Histologic confirmation and exclusion of infection are essential for definitive diagnosis.
- BAL and transbronchial biopsies can identify opportunistic pathogens and provide diagnostic material.
- Open lung biopsy is reserved for cases undiagnosed by bronchoscopy.
Conclusions:
- Acute methotrexate pneumonitis requires a high index of suspicion and a systematic diagnostic approach.
- Prompt diagnosis and treatment, including drug discontinuation and corticosteroid therapy, can lead to favorable outcomes.
- Despite a potential mortality of up to 10%, AMP is often responsive to treatment, highlighting the importance of early recognition.
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