Pneumocystis pneumonia in a patient with rheumatoid arthritis treated with methotrexate: A case report

Rationale: Pneumocystis jirovecii pneumonia (PCP) is an opportunistic and life-threatening pulmonary infection observed in patients receiving immunosuppressive treatment. In rheumatoid arthritis (RA) patients, methotrexate (MTX) is a risk factor for PCP. However, it is difficult to clinically differentiate between RA-related interstitial pneumonia, MTX-related interstitial pneumonia, and PCP. Patients concerns: An 88-year-old Japanese woman with a 4 years history of RA was admitted to our hospital with shortness of breath. She was initially treated with salazosulfapyridine (1000 mg/day). However, her active arthritis had been refractory and she was treated with MTX (8 mg/week) at 20 months before current presentation. Diagnosis: High-resolution chest computed tomography demonstrated diffuse ground-glass opacities distributed throughout the middle and lower lobes, predominantly in the right lung. Although serum β-D-glucan (BDG) level was low, the patient was clinically diagnosed with PCP based on the positive result in polymerase chain reaction for P. jirovecii DNA using the sputum sample. Intervention: The patient was immediately treated with trimethoprim–sulfamethoxazole and high-dose prednisolone, which successfully improved pulmonary shadows and respiratory failure. Outcomes: The patient’s respiratory symptoms including hypoxia improved. On day 11, the patient developed trunk pruritus and rashes, prompting a transition from trimethoprim/sulfamethoxazole to atovaquone. On day 14, chest CT showed complete resolution of the ground-glass opacities. The patient was discharged from our hospital on the 21th day. Lessons: Evidence regarding the diagnostic testing for PCP in patients with RA is insufficient. Measurement of BDG levels is useful for the early diagnosis of PCP in human immunodeficiency virus-infected patients. However, BDG levels should be carefully judged when PCP is suspected in RA patients receiving MTX. Progressive respiratory distress should be considered to be a consequence of PCP, and physicians should consider establishing an early diagnosis and treatment intervention for PCP in patients with RA receiving MTX.

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Journal
Medicine Case Reports and Study Protocols
Published
2025-07-18
DOI
https://doi.org/10.1097/md9.0000000000000371
Primary Topic
Pneumocystis jirovecii pneumonia detection and treatment
Type
article
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article

Pneumocystis pneumonia in a patient with rheumatoid arthritis treated with methotrexate: A case report

Shuzo Sato, Kokushi Yamasaki, Hiroki Yamane, Kiyoshi Migita et al.
Medicine Case Reports and Study Protocols
Pneumocystis jirovecii pneumonia detection and treatment
article

Pneumocystis pneumonia in a patient with rheumatoid arthritis treated with methotrexate: A case report

Shuzo Sato, Kokushi Yamasaki, Hiroki Yamane, Kiyoshi Migita, Haruki Matsumoto, Sosuke Tsuji, Satoru Fujino, A. Kawakami, Reiji Nakano, Fumi Mori, Ichiro Isomoto
article en

Abstract

Rationale: Pneumocystis jirovecii pneumonia (PCP) is an opportunistic and life-threatening pulmonary infection observed in patients receiving immunosuppressive treatment. In rheumatoid arthritis (RA) patients, methotrexate (MTX) is a risk factor for PCP. However, it is difficult to clinically differentiate between RA-related interstitial pneumonia, MTX-related interstitial pneumonia, and PCP. Patients concerns: An 88-year-old Japanese woman with a 4 years history of RA was admitted to our hospital with shortness of breath. She was initially treated with salazosulfapyridine (1000 mg/day). However, her active arthritis had been refractory and she was treated with MTX (8 mg/week) at 20 months before current presentation. Diagnosis: High-resolution chest computed tomography demonstrated diffuse ground-glass opacities distributed throughout the middle and lower lobes, predominantly in the right lung. Although serum β-D-glucan (BDG) level was low, the patient was clinically diagnosed with PCP based on the positive result in polymerase chain reaction for P. jirovecii DNA using the sputum sample. Intervention: The patient was immediately treated with trimethoprim–sulfamethoxazole and high-dose prednisolone, which successfully improved pulmonary shadows and respiratory failure. Outcomes: The patient’s respiratory symptoms including hypoxia improved. On day 11, the patient developed trunk pruritus and rashes, prompting a transition from trimethoprim/sulfamethoxazole to atovaquone. On day 14, chest CT showed complete resolution of the ground-glass opacities. The patient was discharged from our hospital on the 21th day. Lessons: Evidence regarding the diagnostic testing for PCP in patients with RA is insufficient. Measurement of BDG levels is useful for the early diagnosis of PCP in human immunodeficiency virus-infected patients. However, BDG levels should be carefully judged when PCP is suspected in RA patients receiving MTX. Progressive respiratory distress should be considered to be a consequence of PCP, and physicians should consider establishing an early diagnosis and treatment intervention for PCP in patients with RA receiving MTX.

Medicine Case Reports and Study ProtocolsVol. 6(4)
Fukushima Medical University (JP), Nagasaki Medical Center (JP), St. Francis Hospital (US), Nagasaki University (JP)
Good health and well-being
Openalex Percentile: Top 72%
Pneumocystis jirovecii pneumonia detection and treatment
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