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Updated: Jun 28, 2026

Microbiological Rapid On-Site Evaluation for Pulmonary Infectious Diseases
Published on: March 1, 2024
[Pneumocystis jiroveci pneumonia during prolonged corticosteroid therapy in an immunocompetent infant]
N Guillemot1, S Blanchon, N Nathan
1Unité de pneumologie pédiatrique, hôpital d'Enfants Armand-Trousseau, AP-HP, 26, avenue du Dr-Netter, 75571 Paris cedex 12, France.
Insights
Pneumocystis jiroveci (PJ) pneumonia is rare in infants but can be severe. This case highlights the risk in immunocompetent infants after prolonged corticosteroid use, emphasizing prompt diagnosis and treatment.
Area of Science:
- Pediatric Pulmonology
- Infectious Diseases
- Immunology
Background:
- Pneumocystis jiroveci (PJ) infection is uncommon in infants and often indicates underlying immunodeficiency.
- Prolonged corticosteroid therapy can increase susceptibility to opportunistic infections, even in seemingly immunocompetent individuals.
Observation:
- A 5.5-month-old infant presented with severe hypoxemic respiratory distress.
- The infant had a history of prolonged oral corticosteroid treatment for a parotid hemangioma.
- Chest X-ray revealed a mixed alveolar-interstitial pattern, and bronchoalveolar lavage confirmed PJ presence.
Findings:
- The infant was diagnosed with severe Pneumocystis jiroveci pneumonia.
- Treatment with intravenous trimethoprim-sulfamethoxazole resulted in a favorable outcome after three weeks.
Implications:
- PJ pneumonia should be suspected in infants with progressive respiratory distress and a mixed alveolar-interstitial pattern on chest imaging.
- Prophylactic therapy is crucial for infants undergoing prolonged immunosuppressive treatments, including chemotherapy and corticosteroid therapy, to prevent severe infections.
Introduction:
Pneumocystis jiroveci (PJ) infection is rare in infants and is suggestive of primary or secondary immunodeficiency. We report on a case of severe PJ pneumonia in an immunocompetent infant after prolonged corticosteroid treatment.
Case Report:
A 5 1/2 month-old girl presented with hypoxemic respiratory distress. Her medical record was remarkable only for a bulky parotid haemangioma, which was treated with prolonged oral corticosteroid therapy. The chest X-ray showed a mixed alveolar-interstitial pattern, and bronchoalveolar lavage revealed the presence of PJ. A favourable outcome was obtained after three weeks of intravenous trimethoprim-sulfamethoxazole treatment.
Conclusion:
PJ infection should be suspected in infants presenting with progressive respiratory distress associated with a mixed alveolar-interstitial pattern. Its potential seriousness justifies prophylactic therapy during prolonged immunosuppressive treatment (chemotherapy, corticosteroid treatment).
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