Extracorporeal Membrane Oxygenation for Pneumocystis jirovecii Pneumonia in a Child With Multisystem Langerhans Cell Histiocytosis.

J Pediatr Hematol OncolJul 14, 2026 (epub)

Vivek Mohan, Sanjay Kumar, Akashneel Bhattacharya et al.

✦ AI-curated · Sources linked

Case in brief

A 3-year-old boy with multisystem Langerhans cell histiocytosis developed severe Pneumocystis jirovecii pneumonia during treatment. Despite high-dose trimethoprim-sulfamethoxazole and invasive mechanical ventilation, he experienced refractory respiratory failure. Venovenous ECMO was initiated, leading to rapid improvement in gas exchange, decannulation by day 6, and extubation by day 8. The child completed treatment and remains well at 10-month follow-up.

Diagnostic / clinical pearl

Early recognition and aggressive supportive care are crucial in managing severe Pneumocystis jirovecii pneumonia, especially in immunocompromised children.

Why it matters

This case highlights the potential role of venovenous ECMO as a lifesaving intervention in selected patients with isolated respiratory failure due to PJP.

Source

Published in J Pediatr Hematol Oncol. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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