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Extracorporeal Membrane Oxygenation for Pneumocystis jirovecii Pneumonia in a Child With Multisystem Langerhans Cell
Vivek Mohan1, Sanjay Kumar2, Akashneel Bhattacharya3
1Department of Hematology and Bone Marrow Transplant, Artemis Hospital.
Insights
Extracorporeal membrane oxygenation (ECMO) can be a life-saving intervention for children with severe Pneumocystis jirovecii pneumonia (PJP) and acute respiratory distress syndrome (ARDS). Timely V-V ECMO initiation facilitated recovery in a pediatric case of PJP.
Area of Science:
- Pediatric critical care medicine
- Infectious diseases
- Pulmonology
Background:
- Pneumocystis jirovecii pneumonia (PJP) is a severe opportunistic infection in immunocompromised children, often leading to fatal outcomes when progressing to acute respiratory distress syndrome (ARDS).
- The use of extracorporeal membrane oxygenation (ECMO) for PJP-induced ARDS in pediatric patients is not well-established, with limited case reports available.
Purpose of the Study:
- To present a case of severe PJP in a pediatric patient with multisystem Langerhans cell histiocytosis.
- To highlight the successful application of venovenous (V-V) ECMO as a rescue therapy for refractory respiratory failure secondary to PJP.
Main Methods:
- A 3-year-old boy with multisystem Langerhans cell histiocytosis on chemotherapy developed severe PJP with respiratory failure.
- Despite maximal medical management including mechanical ventilation, venovenous (V-V) ECMO was initiated for rescue support.
- Bronchoalveolar lavage confirmed Pneumocystis jirovecii and Klebsiella pneumoniae co-infection.
Main Results:
- The patient showed rapid improvement in gas exchange after V-V ECMO initiation, allowing for decannulation on day 6 and extubation by day 8.
- Radiographic resolution of pneumonia was observed within 2 weeks.
- The child completed treatment, resumed chemotherapy, and remained well at 10-month follow-up with secondary PJP prophylaxis.
Conclusions:
- Early recognition and aggressive supportive care are crucial for managing severe PJP in immunocompromised children.
- In select pediatric patients with isolated, reversible respiratory failure, timely V-V ECMO can be a life-saving measure.
- V-V ECMO can facilitate patient recovery while definitive antimicrobial therapy is administered.
Background:
Pneumocystis jirovecii pneumonia (PJP) is a rapidly progressive and potentially fatal opportunistic infection in non-HIV immunocompromised children. Mortality is particularly high when PJP progresses to acute respiratory distress syndrome (ARDS). The role of extracorporeal membrane oxygenation (ECMO) in this setting remains limited to select reports.
Case Presentation:
We report a 3-year-old boy with multisystem Langerhans cell histiocytosis receiving vinblastine and corticosteroids who developed severe PJP during consolidation therapy. Despite early initiation of high-dose trimethoprim-sulfamethoxazole, adjunctive corticosteroids, and escalation to invasive mechanical ventilation, he developed refractory hypoxemic and hypercapnic respiratory failure. Bronchoalveolar lavage multiplex polymerase chain reaction confirmed Pneumocystis jirovecii with concurrent Klebsiella pneumoniae . In the absence of hemodynamic compromise or multiorgan dysfunction, venovenous (V-V) ECMO was initiated as rescue support. Rapid improvement in gas exchange allowed decannulation on day 6 and extubation by day 8. Radiologic resolution occurred within 2 weeks. The child completed antimicrobial therapy, resumed maintenance chemotherapy, and remains well at 10-month follow-up on secondary PJP prophylaxis.
Conclusion:
This case underscores the importance of early recognition and aggressive supportive care. In selected patients with isolated, potentially reversible respiratory failure, timely initiation of V-V ECMO can be lifesaving and may facilitate recovery while definitive antimicrobial therapy takes effect.