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Published on: March 22, 2012
Fungal pneumonias masquerading as thromboses during induction therapy of acute lymphoblastic leukemia
A D Pearson1, M E Nesbit, P J Darbyshire
1Department of Pediatrics, University of Minnesota, School of Medicine, Minneapolis.
Abstract:
Fatal fungal pneumonias developed in two children with ALL during remission induction. Pulmonary and central nervous system signs suggested the L-asparaginase-induced multiple-thromboses syndrome in both children. Fungal infection should be considered-whenever pneumonia develops in a neutropenic child already receiving broad-spectrum antibiotics or when multiple thromboses occur.
Insights
Fatal fungal pneumonias occurred in two children with acute lymphoblastic leukemia (ALL) during treatment. Symptoms mimicked L-asparaginase-induced thrombosis, highlighting the need to consider fungal infections in neutropenic children.
Area of Science:
- Pediatric Oncology
- Infectious Diseases
- Hematology
Background:
- Acute lymphoblastic leukemia (ALL) treatment often involves immunosuppression.
- Remission induction therapy can lead to neutropenia.
- L-asparaginase is a key chemotherapeutic agent used in ALL treatment.
Observation:
- Two pediatric patients with ALL developed fatal fungal pneumonias during remission induction.
- Clinical signs in both patients suggested L-asparaginase-induced multiple-thromboses syndrome.
- Patients were neutropenic and receiving broad-spectrum antibiotics.
Findings:
- Fungal pneumonia can present with pulmonary and central nervous system symptoms.
- These symptoms can mimic thrombotic events, complicating diagnosis.
- The underlying immunosuppression and L-asparaginase treatment likely contributed to the fungal infections.
Implications:
- Fungal infections should be strongly considered in neutropenic children with ALL experiencing pneumonia.
- The possibility of fungal pneumonia must be evaluated when multiple thromboses occur in this patient population.
- Early recognition and treatment of fungal infections are crucial for improving outcomes in pediatric ALL patients.
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