Abstract
A 64-year-old man was diagnosed with acute myeloid leukemia (AML) 5 years following single lung transplantation performed for severe pulmonary hypertension from scleroderma. Chemotherapy for treatment of AML with fludarabine, cytosine arabinoside, G-CSF (FLAG) regimen was initiated. Despite intensive antibiotic treatment for a presumptive diagnosis of bacterial pneumonia, the patient developed acute respiratory failure and died before a complete cycle of chemotherapy could be administered. At autopsy, both native and allograft lungs showed widespread alveolar proteinosis that was determined as the main cause of acute respiratory failure. Alveolar proteinosis, a potentially treatable disease, should be considered in the radiologic differential diagnosis of diffuse lung disease in this clinical setting.
Original language | English (US) |
---|---|
Pages (from-to) | 307-309 |
Number of pages | 3 |
Journal | Journal of Thoracic Imaging |
Volume | 16 |
Issue number | 4 |
DOIs | |
State | Published - Nov 20 2001 |
Keywords
- Acute myeloid leukemia
- Chemotherapy
- FLAG
- Lung transplantation
- Pulmonary alveolar proteinosis
ASJC Scopus subject areas
- Radiology Nuclear Medicine and imaging
- Pulmonary and Respiratory Medicine