Abstract
Pulmonary alveolar proteinosis (PAP) is a rare lung disease characterized by an accumulation of periodic acid-Schiff positive lipoproteinaceous material in the alveolar space. A 67-year-old smoking man was diagnosed with PAP in December 2003. We present the case of PAP with mild and heterogeneous accumulation of F-18 fluorodeoxyglucose (FDG) in both lungs shown on the combined F-18 FDG positron emission tomography and computed tomography. Increased rates of glucose utilization by the inflammatory cells involved in the pathogenesis of PAP might explain the mildly increased pulmonary F-18 FDG uptake we observed.
Original language | English |
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Pages (from-to) | 103-104 |
Number of pages | 2 |
Journal | Clinical Nuclear Medicine |
Volume | 34 |
Issue number | 2 |
DOIs | |
State | Published - 02 2009 |
Externally published | Yes |
Keywords
- F-18 FDG
- Lung
- PET/CT
- Pulmonary alveolar proteinosis