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a Divisions of
Immunology/ Haematology/Oncology/ BMT and Infectious Diseases,
University Children's Hospital, Zürich, Switzerland, b Division of Paediatric Radiology, University
Children's Hospital, c Department of Radiology, Division of Nuclear
Medicine, University Hospital, Zürich, Switzerland
Correspondence to: Dr Güngör Tayfun.Guengoer{at}kispi.unizh.ch
Accepted 11 June
2001
AIMS
To compare whole body positron
emission tomography (PET) using
fluorine-18-fluoro-2-deoxy-D-glucose (FDG) with computed
tomography (CT) in detecting active infective foci in children with
chronic granulomatous disease.
METHODS
We performed 22 whole body
FDG PET studies in seven children with X linked (n = 6) or autosomal
recessive (n = 1) CGD. All had clinical signs of infection and/or
were evaluated prior to bone marrow transplantation (BMT). Nineteen PET
studies were also correlated with chest and/or abdominal CT. All PET
scans were interpreted blinded to the CT findings. Diagnoses were
confirmed histologically and bacteriologically.
RESULTS
We detected 116 lesions in
22 FGD PETs and 126 lesions on 19 CTs. Only two of the latter could be
classified reliably as active lesions by virtue of contrast enhancement
suggesting abscess formation. PET excluded 59 lesions suspicious for
active infection on CT and revealed 49 infective lesions not seen on
CT. All seven active infective lesions were identified by PET, allowing
targeted biopsy and identification of the infective agent followed by
specific antimicrobial treatment, surgery, or subsequent BMT.
CONCLUSIONS
Identification of
infective organisms is more precise if active lesions are biopsied. CT
does not discriminate between active and inactive lesions. Whole body
FDG PET can be used to screen for active infective lesions in CGD patients.
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