Nucl Med Mol Imaging.  2011 Sep;45(3):177-184.

The Clinical Usefulness of 18F-FDG PET/CT in Patients with Systemic Autoimmune Disease

Affiliations
  • 1Department of Nuclear Medicine, Chonnam National University Medical School and Hospital, 8 Hakdong, Dongku, Gwangju 501-757, South Korea. songhc@jnu.ac.kr
  • 2Department of Rheumatology, Chonnam National University Hospital, Gwangju, South Korea.

Abstract

PURPOSE
Individuals with systemic autoimmune disease have an increased susceptibility to both inflammation and malignancy. The aim of this study was to evaluate the clinical usefulness of 18F-FDG PET/CT in patients with systemic autoimmune disease.
METHODS
Forty patients diagnosed with systemic autoimmune disease were enrolled. Diagnostic accuracy of FDG PET/CT for detecting malignancy was assessed. FDG PET/ CT findings, including maximum standardized uptake (SUVmax) of lymphadenopathy (LAP), liver, bone marrow, spleen, joint and muscles, were considered for the characterization of LAPs.
RESULTS
FDG PET/CT could detect metabolically activated lesions in 36 out of 40 patients (90%) including inflammatory lesions in 28 out of 32 patients (88%). The sensitivity, specificity, accuracy, positive predictive value, and negative predictive value of FDG PET/CT for the detection of malignancy were 100, 67, 70, 25, and 100%, respectively. Multiple LAPs were found in 25 of 40 patients (63%), and comprised three malignancies, four cases of tuberculosis, and 18 reactive changes. A SUVmax ratio of bone marrow to liver below 0.78 could distinguish malignancy from tuberculosis + reactive change (AUC=1.000, sensitivity: 100%, specificity: 100%). The SUVmax ratio of spleen to liver in the reactive group was also significantly higher than that in the malignancy group (P=0.014). SUVmax of LAP in the TB group was significantly higher than that in the reactive group (P=0.040).
CONCLUSION
PET/CT is useful in detecting and differentiating inflammation and malignancy in patients with systemic autoimmune disease. Frequent false-positive interpretations can be minimized by consideration of FDG uptake in bone marrow and spleen.

Keyword

Autoimmune disease; PET/CT; Neoplasms; Tuberculosis; Reactive lymphoid hyperplasia

MeSH Terms

Autoimmune Diseases
Bone Marrow
Fluorodeoxyglucose F18
Humans
Inflammation
Joints
Liver
Lymphatic Diseases
Muscles
Pseudolymphoma
Sensitivity and Specificity
Spleen
Tuberculosis
Fluorodeoxyglucose F18
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