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The Quarterly Journal of Nuclear Medicine and Molecular imaging 2010 December;54(6):698-703
Copyright © 2011 EDIZIONI MINERVA MEDICA
language: English
FDG uptake in lymph-nodes of HIV+ and tuberculosis patients: implications for cancer staging
Sathekge M. 1, Maes A. 2, 3, Kgomo M. 4, Pottel H. 5, Stolz A. 6, Van De Wiele C. 7 ✉
1 Department of Nuclear Medicine, University of Pretoria, Pretoria, South-africa; 2 Department of Internal Medicine, Louis Pasture Hospital, Pretoria, South-Africa; 3 Department of Infectious Diseases, University of Pretoria, Pretoria, South-Africa; 4 Department of Nuclear Medicine, AZ Groeninge, Kortrijk, Belgium; 5 Department of Morphology and Medical Imaging, University Hospital Leuven, Leuven, Belgium; 6 Subfaculty of Medicine, Catholic University Leuven, Campus Kortrijk, Belgium 7 Department of Nuclear Medicine University Hospital Ghent, Ghent, Belgium
AIM: The incidence of non-AIDS-related cancers (NADCs) in the AIDS-population has surpassed that of the general population. HIV significantly increases an individual’s chances of reactivation of latent tuberculosis (TB) infection and progression to active TB disease. Both HIV, TB and CA present with increased FDG uptake in involved lymph nodes (LNs). The aim of this study was to assess the existence of quantitative differences in FDG uptake by lymph nodes in HIV+/TB-/CA- patients, TB+/HIV-/CA-, TB+/HIV+/CA- patients and HIV-/TB-/CA+ patients.
METHODS: Sixteen consecutive referred patients suffering from HIV-1, 21 suffering from HIV-1 and TB and 16 suffering from TB alone were prospectively included. In addition, 30 consecutively referred, previously untreated, HIV and TB negative cancer patients were included. All patients underwent FDG PET imaging. Mean standardized uptake values (SUV mean values) were obtained for involved lymph nodes using region growing and a threshold of 30% in all patients. Results obtained were compared using non-parametric statistics.
RESULTS: SUVmean values of involved LNs of HIV+/TB+/CA- patients were significantly higher than SUVmean values of involved LNs of HIV-/TB+/CA- patients and HIV+/TB-/CA patients (P<0.05). Also, SUVmean values of involved LNs of HIV-/TB-/CA+ patients were significantly higher than SUVmean values of involved LNs of HIV+/TB-/CA- patients. HIV+/TB+/CA- patients presented with a significantly higher number of sites of LN involvement when compared to the HIV+/TB-/CA- patient group.
CONCLUSION: FDG PET is not useful for assessing malignant lymph node involvement in HIV+, TB+ or HIV+/TB+ patients.