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Use of FDG-PET in differentiating benign from malignant compression fractures

OBJECTIVE: The objective was to evaluate the use of fluorodeoxyglucose positron emission tomography (FDG-PET) in differentiating benign from malignant compression fractures. PATIENTS AND METHODS: In a retrospective analysis, we identified 33 patients with 43 compression fractures who underwent FDG-P...

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Autores principales: Bredella, Miriam A., Essary, Brendan, Torriani, Martin, Ouellette, Hugue A., Palmer, William E.
Formato: Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2271083/
https://www.ncbi.nlm.nih.gov/pubmed/18278491
http://dx.doi.org/10.1007/s00256-008-0452-5
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author Bredella, Miriam A.
Essary, Brendan
Torriani, Martin
Ouellette, Hugue A.
Palmer, William E.
author_facet Bredella, Miriam A.
Essary, Brendan
Torriani, Martin
Ouellette, Hugue A.
Palmer, William E.
author_sort Bredella, Miriam A.
collection PubMed
description OBJECTIVE: The objective was to evaluate the use of fluorodeoxyglucose positron emission tomography (FDG-PET) in differentiating benign from malignant compression fractures. PATIENTS AND METHODS: In a retrospective analysis, we identified 33 patients with 43 compression fractures who underwent FDG-PET. On FDG-PET the uptake pattern was recorded qualitatively and semiquantitatively and fractures were categorized as benign or malignant. Standardized uptake values (SUV) were obtained. MRI, CT, and biopsy results as well as clinical follow-up for 1–3 years served as standards of reference. The Student’s t test was used to determine whether there was a statistically significant difference between the SUV for benign and malignant compression fractures. RESULTS: There were 14 malignant and 29 benign compression fractures, including 5 acute benign fractures. On FDG-PET, 5 benign fractures were falsely classified as malignant (false-positive). Three of these patients underwent prior treatment with bone marrow-stimulating agents. There were two false-negative results. Sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of FDG-PET in differentiating benign from malignant compression fractures were 86%, 83%, 84%, 71%, and 92% respectively. The difference between SUV values of benign and malignant fractures was statistically significant (1.9 ± 0.97 for benign and 3.9 ± 1.52 for malignant fractures, p < 0.001). SUV of benign acute and chronic fractures were not statistically significant. CONCLUSION: Fluorodeoxyglucose positron emission tomography is useful in differentiating benign from malignant compression fractures. Therapy with bone marrow-stimulating agents can mimic malignant involvement.
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spelling pubmed-22710832008-03-25 Use of FDG-PET in differentiating benign from malignant compression fractures Bredella, Miriam A. Essary, Brendan Torriani, Martin Ouellette, Hugue A. Palmer, William E. Skeletal Radiol Scientific Article OBJECTIVE: The objective was to evaluate the use of fluorodeoxyglucose positron emission tomography (FDG-PET) in differentiating benign from malignant compression fractures. PATIENTS AND METHODS: In a retrospective analysis, we identified 33 patients with 43 compression fractures who underwent FDG-PET. On FDG-PET the uptake pattern was recorded qualitatively and semiquantitatively and fractures were categorized as benign or malignant. Standardized uptake values (SUV) were obtained. MRI, CT, and biopsy results as well as clinical follow-up for 1–3 years served as standards of reference. The Student’s t test was used to determine whether there was a statistically significant difference between the SUV for benign and malignant compression fractures. RESULTS: There were 14 malignant and 29 benign compression fractures, including 5 acute benign fractures. On FDG-PET, 5 benign fractures were falsely classified as malignant (false-positive). Three of these patients underwent prior treatment with bone marrow-stimulating agents. There were two false-negative results. Sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of FDG-PET in differentiating benign from malignant compression fractures were 86%, 83%, 84%, 71%, and 92% respectively. The difference between SUV values of benign and malignant fractures was statistically significant (1.9 ± 0.97 for benign and 3.9 ± 1.52 for malignant fractures, p < 0.001). SUV of benign acute and chronic fractures were not statistically significant. CONCLUSION: Fluorodeoxyglucose positron emission tomography is useful in differentiating benign from malignant compression fractures. Therapy with bone marrow-stimulating agents can mimic malignant involvement. Springer Berlin Heidelberg 2008-05-01 2008 /pmc/articles/PMC2271083/ /pubmed/18278491 http://dx.doi.org/10.1007/s00256-008-0452-5 Text en © ISS 2008 This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Scientific Article
Bredella, Miriam A.
Essary, Brendan
Torriani, Martin
Ouellette, Hugue A.
Palmer, William E.
Use of FDG-PET in differentiating benign from malignant compression fractures
title Use of FDG-PET in differentiating benign from malignant compression fractures
title_full Use of FDG-PET in differentiating benign from malignant compression fractures
title_fullStr Use of FDG-PET in differentiating benign from malignant compression fractures
title_full_unstemmed Use of FDG-PET in differentiating benign from malignant compression fractures
title_short Use of FDG-PET in differentiating benign from malignant compression fractures
title_sort use of fdg-pet in differentiating benign from malignant compression fractures
topic Scientific Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2271083/
https://www.ncbi.nlm.nih.gov/pubmed/18278491
http://dx.doi.org/10.1007/s00256-008-0452-5
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