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Apparent diffusion coefficient (ADC): A potential in vivo biological surrogate of the incidentally discovered bone lesions at 3T MRI
PURPOSE: To probe the potential of apparent diffusion coefficient (ADC) to rectify the incidentally detected bone lesion on MRI into benign or malignant lesions. MATERIALS AND METHODS: We retrospectively recruited 44 patients (24 males and 20 females); with 52 bone lesions, who underwent diffusion w...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628214/ https://www.ncbi.nlm.nih.gov/pubmed/34877369 http://dx.doi.org/10.1016/j.ejro.2021.100386 |
Sumario: | PURPOSE: To probe the potential of apparent diffusion coefficient (ADC) to rectify the incidentally detected bone lesion on MRI into benign or malignant lesions. MATERIALS AND METHODS: We retrospectively recruited 44 patients (24 males and 20 females); with 52 bone lesions, who underwent diffusion weighted (DW) imaging using multiple b-values on 3 T MRI. ADC maps were derived and analyzed by two radiologists; blinded to the final diagnosis. The mean ADC values were used for statistical analyses. The diagnosis was deduced by histopathological confirmation; in 32 lesions and strict clinical and imaging follow-up for at least 12 months; in 20 lesions. RESULTS: The mean ADC value (mean±SD) of all malignant tumors (including cartilaginous neoplasms) was [0.92 ± 0.40] × 10ˉ3 mm(2)/s. This significantly differed from those of both primary benign tumors [1.14 ± 0.24] × 10ˉ3 mm(2)/s, (p = 0.011), and all non-malignant lesions collectively [1.29 ± 0.44] × 10ˉ3 mm(2)/s, (p < 0.001). Using mADC value of ≤ 1.1 × 10ˉ(3) mm(2)/s resulted in 86.1% sensitivity and 62.5% specificity for characterizing a lesion as a malignant. The inter-rater reliability was almost perfect (95% CI = 0.954–0.985). CONCLUSION: ADC could be a non-invasive in-vivo surrogate that may be able to discern the incidentally discovered osseous lesions into benign and malignant pathologies and guide further diagnostic workup. |
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