Martel Villagrán J, Bueno Horcajadas Á, Pérez Fernández E, Martín Martín S
Departamento de Diagnóstico por Imagen, Hospital Universitario Fundación Alcorcón, Alcorcón, España.
Departamento de Diagnóstico por Imagen, Hospital Universitario Fundación Alcorcón, Alcorcón, España.
Radiologia. 2015 Mar-Apr;57(2):142-9. doi: 10.1016/j.rx.2013.11.003. Epub 2014 Apr 24.
To determine the ability of MRI to distinguish between benign and malignant vertebral lesions.
We included 85 patients and studied a total of 213 vertebrae (both pathologic and normal). For each vertebra, we determined whether the lesion was hypointense in T1-weighted sequences and whether it was hyperintense in STIR and in diffusion-weighted sequences. We calculated the in-phase/out-of-phase quotient and the apparent diffusion coefficient for each vertebra. We combined parameters from T1-weighted, diffusion-weighted, and STIR sequences to devise a formula to distinguish benign from malignant lesions.
The group comprised 60 (70.6%) women and 25 (29.4%) men with a mean age of 67±13.5 years (range, 33-90 y). Of the 85 patients, 26 (30.6%) had a known primary tumor. When the lesion was hypointense on T1-weighted sequences, hyperintense on STIR and diffusion-weighted sequences, and had a signal intensity quotient greater than 0.8, the sensitivity was 97.2%, the specificity was 90%, and the diagnostic accuracy was 91.2%. If the patient had a known primary tumor, these values increased to 97.2%, 99.4%, and 99%, respectively.
Benign lesions can be distinguished from malignant lesions if we combine the information from T1-weighted, STIR, and diffusion-weighted sequences together with the in-phase/out-of-phase quotient of the lesion detected in the vertebral body on MRI.