RSNA 2006 

Abstract Archives of the RSNA, 2006


LL-MK4291-H06

Application Study of Musculoskeletal Tumors with Combined Multifunctional MR Methods

Scientific Posters

Presented on November 28, 2006
Presented as part of LLMK-H: Musculoskeletal

Participants

Zi-hua Qi PhD, Presenter: Nothing to Disclose
Chuan-fu Li, Abstract Co-Author: Nothing to Disclose

PURPOSE

To study the significance of benign and malignant musculoskeletal tumors using multi-functional MR methods including dynamic contrast-enhanced MRI(MR-DCE), diffusion-weighted imaging(DWI), 31P-MRS and 1H-MRS.

METHOD AND MATERIALS

Four MR methods were carried out in 33 patients with musculoskeletal tumors. The functional MR parameters were evaluated including time-signal intensity curve(TIC), maximum slope of increase(MSI), maximum slope of decrease(MSD), positive enhancement integral (PEI), signal enhancement ratio(SER), peak time(PT), intracellular pH value (pHi), phosphomonoester (PME), phosphodiester (PDE), phosphocreatine(PCr), inorganic phosphate (Pi)、β-ATP, and the ratios of PCr/PME, PME/NTP and PME/ATP, choline, creatine, apparent diffusion cofficient(ADC) and exponential apparent diffusion cofficient(eADC).

RESULTS

Most lesions with type ⅠorⅡ of TIC were malignant, and using these types as a standard of malignancy, the diagnostic sensitivity, specificity and accuracy was 92.00%, 70.59% and 83.33% respectively. There was a significance of the types of TIC between benign and malignant tumors(PP=0.003). MSI and MSD of metastasis were higher than those of benign tumors (PPP2(P<0.05), while the eADC is opposite.

CONCLUSION

Combined multi-functional MR methods may get more information and help to improve diagnosis of musculoskeletal tumors.

CLINICAL RELEVANCE/APPLICATION

Multi-functional MR methods may provide more information, and can be recommended to verify diagnostic efficacy.

Cite This Abstract

Qi, Z, Li, C, Application Study of Musculoskeletal Tumors with Combined Multifunctional MR Methods.  Radiological Society of North America 2006 Scientific Assembly and Annual Meeting, November 26 - December 1, 2006 ,Chicago IL. http://archive.rsna.org/2006/4433766.html