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Updated: Feb 14, 2026

Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma
Published on: April 11, 2018
Whole-tumor apparent diffusion coefficient (ADC) histogram analysis to differentiate benign peripheral neurogenic
Masanori Nakajo1, Yoshihiko Fukukura1, Hiroto Hakamada1
1Department of Radiology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Background:
Apparent diffusion coefficient (ADC) histogram analyses have been used to differentiate tumor grades and predict therapeutic responses in various anatomic sites with moderate success.
Purpose:
To determine the ability of diffusion-weighted imaging (DWI) with a whole-tumor ADC histogram analysis to differentiate benign peripheral neurogenic tumors (BPNTs) from soft tissue sarcomas (STSs).
Study Type:
Retrospective study, single institution.
Subjects:
In all, 25 BPNTs and 31 STSs.
Field Strength/Sequence:
Two-b value DWI (b-values = 0, 1000s/mm2 ) was at 3.0T.
Assessment:
The histogram parameters of whole-tumor for ADC were calculated by two radiologists and compared between BPNTs and STSs.
Statistical Tests:
Nonparametric tests were performed for comparisons between BPNTs and STSs. P < 0.05 was considered statistically significant. The ability of each parameter to differentiate STSs from BPNTs was evaluated using area under the curve (AUC) values derived from a receiver operating characteristic curve analysis.
Results:
The mean ADC and all percentile parameters were significantly lower in STSs than in BPNTs (P < 0.001-0.009), with AUCs of 0.703-0.773. However, the coefficient of variation (P = 0.020 and AUC = 0.682) and skewness (P = 0.012 and AUC = 0.697) were significantly higher in STSs than in BPNTs. Kurtosis (P = 0.295) and entropy (P = 0.604) did not differ significantly between BPNTs and STSs.
Data Conclusion:
Whole-tumor ADC histogram parameters except kurtosis and entropy differed significantly between BPNTs and STSs.
Level Of Evidence:
3 Technical Efficacy: Stage 2 J. Magn. Reson. Imaging 2018.
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