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Magnetic resonance imaging follow-up of chondroid tumors: regression vs. progression

Authors
Chung, Bo MiHong, Sung HwanYoo, Hye JinChoi, Ja-YoungChae, Hee-DongKim, Dong Hyun
Issue Date
Jun-2018
Publisher
SPRINGER
Keywords
Chondroid tumor; Enchondroma; Regression; MRI
Citation
SKELETAL RADIOLOGY, v.47, no.6, pp 755 - 761
Pages
7
Journal Title
SKELETAL RADIOLOGY
Volume
47
Number
6
Start Page
755
End Page
761
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/71161
DOI
10.1007/s00256-017-2834-z
ISSN
0364-2348
1432-2161
Abstract
Objective To present magnetic resonance imaging (MRI) evidence of the regression or progression of chondroid tumors and to investigate whether MRI can be used to predict the evolution of chondroid tumors. Materials and methods Twenty-one patients with enchondromas or atypical cartilaginous tumors who had undergone extremity MRI at least twice with a minimum 12-month interval between the MRIs were enrolled in this study. The diagnosis was based on the radiography and MRI findings. We classified the tumors into the following three groups according to changes between the MRIs: no change (NC), progression (P), and regression (R). We assessed the initial MRI features, including anatomical location, size, endosteal scalloping, peritumoral edema, fat entrapment, and direction of progression or regression. Nineteen of the 21 patients had contrast-enhanced images, and we analyzed the presence of atypical lobular enhancement against typical peripheral or septal enhancement. Results The R group comprised 11 cases (52%), the P group comprised five cases (24%), and the NC group comprised five cases (24%). None of the MRI features showed statistically significant differences among the groups. Atypical lobular enhancement was observed in the R (6 of 10, 60%) and NC (2 of 5, 40%) groups but not in the P group (0 of 4, 0%), although these differences were not statistically significant. Conclusions Chondroid tumors can either regress or progress in the MRI follow-up. Atypical lobular enhancement was seen only in stable or regressing tumors.
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