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Choi, B.B., Jee, W.-H., Sunwoo, H.-J., Cho, J.-H., Kim, J.Y., Chun, K.-A., Hong, S.-J., Chung, H. W., Sung, M.-S., Lee, Y.-S. and Chung, Y.-G. (2013) MR Differentiation of Low-Grade Chondrosarcoma from Enchondroma. Clinical Imaging, 37, 542-547.
https://doi.org/10.1016/j.clinimag.2012.08.006

has been cited by the following article:

• TITLE: Enchondromas of Long Bones and Other Skeletal Lesions Found Incidentally Need Critical Evaluation, But Rarely Systematic Follow-Up

  AUTHORS: G. Ulrich Exner, Pascal A. Schai, Nadja Mamisch-Saupe, Michael O. Kurrer

  KEYWORDS: Incidental Bone Lesions, Enchondroma, Fibrous Dysplasia, Non-Ossifying Fibroma

  JOURNAL NAME: Open Journal of Orthopedics, Vol.12 No.2, February 28, 2022

  ABSTRACT: Purpose: Incidental bone lesions are a challenge for the specialist, who has to give recommendations for further management. This review of our cases will assist in the decision whether the lesion can be “neglected”, needs further active follow-up or direct initiation of treatment. Patients and Methods: 153 cases of incidental bone findings were presented to our musculoskeletal tumor service for evaluation from July 2008 through June 2021. 73 of them were cartilaginous tumors and 63 of these were diagnosed as enchondroma of a long bone based on X-Ray and MRI. Results: Follow-up imaging of the enchondroma patients was available for 35 patients at 1 to 13 years (mean 4.3 y), with no change in size except for one femoral diaphyseal enchondroma with increasing diameter from age 18 to 20 years. 14 additional patients answered written contact stating that they remained asymptomatic at 2 to 12 years (mean 5.6 y). None of the patients has been reported to the Swiss Confoederation Cancer Registry to have developed malignancy. Among the 10 other cartilaginous tumors were one chondrosarcoma grade II exhibiting different imaging, 3 non-long-bone localizations (pelvis, scapula and rib), 2 Ollier-type enchondromas, and 2 osteochondromas. Incidental findings other than cartilaginous tumors were fibrous dysplasia (n = 31), non-ossifying fibroma (n = 31) and 18 other “sporadic” entities. Conclusions: Incidentally found enchondromas not exhibiting aggressive features need no systematic follow-up and patients can be “discharged” with the advice to present, if symptoms would develop. This also applies to fibrous dysplasia and the other sporadic lesions. 6 cases with other diagnoses needed specific treatment.