Affiliation:
1. Radiology
2. Pathology
3. Orthopaedic Surgery, Teikyo University School of Medicine
4. Department of Diagnostic Pathology, National Cancer Center Hospital, Tokyo, Japan.
Abstract
Abstract
We present a new, extremely rare nonmyxoid cellular variant of extraskeletal myxoid chondrosarcoma. Although diagnosis is radiologically and pathologically challenging, FDG PET/CT and MRI accurately showed the malignancy and high tumor density. A 52-year-old woman complained of a left dorsal mass, which presented inhomogeneous intermediate signals on T2-weighted images, with diffusion restriction, strong enhancement, and increased accumulation of FDG (SUVmax, 5.2). Although biopsy was inconclusive, a highly malignant tumor was suspected radiologically. The resected specimen was histologically diagnosed as extraskeletal myxoid chondrosarcoma by detection of EWSR1::NR4A3 fusion using fluorescence in situ hybridization.
Publisher
Ovid Technologies (Wolters Kluwer Health)