Cannon Christopher P, Nelson Scott D, Seeger Leanne L, Eckardt Jeffrey J
Department of Orthopaedic Surgery, Madigan Army Medical Center, Ft. Lewis, WA 98431-5000, USA.
Skeletal Radiol. 2002 Jun;31(6):369-72. doi: 10.1007/s00256-002-0519-7. Epub 2002 May 3.
We report the case of a clear cell chondrosarcoma (CCCS) occurring in the femoral head of a 14-year-old skeletally immature boy. Radiographic examination revealed a well-defined, osteolytic lesion in the epiphysis of the femoral head. Given the patient's age and the radiographic appearance of the lesion, chondroblastoma was high on the differential diagnosis. A frozen section was performed at the time of open biopsy was felt to be consistent with either chondroblastoma or CCCS. CCCS in a skeletally immature patient was felt to be unlikely, so curettage and bone grafting was performed. Final pathology review, however, confirmed the diagnosis of CCCS. The patient was taken back to surgery 4 weeks later for a wide resection and hemiarthroplasty.
我们报告了一例发生在一名14岁骨骼未成熟男孩股骨头的透明细胞软骨肉瘤(CCCS)病例。影像学检查显示股骨头骨骺有一个边界清晰的溶骨性病变。鉴于患者的年龄和病变的影像学表现,软骨母细胞瘤在鉴别诊断中可能性较大。在进行切开活检时做了冰冻切片,结果被认为与软骨母细胞瘤或CCCS相符。考虑到骨骼未成熟患者发生CCCS的可能性不大,因此进行了刮除术和骨移植。然而,最终病理检查确诊为CCCS。4周后患者再次接受手术,进行了广泛切除和半关节置换术。