摘要
本文回顾分析362例骨巨细胞瘤中38例发生于青少年的X线表现,其发病年龄均在20岁以下。其中26例位于短和长管状骨,22例的骨骺线尚未闭合,均未侵犯骨骺。所有病变均表现为溶骨性破坏,9例的皮质呈不规则破坏。36例均有膨胀使新的皮质骨重新塑形形成其外缘。28例病理分级属于Ⅰ级和Ⅱ级,19例属Ⅲ级,Ⅳ级仅1例。属于Ⅰ级和Ⅱ级的28例中除2例外均在X线片上表现为良性,Ⅲ级和Ⅳ级的10例中,X线片看到恶性征象者仅3例。
The radiological appearance of giant cell tumor in the developing skeleton was retrospectively assessd in 38(10.5%) in 362 patients,There were all under the age of 20.26 tumors were located in short and long tubular bones with epiphyseal growth plates still open in 22 patients,the epiphysis were never involved.All lesions showed a osteolytic type of destruction;the cortex was irregularly destroyed in 9 cases,Expansile remodling of a neocortex was present in 36 patients.Most of this group patients(28 cases) had lesion of grade Ⅰand Ⅱ, 9 lesions were grade Ⅲ, and only 1 lesion was grade Ⅳ. 28 patients which had lesions of grade Ⅰ and Ⅱ, except 2 patients,all considered radiologically benign;in 10 cases of grade Ⅲ and Ⅳ,the radiological appearance were malignant only 3 cases.
出处
《临床放射学杂志》
CSCD
北大核心
1995年第3期167-169,共3页
Journal of Clinical Radiology
关键词
骨肿瘤
巨细胞瘤
青少年
X线诊断
Bone neopalsm Giant cell tumor Children adolescent