Kransdorf M J, Smith S E
Department of Radiology, Mayo Clinic, Jacksonville, Florida, USA.
Semin Musculoskelet Radiol. 2000;4(1):113-25. doi: 10.1055/s-2000-6859.
Langerhans cell histiocytosis (LCH) and Ewing sarcoma represent lesions of unknown histogenesis. Both lesions typically affect children and adolescents. Imaging features frequently suggest the diagnosis, and both lesions may demonstrate aggressive characteristics. LCH shows a broader spectrum of imaging findings, depending on lesion activity and location, which are reviewed in this article. Ewing sarcoma typically reveals both osseous and soft tissue involvement, although direct continuity of the components is often not apparent. Knowledge of the spectrum of clinical and radiologic features facilitates early diagnosis and can be used to evaluate the effects of therapy.
朗格汉斯细胞组织细胞增多症(LCH)和尤因肉瘤代表组织发生不明的病变。这两种病变通常影响儿童和青少年。影像学特征常常提示诊断,且两种病变都可能表现出侵袭性特征。LCH根据病变的活动度和位置显示出更广泛的影像学表现,本文将对此进行综述。尤因肉瘤通常显示骨和软组织均受累,尽管各组成部分之间的直接连续性往往不明显。了解临床和放射学特征谱有助于早期诊断,并可用于评估治疗效果。