Bouaziz Mouna Chelli, Chaabane Skander, Mrad Karima, Oueslati Seddik, Bellassoued Anis, Ladeb Mohamed F, Rhomdhane Khaled Ben
Service de radiologie, Institut MT Kassab, Ksar Said, Tunis-Tunisia.
J Comput Assist Tomogr. 2005 Mar-Apr;29(2):254-9. doi: 10.1097/01.rct.0000159581.54555.08.
Primary leiomyosarcoma of bone is a very rare tumor. Four cases are reported: 3 tumors were located in the femur and 1 in the talus. Clinical and imaging findings including radiographs, CT, and MRI are described. The final diagnosis was made by histopathological, immunohistochemical, and/or ultrastructural study after biopsy.
原发性骨平滑肌肉瘤是一种非常罕见的肿瘤。本文报告4例:3例肿瘤位于股骨,1例位于距骨。描述了包括X线片、CT和MRI在内的临床及影像学表现。活检后通过组织病理学、免疫组织化学和/或超微结构研究做出最终诊断。