Abramovici Luigia, Kenan Samuel, Hytiroglou Prodromos, Rafii Mahvash, Steiner German C
Department of Pathology and Laboratory Medicine, Hospital for Joint Diseases, 301 E. 17 Street, New York, NY 10003, USA.
Skeletal Radiol. 2002 Mar;31(3):179-82. doi: 10.1007/s00256-001-0458-8. Epub 2002 Jan 23.
We report a case of a 14-year-old boy with an intracompartmental lytic lesion with poorly defined margins in the right distal tibia that was originally treated with curettage and bone grafting. Histologic examination showed an osteoblastic tumor with unusual features, which was found on consultation to be an osteoblastoma-like osteosarcoma, a rare, low-grade variant of osteosarcoma. Subsequently, the patient underwent en bloc resection of the distal tibia, which was replaced with vascularized bone graft and followed by chemotherapy. Two years later, he is alive with lung metastases.
我们报告一例14岁男孩,其右胫骨远端存在一个骨内溶骨性病变,边界不清,最初接受了刮除术和骨移植治疗。组织学检查显示为具有不寻常特征的成骨细胞瘤,经会诊发现是成骨细胞瘤样骨肉瘤,这是骨肉瘤的一种罕见的低级别变体。随后,患者接受了胫骨远端整块切除术,并用带血管蒂骨移植进行替代,随后进行化疗。两年后,他存活但有肺转移。