Kosaki N, Yabe H, Anazawa U, Morioka H, Mukai M, Toyama Y
Department of Orthopaedic Surgery, Keio University School of Medicine, Tokyo, Japan.
Skeletal Radiol. 2005 Aug;34(8):477-84. doi: 10.1007/s00256-004-0889-0. Epub 2005 Feb 19.
We treated a 26-year-old man with a 19-year history of Ollier's disease. Secondary chondrosarcomas developed metachronously at four separate locations: both femora, left proximal tibia and fibular head. All four lesions were surgically excised, and each specimen was histologically identified as grade 1 or 2 chondrosarcoma. Clinical follow-up for 20 years beginning at the time of first tumor surgery has shown no evidence of local recurrence or metastasis. This is the first report of multiple bilateral metachronous malignant transformation of multiple chondromatoses in a patient with Ollier's disease.
我们治疗了一名患有19年Ollier病病史的26岁男性。继发性软骨肉瘤在四个不同部位同步发生:双侧股骨、左胫骨近端和腓骨头。所有四个病灶均通过手术切除,每个标本经组织学鉴定为1级或2级软骨肉瘤。从首次肿瘤手术时开始的20年临床随访显示,没有局部复发或转移的迹象。这是首例关于Ollier病患者多处软骨瘤病发生多部位双侧同步恶性转化的报告。