Bahk W J, Mirra J M, Sohn K R, Shin D S
Orthopaedic Oncology, Orthopaedic Hospital, Los Angeles, CA, USA.
Ann Diagn Pathol. 1998 Aug;2(4):241-6. doi: 10.1016/s1092-9134(98)80013-0.
A 19-year-old man presented with a chondromyxoid fibroma of the distal phalanx of the great toe that was originally diagnosed as osteosarcoma rather than "dedifferentiated" chondrosarcoma. Radiographs showed a large, expansive, and calcified tumor of the distal phalanx. Although the tumor had the architectural and matrix patterns of a chondromyxoid fibroma, high-power examination demonstrated that the lesion had such severe nuclear pleomorphism that it was mistaken for high-grade sarcoma. The purpose of this report is to present the criteria used to differentiate a benign pseudoanaplastic chondromyxoid fibroma from chondrogenic high-grade sarcomas.
一名19岁男性患者,大脚趾远节指骨出现软骨黏液样纤维瘤,最初被诊断为骨肉瘤而非“去分化”软骨肉瘤。X线片显示远节指骨有一个大的、膨胀性且钙化的肿瘤。尽管该肿瘤具有软骨黏液样纤维瘤的结构和基质模式,但高倍镜检查显示病变具有如此严重的核多形性,以至于被误诊为高级别肉瘤。本报告的目的是介绍用于区分良性假间变性软骨黏液样纤维瘤与软骨源性高级别肉瘤的标准。