Anderson W J, Bowers W H
J Hand Surg Br. 1986 Feb;11(1):144-6. doi: 10.1016/0266-7681(86)90040-9.
Chondromyxoid fibroma is a rare benign tumour of chondral origin. The diagnosis is difficult, but as Jaffe emphasized, "its recognition is of some importance in that pathologically it may be mistaken for sarcoma and, as such, treated more radically than is necessary" (Jaffe, 1948). Salzer (1965) found only 136 cases in the world literature since 1948 when Jaffe defined the criteria for their histological diagnosis. Only six cases of chondromyxoid fibroma have been reported involving the hand (Frank, Rockwood, 1969; Zatyepin, Klimova, Lipkin, Perety, 1979).
软骨黏液样纤维瘤是一种罕见的起源于软骨的良性肿瘤。诊断较为困难,但正如贾菲所强调的,“认识到它很重要,因为在病理上它可能被误诊为肉瘤,从而接受比必要程度更激进的治疗”(贾菲,1948年)。自1948年贾菲确定其组织学诊断标准以来,萨尔泽(1965年)在世界文献中仅发现136例。仅有6例手部软骨黏液样纤维瘤的病例报告(弗兰克、罗克伍德,1969年;扎捷平、克利莫娃、利普金、佩列蒂,1979年)。