Bertoni F, Unni K K, Beabout J W, Harner S G, Dahlin D C
Am J Clin Pathol. 1987 Jul;88(1):1-9. doi: 10.1093/ajcp/88.1.1.
A series of 30 chondroblastomas was reviewed: 21 had occurred in the lateral part of the temporal bone, 6 in the mandible, 1 in the parietal bone, and 2 in the region that included the temporal bone and mandible. Of the 30 patients in the series, 20 were males and 9 were females; the sex of 1 patient was not stated. The ages of 29 patients ranged from 2 years 11 months to 70 years (mean, 43.5 years). Radiologic findings were not suggestive of a specific diagnosis, although the lesions appeared to be benign. Histologically, most tumors were classic chondroblastomas. However, some showed aneurysmal bone cyst-like areas and nodules of epithelioid cells without chondroid differentiation. Conservative reexcisions were usually curative. Approximately half of the patients had recurrence after curettage.
回顾了一系列30例软骨母细胞瘤：21例发生在颞骨外侧部分，6例发生在下颌骨，1例发生在顶骨，2例发生在包括颞骨和下颌骨的区域。该系列30例患者中，男性20例，女性9例；1例患者的性别未说明。29例患者的年龄范围为2岁11个月至70岁（平均43.5岁）。放射学表现未提示特定诊断，尽管病变似乎是良性的。组织学上，大多数肿瘤为典型软骨母细胞瘤。然而，一些肿瘤显示出动脉瘤样骨囊肿样区域和无软骨样分化的上皮样细胞结节。保守性再次切除通常可治愈。约一半的患者在刮除术后复发。
