Takami K M, Ishida T, Ieguchi M, Kuniyoshi Y, Wakasa K, Sakurai M
Department of Orthopaedic Surgery, Osaka City University Medical School, Japan.
Int Orthop. 1994;18(4):248-51. doi: 10.1007/BF00188330.
We report a case of what appeared to be a primary leiomyosarcoma of the left pubic bone of a female aged 23 years. Forty-eight cases of the tumour have been recorded in the literature since 1944, only two of which were in the pelvis. The tumour in our patient was treated by curettage and there was no recurrence in the following 3 years. The tumour cells showed only mild cellular atypism and 2 to 3 mitoses per 10 high-power fields. These finding suggest that the tumour might be an extremely rare leiomyoma of bone.
我们报告一例23岁女性左耻骨原发性平滑肌肉瘤病例。自1944年以来，文献中已记录了48例该肿瘤病例，其中仅有两例位于骨盆。我们的患者接受了刮除术治疗，在随后的3年中未复发。肿瘤细胞仅表现出轻度细胞异型性，每10个高倍视野有2至3个有丝分裂象。这些发现提示该肿瘤可能是一种极为罕见的骨平滑肌瘤。
