Sirikulchayanonta Vorachai, Jaovisidh Suphaneewan
Department of Pathology, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
J Med Assoc Thai. 2008 Feb;91(2):244-8.
The authors present a case of a 42-year-old female who developed a leiomyosarcoma of the right proximal tibia that appeared radiologically similar to a giant cell tumor Histology revealed spindle cells running in whorl-like fashion with focal atypia and low mitotic figures. The immuno-stains revealed positive reactivity for alpha-smooth muscle (SMA), muscle actin and cytokeratin (AE1/AE3). The authors rendered a diagnosis of low-grade leiomyosarcoma of bone. The lesion was considered a primary lesion since the patient did not have other leiomyomatous tumors. The MRI showed hypo- to iso- signal intensity on T1-weighted imaging and heterogeneous intensity on T2-weighted imaging. This was likely due to admixed fibrotic tissue in the lesion. The tumor cells were not positive for Ebstein-Barr virus by in-situ hybridization as seen in leiomyomatous tumors in immunodeficiency patients.
作者报告了一例42岁女性,其右胫骨近端发生平滑肌肉瘤,影像学表现与骨巨细胞瘤相似。组织学检查显示梭形细胞呈漩涡状排列,有局灶性异型性和低核分裂象。免疫组化染色显示α-平滑肌肌动蛋白(SMA)、肌动蛋白和细胞角蛋白(AE1/AE3)呈阳性反应。作者诊断为骨低度恶性平滑肌肉瘤。由于患者没有其他平滑肌瘤性肿瘤,该病变被认为是原发性病变。MRI显示在T1加权像上呈低至等信号强度,在T2加权像上呈不均匀信号强度。这可能是由于病变中混有纤维化组织。原位杂交显示肿瘤细胞不像免疫缺陷患者的平滑肌瘤性肿瘤那样对EB病毒呈阳性反应。