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作 者:方新颜[1,2] 张智弘[1] 张炜明[1] 范钦和[1] 潘敏鸿[1]
机构地区:[1]南京医科大学第一附属医院病理科,南京210029 [2]江苏省启东市中医院病理科,启东226200
出 处:《中国体视学与图像分析》2014年第3期287-293,共7页Chinese Journal of Stereology and Image Analysis
摘 要:目的探讨脑膜血管周细胞瘤发生颅外转移的临床病理特征、诊断与鉴别诊断要点。方法对9例发生颅外转移的脑膜血管周细胞瘤进行临床病理分析、组织形态学及免疫组化染色观察,结合文献对其,临床表现、病理形态特点及鉴别诊断进行探讨。结果患者年龄32~59岁,男性3例,女性6例。转移部位有肝、肺、骨、腹腔、皮下等。转移间隔时间0.5~10年不等,光镜下瘤细胞为形态大小较一致的短梭形细胞,瘤细胞间富于小血管,呈裂隙状或“鹿角状”,核卵圆形,具有非典型性,核分裂象多少不等,WHOII级或III级。免疫组化瘤细胞波形蛋白均呈强阳性表达,CD34阳性程度不等,弥漫阳性或局灶阳性。结论脑膜血管周细胞瘤临床呈侵袭性,易复发和转移到中枢神经系统外,鉴别诊断包括孤立性纤维性肿瘤、脑膜瘤及间叶性软骨肉瘤等。Objective To investigate the clinicopathological and diagnostic characteristics of meningeal haemangiopericytoma (M-HPC) with extracranial metastasis. Methods The clinical presentation, histo- logical changes and immunohistochemieal staining were analyzed in nine cases of M-HPC with extracranial metastasis and related literatures were reviewed. Results Their ages ranged from 32 to 59 years old, 3 males and 6 females. The neous tissue. The interval included liver, ranges from half sites of metastasis time of metastasis lung, bone, peritoneal cavity, and subcuta- a year to 10 years. Histologically, the tumor was composed of spindle-shaped cells and numerous vascular pattern with a "staghorn configuration". Im- munohistochemicalty, the cells were typically positive for vimentin, and CD34. Conclusions M-HPC is a rare malignant tumor with aggressive behavior and can easily recur or metastasize to extracranial sites Its differential diagnosis includes solitary fibrous tumor, meningioma, and mesenchymal chondrosarcoma
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