肾脏原始神经外胚叶肿瘤1例报告及文献复习  

Peripheral primitive neuroectodermal tumor:A case report and literature reiew

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作  者:宋晶莹[1] 杨江辉[1] 周会芹[1] 鄂盈[1] 李宁[1] 余琦[1] 

机构地区:[1]解放军第309医院病理科,北京100091

出  处:《现代肿瘤医学》2010年第9期1771-1773,共3页Journal of Modern Oncology

摘  要:目的:探讨肾脏外周原始神经外胚叶肿瘤(pPNET)的临床和病理特征。方法:对1例肾脏原始神经外胚叶肿瘤临床表现、病理特征及免疫组化表型进行观察并文献复习。结果:患者男性,35岁,以肉眼血尿为首发症状,B超示左肾上极实性肿物。镜下可见核分裂相,肿瘤坏死明显,免疫组化CD99(+++)、NSE(+)、EMA(-),病变符合原始神经外胚叶肿瘤。结论:原始神经外胚叶肿瘤的诊断依赖病理特征及免疫表型,并需与其他小细胞恶性肿瘤进行鉴别。Objective:To explore the pathological and clinical characteristics of peripheral primitive neuroectoder mal tumor(PNET) of kidney.Methods:A case of PNETs of kidney was reported and the related literatures were reviewed,including the clinical symptoms,pathological characteristics,treatment and survial.Results:One case aged 35 male,the leader symptom was the grass hematuria,pole of left kidney mass,scope below,it was evident that nuclear disord aspect neoplasm necrosis;Tumor necrosis was obvious.Immunohisochemistry:CD99(+++),NSE(+),EMA(-),Pathological changes was PNET.Conclusion: The diagnose of PNET depends on pathological characteristics and expression of immunohisochemistry.

关 键 词:原始神经外胚叶肿瘤 肾脏 免疫组织化学 

分 类 号:R737.11[医药卫生—肿瘤]

 

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