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塌陷性肾小球病 2

来源:医学杂志 2006-08-16 20:14:03 

WT1和Pax-2蛋白。正常生理情况下,WT1蛋白存在于肾单位形成期及成年肾脏的足突细胞核中,Pax-2仅在肾小囊上皮细胞核中。CG患者足突细胞核内WT1减少,而胞浆中增多,少数病人肾小球上皮细胞核中有异常的Pax2表达。Meyrier等人[10]则提出在CG中足突细胞与肾小球基底膜分离,脱落至包曼氏囊腔,积聚在肾小管腔内,转变成巨噬细胞样细胞,与严重的小管间质病变相关。有学者发现1例α-干扰素治疗的丙型肝炎患者发生CG,停药后重新肾活检证实肾脏病变恢复为FSGS[11]。还有人在CG患者标本中用PCR方法检测到细小病毒B19(PV19)较FSGS多[12]。上述研究结果显示CG肾活检发病机理已引起广泛重视,但要明确阐述其发病机理,尚需更多更深入的研究。

  综上所述,塌陷性肾小球病是新的病理概念,有独特的病理特点,预后差,它已经为越来越多的肾脏病理学家所重视。

  作者单位:100034 北京医科大学第一医院肾内科

参考文献

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  10 Bariety J,Nochy D,Mandet C,et al.Podocytes undergo phenotypic changes and express macrophagic-associated markers in idiopathic callapsing glomerulopathy.Kidney Int,1998,53:918-925.

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