﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Nickan Research Institute</PublisherName>
      <JournalTitle>Journal of Renal Injury Prevention</JournalTitle>
      <Issn>2345-2781</Issn>
      <Volume>7</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2018</Year>
        <Month>06</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>De novo minimal change disease after kidney transplantation</ArticleTitle>
    <FirstPage>103</FirstPage>
    <LastPage>106</LastPage>
    <ELocationID EIdType="doi">10.15171/jrip.2018.24</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Amirhesam</FirstName>
        <LastName>Alirezaei</LastName>
      </Author>
      <Author>
        <FirstName>Elham</FirstName>
        <LastName>Zare</LastName>
      </Author>
      <Author>
        <FirstName>Mahmoud</FirstName>
        <LastName>Parvin</LastName>
      </Author>
      <Author>
        <FirstName>Fatemeh</FirstName>
        <LastName>Nili</LastName>
      </Author>
      <Author>
        <FirstName>Mahmood</FirstName>
        <LastName>Bakhtiyari</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.15171/jrip.2018.24</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2017</Year>
        <Month>04</Month>
        <Day>03</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2017</Year>
        <Month>08</Month>
        <Day>10</Day>
      </PubDate>
    </History>
    <Abstract>Post-transplant glomerular diseases (PTGN) have been documented frequently, although majority of them, are recurrences of primary diseases. In some cases, de novo glomerular diseases can develop in recipients. In this paper, a case of de novo minimal change disease (MCD) after non-related live donor kidney transplantation in a patient with a history of biopsy proven membranous nephropathy is described. A 25-year-old man with history of biopsy-proven idiopathic membranous glomerulopathy (MGN) who had been transplanted 3 weeks before referred to hospital, presented with peripheral edema and massive proteinuria. First kidney biopsy was compatible with acute cellular rejection with glomerulitis. The patient was treated with methylprednisolone. Panel reactive antibody (PRA) and C4d were negative. Anti- phospholipase A2 receptor (PLA2R) antibody was also negative. Another allograft biopsy was conducted and the result was highly suggestive of MCD. Thus final diagnosis was de novo MCD and proteinuria decreased successfully.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Post-transplant glomerular diseases</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Glomerulitis</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Allograft biopsy</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Minimal change disease</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Anti- phospholipase A2 receptor</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Membranous glomerulopathy</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>