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<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Society of Diabetic Nephropathy Prevention</PublisherName>
      <JournalTitle>Journal of Nephropathology</JournalTitle>
      <Issn>2251-8363</Issn>
      <Volume>6</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2017</Year>
        <Month>07</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Self-limited membranous nephropathy after intravitreal bevacizumab therapy for age-related macular degeneration</ArticleTitle>
    <FirstPage>134</FirstPage>
    <LastPage>137</LastPage>
    <ELocationID EIdType="doi">10.15171/jnp.2017.23</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Gebran</FirstName>
        <LastName>Khneizer</LastName>
      </Author>
      <Author>
        <FirstName>Ahmad</FirstName>
        <LastName>Al-Taee</LastName>
      </Author>
      <Author>
        <FirstName>Bahar</FirstName>
        <LastName>Bastani</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.15171/jnp.2017.23</ArticleId>
    </ArticleIdList>
    <History>
    </History>
    <Abstract>Background: Monoclonal antibodies targeting vascular endothelial growth factor (VEGF), such as bevacizumab, are administered intravitreally for the treatment of wet or exudative age-related macular degeneration (ARMD). Systemic use of bevacizumab has been linked to a wide range of renal adverse effects including proteinuria and hypertension. Case Presentation: We present the case of a 77-year-old Caucasian male with a past medical history of hypertension, vitamin D deficiency and paroxysmal atrial fibrillation who presented to primary care clinic with a 2-week history of bilateral lower extremity edema, 2 months after completing four monthly intravitreal injections of bevacizumab for ARMD. Examination was remarkable for blood pressure of 187/91 mm Hg and severe bilateral lower extremity edema. Work up revealed unremarkable complete blood count (CBC), comprehensive metabolic panel (CMP), lipid panel, and echocardiography, except for 491 mg/dL albuminuria. Metoprolol and furosemide were added to hydrochlorothiazide and lisinopril. Work up by nephrology consult team five months later was notable for a urinalysis revealing 3 red blood cells/high power field (RBC/HPF), 24-hour urine protein of 8.6 g, and serum creatinine of 1.2 mg/dL. Viral hepatitis panel, total complement activity (CH50), C3, C4, anti-nuclear antibody (ANA), anti-neutrophil cytoplasmic antibody (ANCA), serum and urine protein electrophoresis were all unremarkable. Renal biopsy was consistent with membranous nephropathy. Age-appropriate cancer screening was negative. Random urine protein-to-creatinine ratio declined to 2 g/g and then to 0.56 g/g at 7 and 10 months follow up, respectively. Serum blood urea nitrogen (BUN) and creatinine remained normal throughout the course of illness and patient did not require any immunosuppressive treatment. Conclusions: The wide range of nephrotoxicity after systemic bevacizumab has been well documented. Our case describes a self-limited biopsy-proven membranous nephropathy after intravitreal bevacizumab injections.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Membranous nephropathy</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Proteinuria</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Nephrotic syndrome</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Age-related Macular degeneration</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Vascular endothelial growth factor</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">VEGF???</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>