﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Nickan Research Institute</PublisherName>
      <JournalTitle>Journal of Renal Endocrinology</JournalTitle>
      <Issn>2423-6438</Issn>
      <Volume>5</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2019</Year>
        <Month>01</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Rosai-Dorfman disease; a case report and review of the literature</ArticleTitle>
    <FirstPage>e10</FirstPage>
    <LastPage>e10</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Shakiba</FirstName>
        <LastName>Hassanzadeh</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-5091-5191</Identifier>
      </Author>
      <Author>
        <FirstName>Parto</FirstName>
        <LastName>Nasri</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-9596-8860</Identifier>
      </Author>
      <Author>
        <FirstName>Mohammadreza</FirstName>
        <LastName>Khosravifarsani</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-4271-7846</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">
      </ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2019</Year>
        <Month>10</Month>
        <Day>16</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>12</Month>
        <Day>02</Day>
      </PubDate>
    </History>
    <Abstract>Rosai-Dorfman disease (RDD) also known as sinus histiocytosis with massive lymphadenopathy (SHML) is a rare idiopathic and benign disorder. We report a case of a previously healthy 44-year-old female patient who first presented with painless enlargement of the submandibular and parotid glands. She, later on, experienced multiple recurrences. The diagnosis of RDD in this patient was confirmed with pathology examinations and immunohistochemistry evaluations. </Abstract>
  </Article>
</ArticleSet>