﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Academy of Medical Sciences of I.R. Iran</PublisherName>
      <JournalTitle>Archives of Iranian Medicine</JournalTitle>
      <Issn>1029-2977</Issn>
      <Volume>16</Volume>
      <Issue>8</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2013</Year>
        <Month>08</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Visceral Leishmaniasis-associated Hemophagocytosis: A Single Center Experience</ArticleTitle>
    <FirstPage>0</FirstPage>
    <LastPage>0</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Maral</FirstName>
        <LastName>Mokhtari</LastName>
      </Author>
      <Author>
        <FirstName>Perikala</FirstName>
        <LastName>Vijayananda Kumar</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">
      </ArticleId>
    </ArticleIdList>
    <History>
    </History>
    <Abstract>BACKGROUND: Kala-azar is a multisystem infection of the reticuloendothelial system. Various hematologic abnormalities have been described in kala-azar including hemophagocytic syndrome (HPS). METHODS: We reviewed bone marrow aspirate smears from 18 documented cases of kala-azar complicated by HPS. RESULTS: The bone marrow smears were hypercellular with erythroid hyperplasia. Megaloblastic changes, foamy macrophages, activated macrophages with cytoplasmic vacuoles and elongated cytoplasmic process, intra- and extracellular amastigotes, cytoplasmic fragments (blue bodies), plasma cells with inclusions and hemophagocytic cells were seen. Leishman bodies (amastigotes) were also found in some hemophagocytic cells. CONCLUSION: Kala-azar should be considered as an etiology of HPS, particularly in endemic areas.</Abstract>
  </Article>
</ArticleSet>