﻿<?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>22</Volume>
      <Issue>9</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2019</Year>
        <Month>09</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Pure Androgen-Secreting Adrenocortical Carcinoma Presenting with Hypoglycemia</ArticleTitle>
    <FirstPage>527</FirstPage>
    <LastPage>530</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Fariba</FirstName>
        <LastName>Karimi</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-6107-4826</Identifier>
      </Author>
      <Author>
        <FirstName>Amirreza</FirstName>
        <LastName>Dehghanian</LastName>
      </Author>
      <Author>
        <FirstName>Mohammadjavad</FirstName>
        <LastName>Fallahi</LastName>
      </Author>
      <Author>
        <FirstName>Behnam</FirstName>
        <LastName>Dalfardi</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">
      </ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2018</Year>
        <Month>12</Month>
        <Day>23</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2019</Year>
        <Month>02</Month>
        <Day>04</Day>
      </PubDate>
    </History>
    <Abstract>Adrenocortical carcinoma (ACC) is a rare and aggressive malignancy. Most patients present with steroid hormone excess or abdominal mass effect. Pure androgen-secreting ACCs are rare, while hypoglycemia is an unusual presentation of this malignancy. We present a 26-year-old woman with hypoglycemia and history of adrenalectomy due to a large adrenal mass which was diagnosed as nonfunctional adrenal adenoma. She was admitted in our hospital 10 days after her fetal loss with repeated episodes of severe hypoglycemia. She had a high serum dehydroepiandrosterone sulfate (DHEA-S) and her hypoglycemia was associated with low insulin and C-peptide levels. Imaging revealed liver metastasis and immunohistochemical studies of the biopsied lesions confirmed the diagnosis of ACC.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Adrenocortical carcinoma</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">C-peptide</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">DHEA-S</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Hypoglycemia</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Insulin</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>