﻿<?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>18</Volume>
      <Issue>6</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2015</Year>
        <Month>06</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Neonatal Testicular Hemangiolymphangioma: A Case Report</ArticleTitle>
    <FirstPage>0</FirstPage>
    <LastPage>0</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Rao</FirstName>
        <LastName>Xu</LastName>
      </Author>
      <Author>
        <FirstName>Tie-Mei</FirstName>
        <LastName>Shi</LastName>
      </Author>
      <Author>
        <FirstName>Shou-Jun</FirstName>
        <LastName>Liu</LastName>
      </Author>
      <Author>
        <FirstName>Xin-Lu</FirstName>
        <LastName>Wang</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">
      </ArticleId>
    </ArticleIdList>
    <History>
    </History>
    <Abstract>A 30-day-old neonate was brought to our hospital due to testicular neoplasm in the right scrotum. Scrotal ultrasonography revealed a mixed cystic and solid mass in the testis. Analysis of testicular tumor markers was negative. Scrotal exploration was performed. A red nodular tumor was removed from the testis by surgery. Histological examination of the specimen showed it to be hemangiolymphangioma (HLA). </Abstract>
  </Article>
</ArticleSet>