﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Tabriz University of Medical Sciences</PublisherName>
      <JournalTitle>Medical Journal of Tabriz University of Medical Sciences</JournalTitle>
      <Issn>2783-2031</Issn>
      <Volume>33</Volume>
      <Issue>4</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2011</Year>
        <Month>10</Month>
        <DAY>25</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>A Case Report of Congenital Pulmonary Airway Malformation in a 20 Weeks Old Fetus</ArticleTitle>
    <FirstPage>95</FirstPage>
    <LastPage>97</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>
        </FirstName>
        <LastName>Amir Vahedi</LastName>
      </Author>
      <Author>
        <FirstName>
        </FirstName>
        <LastName>Zahra Fardiazar</LastName>
      </Author>
      <Author>
        <FirstName>
        </FirstName>
        <LastName>Rasool Estakhri</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">
      </ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2011</Year>
        <Month>10</Month>
        <Day>26</Day>
      </PubDate>
    </History>
    <Abstract>Congenital pulmonary airway malformation is a rare hamartomatous lesion of the lung, which is mostly cystic and fatal. This malformation is the most common congenital lesion in the lung. This lesion is congenital; however prenatal ultrasound examination can assist in prenatal diagnosis. Here, we report autopsy of a 20-weeks fetus with congenital pulmonary airway malformation. This report includes macroscopic and microscopic findings as well.</Abstract>
  </Article>
</ArticleSet>