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<ArticleSet>
<Article>
<Journal>
				<PublisherName>Iranian Heart Association</PublisherName>
				<JournalTitle>Iranian Heart Journal</JournalTitle>
				<Issn></Issn>
				<Volume>9</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2008</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Congenital Coronary Artery Fistulas: Report of Three Rare Cases</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>64</FirstPage>
			<LastPage>68</LastPage>
			<ELocationID EIdType="pii">182396</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2007</Year>
					<Month>07</Month>
					<Day>22</Day>
				</PubDate>
			</History>
		<Abstract>Coronary artery fistula is a rare congenital anomaly with an incidence of about 0.2 - 0.6% in&lt;br /&gt;different reports. It is defined as a direct communication between the coronary artery and any&lt;br /&gt;surrounding cardiac chamber or vascular structure which bypasses the myocardial capillary bed.&lt;br /&gt;Three interesting cases of coronary artery fistula are reported. Two of the patients were&lt;br /&gt;symptomatic. In one case, all coronary arteries (in addition to duplicated LAD) were fistulized into&lt;br /&gt;the right ventricle. Diagnosis was made by echocardiographic study and coronary angiography.&lt;br /&gt;Surgical correction is discussed. In one case, angiography six months later showed no fistula. Serial&lt;br /&gt;echocardiography during follow-up was unremarkable (Iranian Heart Journal 2008; 9 (1):64 -68).</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">coronary artery fistula■ congenital heart disease</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://journal.iha.org.ir/article_182396_10dae2db89bc660a12ae0a03ec03a28d.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
