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<Article>
<Journal>
				<PublisherName>Cardiovascular research institute, Isfahan University of Medical Sciences</PublisherName>
				<JournalTitle>ARYA Atherosclerosis Journal</JournalTitle>
				<Issn>1735-3955</Issn>
				<Volume>19</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2023</Year>
					<Month>01</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Management of Patients with Vascular Ehlers-Danlos Syndrome and Acute Coronary Syndrome: a Case Report</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>61</FirstPage>
			<LastPage>64</LastPage>
			<ELocationID EIdType="pii">30973</ELocationID>
			
<ELocationID EIdType="doi">10.48305/arya.2022.11722.2343</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Ilenia</FirstName>
					<LastName>Di Liberto</LastName>
<Affiliation>Department of Interventional Cardiology, San Giovanni Di Dio Hospital, Agrigento, Italy</Affiliation>
<Identifier Source="ORCID">0000-0002-1456-8962</Identifier>

</Author>
<Author>
					<FirstName>Gerlando</FirstName>
					<LastName>Pilato</LastName>
<Affiliation>Department of Interventional Cardiology, San Giovanni Di Dio Hospital, Agrigento, Italy</Affiliation>

</Author>
<Author>
					<FirstName>Giuseppe</FirstName>
					<LastName>Caramanno</LastName>
<Affiliation>Department of Interventional Cardiology, San Giovanni Di Dio Hospital, Agrigento, Italy</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2020</Year>
					<Month>12</Month>
					<Day>23</Day>
				</PubDate>
			</History>
		<Abstract>Background: Ehlers-Danlos syndrome (EDS) is a hereditary collagen vascular disorder characterized by joint hypermobility, skin hyperextensibility, and tissue fragility. Vascular EDS (vEDS) is a subtype of EDS which is characterized by vascular fragility.&lt;br /&gt;Case presentation: This is a case report of a young man with vEDS hospitalized for myocardial infarction. He was presented with a coronary dissection and developed aortic dissection, coronary rupture, and cardiac tamponade until death. &lt;br /&gt;Conclusion: This case report highlights how patients with vEDS and acute coronary syndrome show a higher risk of vascular complications compared with other patients, and their admission to the institution with a cardiac surgery room could be helpful and safe for better management of the complications. Non-invasive methods could be useful to exclude other vascular diseases, before the emergency coronary intervention.</Abstract>
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			<Object Type="keyword">
			<Param Name="value">Vascular Ehlers-Danlos syndrome</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Acute Coronary Syndrome</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Coronary dissection</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Aortic Dissection</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Coronary rupture</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Cardiac Tamponade</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://arya.mui.ac.ir/article_30973_c9c824652337e9217278c040b326e9a9.pdf</ArchiveCopySource>
</Article>
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