Pulmonary arteriovenous malformations
Pulmonary arteriovenous malformation, a condition most commonly associated with hereditary hemorrhagic telangiectasia, is an abnormal communication between the pulmonary artery and pulmonary vein without an intervening capillary communication. Although asymptomatic in ~ 50% individuals, it can prese...
Gespeichert in:
Veröffentlicht in: | The International Journal of Cardiovascular Imaging 2019-08, Vol.35 (8), p.1421-1428 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1428 |
---|---|
container_issue | 8 |
container_start_page | 1421 |
container_title | The International Journal of Cardiovascular Imaging |
container_volume | 35 |
creator | Tellapuri, Sreeshma Park, Harold S. Kalva, Sanjeeva P. |
description | Pulmonary arteriovenous malformation, a condition most commonly associated with hereditary hemorrhagic telangiectasia, is an abnormal communication between the pulmonary artery and pulmonary vein without an intervening capillary communication. Although asymptomatic in ~ 50% individuals, it can present with the dreaded complications of stroke or intracranial abscess in high-risk individuals including pregnant women, if untreated. The mainstay of treatment is now endovascular embolization of the feeding artery which can alleviate the symptoms and prevent these complications. In this review, we describe the pathophysiology, methods of screening, diagnostic workup and treatment of these vascular lesions with a particular focus on the currently used embolization techniques and their outcomes. |
doi_str_mv | 10.1007/s10554-018-1479-x |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2129531529</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2129531529</sourcerecordid><originalsourceid>FETCH-LOGICAL-c372t-32c405e795785238ea3bb4dc1963655e665644ff9f294a2d8a368fd8ce8e5a623</originalsourceid><addsrcrecordid>eNp1kMtKAzEUhoMotlYfwI0URHATzf2ylOINCrrQdUhnEpkyM6nJjNS3N8NUBcFVDuQ7_znnA-AUoyuMkLxOGHHOIMIKYiY13O6BKeaSQiQZ3R9qoSGXmk3AUUprhBBBhB6CCUVUCc3lFFw893UTWhs_5zZ2Llbhw7WhT_PG1j7ExnZVaNMxOPC2Tu5k987A693ty-IBLp_uHxc3S1hQSTpIScEQdzInK06ocpauVqwssBZUcO6E4IIx77UnmllSKkuF8qUqnHLcCkJn4HLM3cTw3rvUmaZKhatr27q8lCGYaE4xJzqj53_Qdehjm7cbKKkYo1hlCo9UEUNK0XmziVWTrzUYmcGhGR2a7NAMDs0295ztkvtV48qfjm9pGSAjkPJX--bi7-j_U78Awk57Ag</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2127844318</pqid></control><display><type>article</type><title>Pulmonary arteriovenous malformations</title><source>SpringerLink Journals</source><creator>Tellapuri, Sreeshma ; Park, Harold S. ; Kalva, Sanjeeva P.</creator><creatorcontrib>Tellapuri, Sreeshma ; Park, Harold S. ; Kalva, Sanjeeva P.</creatorcontrib><description>Pulmonary arteriovenous malformation, a condition most commonly associated with hereditary hemorrhagic telangiectasia, is an abnormal communication between the pulmonary artery and pulmonary vein without an intervening capillary communication. Although asymptomatic in ~ 50% individuals, it can present with the dreaded complications of stroke or intracranial abscess in high-risk individuals including pregnant women, if untreated. The mainstay of treatment is now endovascular embolization of the feeding artery which can alleviate the symptoms and prevent these complications. In this review, we describe the pathophysiology, methods of screening, diagnostic workup and treatment of these vascular lesions with a particular focus on the currently used embolization techniques and their outcomes.</description><identifier>ISSN: 1569-5794</identifier><identifier>EISSN: 1573-0743</identifier><identifier>EISSN: 1875-8312</identifier><identifier>DOI: 10.1007/s10554-018-1479-x</identifier><identifier>PMID: 30386957</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Cardiac Imaging ; Cardiology ; Cardiovascular system ; Complications ; Diagnostic systems ; Embolization ; Hemorrhage ; Hereditary hemorrhagic telangiectasia ; Imaging ; Lesions ; Medicine ; Medicine & Public Health ; Pregnancy ; Pulmonary arteries ; Pulmonary artery ; Radiology ; Review Paper</subject><ispartof>The International Journal of Cardiovascular Imaging, 2019-08, Vol.35 (8), p.1421-1428</ispartof><rights>Springer Nature B.V. 2018</rights><rights>The International Journal of Cardiovascular Imaging is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-32c405e795785238ea3bb4dc1963655e665644ff9f294a2d8a368fd8ce8e5a623</citedby><cites>FETCH-LOGICAL-c372t-32c405e795785238ea3bb4dc1963655e665644ff9f294a2d8a368fd8ce8e5a623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10554-018-1479-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10554-018-1479-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30386957$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tellapuri, Sreeshma</creatorcontrib><creatorcontrib>Park, Harold S.</creatorcontrib><creatorcontrib>Kalva, Sanjeeva P.</creatorcontrib><title>Pulmonary arteriovenous malformations</title><title>The International Journal of Cardiovascular Imaging</title><addtitle>Int J Cardiovasc Imaging</addtitle><addtitle>Int J Cardiovasc Imaging</addtitle><description>Pulmonary arteriovenous malformation, a condition most commonly associated with hereditary hemorrhagic telangiectasia, is an abnormal communication between the pulmonary artery and pulmonary vein without an intervening capillary communication. Although asymptomatic in ~ 50% individuals, it can present with the dreaded complications of stroke or intracranial abscess in high-risk individuals including pregnant women, if untreated. The mainstay of treatment is now endovascular embolization of the feeding artery which can alleviate the symptoms and prevent these complications. In this review, we describe the pathophysiology, methods of screening, diagnostic workup and treatment of these vascular lesions with a particular focus on the currently used embolization techniques and their outcomes.</description><subject>Cardiac Imaging</subject><subject>Cardiology</subject><subject>Cardiovascular system</subject><subject>Complications</subject><subject>Diagnostic systems</subject><subject>Embolization</subject><subject>Hemorrhage</subject><subject>Hereditary hemorrhagic telangiectasia</subject><subject>Imaging</subject><subject>Lesions</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Pregnancy</subject><subject>Pulmonary arteries</subject><subject>Pulmonary artery</subject><subject>Radiology</subject><subject>Review Paper</subject><issn>1569-5794</issn><issn>1573-0743</issn><issn>1875-8312</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp1kMtKAzEUhoMotlYfwI0URHATzf2ylOINCrrQdUhnEpkyM6nJjNS3N8NUBcFVDuQ7_znnA-AUoyuMkLxOGHHOIMIKYiY13O6BKeaSQiQZ3R9qoSGXmk3AUUprhBBBhB6CCUVUCc3lFFw893UTWhs_5zZ2Llbhw7WhT_PG1j7ExnZVaNMxOPC2Tu5k987A693ty-IBLp_uHxc3S1hQSTpIScEQdzInK06ocpauVqwssBZUcO6E4IIx77UnmllSKkuF8qUqnHLcCkJn4HLM3cTw3rvUmaZKhatr27q8lCGYaE4xJzqj53_Qdehjm7cbKKkYo1hlCo9UEUNK0XmziVWTrzUYmcGhGR2a7NAMDs0295ztkvtV48qfjm9pGSAjkPJX--bi7-j_U78Awk57Ag</recordid><startdate>20190801</startdate><enddate>20190801</enddate><creator>Tellapuri, Sreeshma</creator><creator>Park, Harold S.</creator><creator>Kalva, Sanjeeva P.</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M7Z</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20190801</creationdate><title>Pulmonary arteriovenous malformations</title><author>Tellapuri, Sreeshma ; Park, Harold S. ; Kalva, Sanjeeva P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-32c405e795785238ea3bb4dc1963655e665644ff9f294a2d8a368fd8ce8e5a623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Cardiac Imaging</topic><topic>Cardiology</topic><topic>Cardiovascular system</topic><topic>Complications</topic><topic>Diagnostic systems</topic><topic>Embolization</topic><topic>Hemorrhage</topic><topic>Hereditary hemorrhagic telangiectasia</topic><topic>Imaging</topic><topic>Lesions</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Pregnancy</topic><topic>Pulmonary arteries</topic><topic>Pulmonary artery</topic><topic>Radiology</topic><topic>Review Paper</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tellapuri, Sreeshma</creatorcontrib><creatorcontrib>Park, Harold S.</creatorcontrib><creatorcontrib>Kalva, Sanjeeva P.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>The International Journal of Cardiovascular Imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tellapuri, Sreeshma</au><au>Park, Harold S.</au><au>Kalva, Sanjeeva P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pulmonary arteriovenous malformations</atitle><jtitle>The International Journal of Cardiovascular Imaging</jtitle><stitle>Int J Cardiovasc Imaging</stitle><addtitle>Int J Cardiovasc Imaging</addtitle><date>2019-08-01</date><risdate>2019</risdate><volume>35</volume><issue>8</issue><spage>1421</spage><epage>1428</epage><pages>1421-1428</pages><issn>1569-5794</issn><eissn>1573-0743</eissn><eissn>1875-8312</eissn><abstract>Pulmonary arteriovenous malformation, a condition most commonly associated with hereditary hemorrhagic telangiectasia, is an abnormal communication between the pulmonary artery and pulmonary vein without an intervening capillary communication. Although asymptomatic in ~ 50% individuals, it can present with the dreaded complications of stroke or intracranial abscess in high-risk individuals including pregnant women, if untreated. The mainstay of treatment is now endovascular embolization of the feeding artery which can alleviate the symptoms and prevent these complications. In this review, we describe the pathophysiology, methods of screening, diagnostic workup and treatment of these vascular lesions with a particular focus on the currently used embolization techniques and their outcomes.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>30386957</pmid><doi>10.1007/s10554-018-1479-x</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1569-5794 |
ispartof | The International Journal of Cardiovascular Imaging, 2019-08, Vol.35 (8), p.1421-1428 |
issn | 1569-5794 1573-0743 1875-8312 |
language | eng |
recordid | cdi_proquest_miscellaneous_2129531529 |
source | SpringerLink Journals |
subjects | Cardiac Imaging Cardiology Cardiovascular system Complications Diagnostic systems Embolization Hemorrhage Hereditary hemorrhagic telangiectasia Imaging Lesions Medicine Medicine & Public Health Pregnancy Pulmonary arteries Pulmonary artery Radiology Review Paper |
title | Pulmonary arteriovenous malformations |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T02%3A07%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pulmonary%20arteriovenous%20malformations&rft.jtitle=The%20International%20Journal%20of%20Cardiovascular%20Imaging&rft.au=Tellapuri,%20Sreeshma&rft.date=2019-08-01&rft.volume=35&rft.issue=8&rft.spage=1421&rft.epage=1428&rft.pages=1421-1428&rft.issn=1569-5794&rft.eissn=1573-0743&rft_id=info:doi/10.1007/s10554-018-1479-x&rft_dat=%3Cproquest_cross%3E2129531529%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2127844318&rft_id=info:pmid/30386957&rfr_iscdi=true |