Giant right atrial aneurysm with atrial fibrillation
Congenital right atrial aneurysm is a rare condition. Here we reported a 16‐year‐old male with giant right atrial aneurysm, atrial fibrillation, and atrial septal defect. Surgical resection of extensive right atrium, ASD repair, and maze procedure were performed. In the present case, we found extens...
Gespeichert in:
Veröffentlicht in: | Journal of cardiac surgery 2019-12, Vol.34 (12), p.1647-1648 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1648 |
---|---|
container_issue | 12 |
container_start_page | 1647 |
container_title | Journal of cardiac surgery |
container_volume | 34 |
creator | Qin, Chaoyi Yan, Yangbo Gan, Changping |
description | Congenital right atrial aneurysm is a rare condition. Here we reported a 16‐year‐old male with giant right atrial aneurysm, atrial fibrillation, and atrial septal defect. Surgical resection of extensive right atrium, ASD repair, and maze procedure were performed. In the present case, we found extensive enlargement of right atrium protruding to the apex on the surface of the right ventricle. With the exist of atrial fibrillation, thrombus formation was always a lethal threat. Surgical treatment can provide excellent clinical results and further avoided life‐threatening complications. |
doi_str_mv | 10.1111/jocs.14335 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2313356446</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2313356446</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3655-657b5162d8f33e428e2473bb1e4518f6bc7942360aef4a83dfa7919608859a673</originalsourceid><addsrcrecordid>eNp9kE1LAzEQhoMotlYv_gDZowirmXxt9ihFq1LoQT2H7DaxKftRk11K_72p23p0LgPDw8s7D0LXgO8hzsO6LcM9MEr5CRoDZziVkMMpGmMpRYoZwyN0EcIaY0IYxedoRCHDPEJjxGZON13i3deqS3Tnna4S3Zje70KdbF23Oh6tK7yrKt25trlEZ1ZXwVwd9gR9Pj99TF_S-WL2On2cpyUVnKeCZwUHQZbSUmoYkYawjBYFGMZBWlGUWc4IFVgby7SkS6uzHHIRa_Nci4xO0O2Qu_Htd29Cp2oXShNbNKbtgyIU4tOCMRHRuwEtfRuCN1ZtvKu13ynAam9J7S2pX0sRvjnk9kVtln_oUUsEYAC2rjK7f6LU22L6PoT-AMBxcHg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2313356446</pqid></control><display><type>article</type><title>Giant right atrial aneurysm with atrial fibrillation</title><source>Wiley Online Library</source><creator>Qin, Chaoyi ; Yan, Yangbo ; Gan, Changping</creator><creatorcontrib>Qin, Chaoyi ; Yan, Yangbo ; Gan, Changping</creatorcontrib><description>Congenital right atrial aneurysm is a rare condition. Here we reported a 16‐year‐old male with giant right atrial aneurysm, atrial fibrillation, and atrial septal defect. Surgical resection of extensive right atrium, ASD repair, and maze procedure were performed. In the present case, we found extensive enlargement of right atrium protruding to the apex on the surface of the right ventricle. With the exist of atrial fibrillation, thrombus formation was always a lethal threat. Surgical treatment can provide excellent clinical results and further avoided life‐threatening complications.</description><identifier>ISSN: 0886-0440</identifier><identifier>EISSN: 1540-8191</identifier><identifier>DOI: 10.1111/jocs.14335</identifier><identifier>PMID: 31705819</identifier><language>eng</language><publisher>United States</publisher><subject>atrial aneurysm ; atrial fibrillation ; congenital heart disease</subject><ispartof>Journal of cardiac surgery, 2019-12, Vol.34 (12), p.1647-1648</ispartof><rights>2019 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3655-657b5162d8f33e428e2473bb1e4518f6bc7942360aef4a83dfa7919608859a673</citedby><cites>FETCH-LOGICAL-c3655-657b5162d8f33e428e2473bb1e4518f6bc7942360aef4a83dfa7919608859a673</cites><orcidid>0000-0001-7340-0628 ; 0000-0002-7092-161X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjocs.14335$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjocs.14335$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31705819$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qin, Chaoyi</creatorcontrib><creatorcontrib>Yan, Yangbo</creatorcontrib><creatorcontrib>Gan, Changping</creatorcontrib><title>Giant right atrial aneurysm with atrial fibrillation</title><title>Journal of cardiac surgery</title><addtitle>J Card Surg</addtitle><description>Congenital right atrial aneurysm is a rare condition. Here we reported a 16‐year‐old male with giant right atrial aneurysm, atrial fibrillation, and atrial septal defect. Surgical resection of extensive right atrium, ASD repair, and maze procedure were performed. In the present case, we found extensive enlargement of right atrium protruding to the apex on the surface of the right ventricle. With the exist of atrial fibrillation, thrombus formation was always a lethal threat. Surgical treatment can provide excellent clinical results and further avoided life‐threatening complications.</description><subject>atrial aneurysm</subject><subject>atrial fibrillation</subject><subject>congenital heart disease</subject><issn>0886-0440</issn><issn>1540-8191</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhoMotlYv_gDZowirmXxt9ihFq1LoQT2H7DaxKftRk11K_72p23p0LgPDw8s7D0LXgO8hzsO6LcM9MEr5CRoDZziVkMMpGmMpRYoZwyN0EcIaY0IYxedoRCHDPEJjxGZON13i3deqS3Tnna4S3Zje70KdbF23Oh6tK7yrKt25trlEZ1ZXwVwd9gR9Pj99TF_S-WL2On2cpyUVnKeCZwUHQZbSUmoYkYawjBYFGMZBWlGUWc4IFVgby7SkS6uzHHIRa_Nci4xO0O2Qu_Htd29Cp2oXShNbNKbtgyIU4tOCMRHRuwEtfRuCN1ZtvKu13ynAam9J7S2pX0sRvjnk9kVtln_oUUsEYAC2rjK7f6LU22L6PoT-AMBxcHg</recordid><startdate>201912</startdate><enddate>201912</enddate><creator>Qin, Chaoyi</creator><creator>Yan, Yangbo</creator><creator>Gan, Changping</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7340-0628</orcidid><orcidid>https://orcid.org/0000-0002-7092-161X</orcidid></search><sort><creationdate>201912</creationdate><title>Giant right atrial aneurysm with atrial fibrillation</title><author>Qin, Chaoyi ; Yan, Yangbo ; Gan, Changping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3655-657b5162d8f33e428e2473bb1e4518f6bc7942360aef4a83dfa7919608859a673</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>atrial aneurysm</topic><topic>atrial fibrillation</topic><topic>congenital heart disease</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qin, Chaoyi</creatorcontrib><creatorcontrib>Yan, Yangbo</creatorcontrib><creatorcontrib>Gan, Changping</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cardiac surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qin, Chaoyi</au><au>Yan, Yangbo</au><au>Gan, Changping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Giant right atrial aneurysm with atrial fibrillation</atitle><jtitle>Journal of cardiac surgery</jtitle><addtitle>J Card Surg</addtitle><date>2019-12</date><risdate>2019</risdate><volume>34</volume><issue>12</issue><spage>1647</spage><epage>1648</epage><pages>1647-1648</pages><issn>0886-0440</issn><eissn>1540-8191</eissn><abstract>Congenital right atrial aneurysm is a rare condition. Here we reported a 16‐year‐old male with giant right atrial aneurysm, atrial fibrillation, and atrial septal defect. Surgical resection of extensive right atrium, ASD repair, and maze procedure were performed. In the present case, we found extensive enlargement of right atrium protruding to the apex on the surface of the right ventricle. With the exist of atrial fibrillation, thrombus formation was always a lethal threat. Surgical treatment can provide excellent clinical results and further avoided life‐threatening complications.</abstract><cop>United States</cop><pmid>31705819</pmid><doi>10.1111/jocs.14335</doi><tpages>2</tpages><orcidid>https://orcid.org/0000-0001-7340-0628</orcidid><orcidid>https://orcid.org/0000-0002-7092-161X</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0886-0440 |
ispartof | Journal of cardiac surgery, 2019-12, Vol.34 (12), p.1647-1648 |
issn | 0886-0440 1540-8191 |
language | eng |
recordid | cdi_proquest_miscellaneous_2313356446 |
source | Wiley Online Library |
subjects | atrial aneurysm atrial fibrillation congenital heart disease |
title | Giant right atrial aneurysm with atrial fibrillation |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-25T05%3A49%3A12IST&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=Giant%20right%20atrial%20aneurysm%20with%20atrial%20fibrillation&rft.jtitle=Journal%20of%20cardiac%20surgery&rft.au=Qin,%20Chaoyi&rft.date=2019-12&rft.volume=34&rft.issue=12&rft.spage=1647&rft.epage=1648&rft.pages=1647-1648&rft.issn=0886-0440&rft.eissn=1540-8191&rft_id=info:doi/10.1111/jocs.14335&rft_dat=%3Cproquest_cross%3E2313356446%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=2313356446&rft_id=info:pmid/31705819&rfr_iscdi=true |