Loading…
Contrast enhanced computed tomography findings of persistent truncus arteriosus; A rare congenital heart disease
Persistent Truncus Arteriosus is a cyanotic congenital heart anomaly in which a single trunk supplies both the pulmonary and systemic circulation, instead of a separate aorta and a pulmonary trunk. It is usually classified as a conotruncal anomaly. Due to parallel fetal circulation, truncus arterios...
Saved in:
Published in: | Radiology case reports 2020-06, Vol.15 (6), p.795-798 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c3577-f6c9131582b841eaae57647f116f0f88febeca766db2cf249efacf7db0d773093 |
container_end_page | 798 |
container_issue | 6 |
container_start_page | 795 |
container_title | Radiology case reports |
container_volume | 15 |
creator | Turkoglu, Saim Batur, Abdussamet Yokuş, Adem Dündar, İlyas Akinci, Muhammed Bilal |
description | Persistent Truncus Arteriosus is a cyanotic congenital heart anomaly in which a single trunk supplies both the pulmonary and systemic circulation, instead of a separate aorta and a pulmonary trunk. It is usually classified as a conotruncal anomaly. Due to parallel fetal circulation, truncus arteriosus does not cause any haemodynamic problem in utero. However it is a major problem postnatally and, if left untreated, approximately 80% of infants die within the first year. Diagnosis should be made early by radiologists and cardiologists due to fatal illness. We found it valuable to present a case of truncus arteriosus with computerized tomography findings because of its rare occurrence. |
doi_str_mv | 10.1016/j.radcr.2020.04.007 |
format | article |
fullrecord | <record><control><sourceid>pubmed_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_a547ab45432745d59c2ef3165089f8e5</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1930043320301151</els_id><doaj_id>oai_doaj_org_article_a547ab45432745d59c2ef3165089f8e5</doaj_id><sourcerecordid>32346456</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3577-f6c9131582b841eaae57647f116f0f88febeca766db2cf249efacf7db0d773093</originalsourceid><addsrcrecordid>eNp9kd1qFDEUgAdRbK0-gSB5gR3znxlEoSz-FAre6HXIJCezWXaTIckU-vZmu1raG69yyDnnO8n5uu49wT3BRH7c99k4m3uKKe4x7zFWL7pLMjK8wZyxl0_ii-5NKXuMJRsUed1dMMq45EJedss2xZpNqQjizkQLDtl0XNbagpqOac5m2d0jH6ILcS4oebRALqFUiBXVvEa7FmRyhRxSWcsndI2yydAocYYYqjmgHbQ8cqGAKfC2e-XNocC7v-dV9_vb11_bH5vbn99vtte3G8uEUhsv7UgYEQOdBk7AGBBKcuUJkR77YfAwgTVKSjdR6ykfwRvrlZuwU4rhkV11N2euS2avlxyOJt_rZIJ-uEh51u1VwR5AG8GVmbjgjCounBgtBc-IFHgY_QCisb6cWcs6HcFZOK3s8Az6PBPDTs_pTiuiBkZlA7AzwOZUSgb_2EuwPsnUe_0gU59kasx1k9m6Pjwd-9jzz14r-HwugLbIuwBZFxvgJDFksLX9NPx3wB9afrU2</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Contrast enhanced computed tomography findings of persistent truncus arteriosus; A rare congenital heart disease</title><source>ScienceDirect (Online service)</source><source>PubMed Central</source><creator>Turkoglu, Saim ; Batur, Abdussamet ; Yokuş, Adem ; Dündar, İlyas ; Akinci, Muhammed Bilal</creator><creatorcontrib>Turkoglu, Saim ; Batur, Abdussamet ; Yokuş, Adem ; Dündar, İlyas ; Akinci, Muhammed Bilal</creatorcontrib><description>Persistent Truncus Arteriosus is a cyanotic congenital heart anomaly in which a single trunk supplies both the pulmonary and systemic circulation, instead of a separate aorta and a pulmonary trunk. It is usually classified as a conotruncal anomaly. Due to parallel fetal circulation, truncus arteriosus does not cause any haemodynamic problem in utero. However it is a major problem postnatally and, if left untreated, approximately 80% of infants die within the first year. Diagnosis should be made early by radiologists and cardiologists due to fatal illness. We found it valuable to present a case of truncus arteriosus with computerized tomography findings because of its rare occurrence.</description><identifier>ISSN: 1930-0433</identifier><identifier>EISSN: 1930-0433</identifier><identifier>DOI: 10.1016/j.radcr.2020.04.007</identifier><identifier>PMID: 32346456</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Cardiac ; computerized tomography ; congenital ; heart ; PTA</subject><ispartof>Radiology case reports, 2020-06, Vol.15 (6), p.795-798</ispartof><rights>2020 The Authors</rights><rights>2020 The Authors.</rights><rights>2020 The Authors 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3577-f6c9131582b841eaae57647f116f0f88febeca766db2cf249efacf7db0d773093</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7178326/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1930043320301151$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3535,27903,27904,45759,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32346456$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Turkoglu, Saim</creatorcontrib><creatorcontrib>Batur, Abdussamet</creatorcontrib><creatorcontrib>Yokuş, Adem</creatorcontrib><creatorcontrib>Dündar, İlyas</creatorcontrib><creatorcontrib>Akinci, Muhammed Bilal</creatorcontrib><title>Contrast enhanced computed tomography findings of persistent truncus arteriosus; A rare congenital heart disease</title><title>Radiology case reports</title><addtitle>Radiol Case Rep</addtitle><description>Persistent Truncus Arteriosus is a cyanotic congenital heart anomaly in which a single trunk supplies both the pulmonary and systemic circulation, instead of a separate aorta and a pulmonary trunk. It is usually classified as a conotruncal anomaly. Due to parallel fetal circulation, truncus arteriosus does not cause any haemodynamic problem in utero. However it is a major problem postnatally and, if left untreated, approximately 80% of infants die within the first year. Diagnosis should be made early by radiologists and cardiologists due to fatal illness. We found it valuable to present a case of truncus arteriosus with computerized tomography findings because of its rare occurrence.</description><subject>Cardiac</subject><subject>computerized tomography</subject><subject>congenital</subject><subject>heart</subject><subject>PTA</subject><issn>1930-0433</issn><issn>1930-0433</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kd1qFDEUgAdRbK0-gSB5gR3znxlEoSz-FAre6HXIJCezWXaTIckU-vZmu1raG69yyDnnO8n5uu49wT3BRH7c99k4m3uKKe4x7zFWL7pLMjK8wZyxl0_ii-5NKXuMJRsUed1dMMq45EJedss2xZpNqQjizkQLDtl0XNbagpqOac5m2d0jH6ILcS4oebRALqFUiBXVvEa7FmRyhRxSWcsndI2yydAocYYYqjmgHbQ8cqGAKfC2e-XNocC7v-dV9_vb11_bH5vbn99vtte3G8uEUhsv7UgYEQOdBk7AGBBKcuUJkR77YfAwgTVKSjdR6ykfwRvrlZuwU4rhkV11N2euS2avlxyOJt_rZIJ-uEh51u1VwR5AG8GVmbjgjCounBgtBc-IFHgY_QCisb6cWcs6HcFZOK3s8Az6PBPDTs_pTiuiBkZlA7AzwOZUSgb_2EuwPsnUe_0gU59kasx1k9m6Pjwd-9jzz14r-HwugLbIuwBZFxvgJDFksLX9NPx3wB9afrU2</recordid><startdate>20200601</startdate><enddate>20200601</enddate><creator>Turkoglu, Saim</creator><creator>Batur, Abdussamet</creator><creator>Yokuş, Adem</creator><creator>Dündar, İlyas</creator><creator>Akinci, Muhammed Bilal</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20200601</creationdate><title>Contrast enhanced computed tomography findings of persistent truncus arteriosus; A rare congenital heart disease</title><author>Turkoglu, Saim ; Batur, Abdussamet ; Yokuş, Adem ; Dündar, İlyas ; Akinci, Muhammed Bilal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3577-f6c9131582b841eaae57647f116f0f88febeca766db2cf249efacf7db0d773093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Cardiac</topic><topic>computerized tomography</topic><topic>congenital</topic><topic>heart</topic><topic>PTA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Turkoglu, Saim</creatorcontrib><creatorcontrib>Batur, Abdussamet</creatorcontrib><creatorcontrib>Yokuş, Adem</creatorcontrib><creatorcontrib>Dündar, İlyas</creatorcontrib><creatorcontrib>Akinci, Muhammed Bilal</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Radiology case reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Turkoglu, Saim</au><au>Batur, Abdussamet</au><au>Yokuş, Adem</au><au>Dündar, İlyas</au><au>Akinci, Muhammed Bilal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Contrast enhanced computed tomography findings of persistent truncus arteriosus; A rare congenital heart disease</atitle><jtitle>Radiology case reports</jtitle><addtitle>Radiol Case Rep</addtitle><date>2020-06-01</date><risdate>2020</risdate><volume>15</volume><issue>6</issue><spage>795</spage><epage>798</epage><pages>795-798</pages><issn>1930-0433</issn><eissn>1930-0433</eissn><abstract>Persistent Truncus Arteriosus is a cyanotic congenital heart anomaly in which a single trunk supplies both the pulmonary and systemic circulation, instead of a separate aorta and a pulmonary trunk. It is usually classified as a conotruncal anomaly. Due to parallel fetal circulation, truncus arteriosus does not cause any haemodynamic problem in utero. However it is a major problem postnatally and, if left untreated, approximately 80% of infants die within the first year. Diagnosis should be made early by radiologists and cardiologists due to fatal illness. We found it valuable to present a case of truncus arteriosus with computerized tomography findings because of its rare occurrence.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>32346456</pmid><doi>10.1016/j.radcr.2020.04.007</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1930-0433 |
ispartof | Radiology case reports, 2020-06, Vol.15 (6), p.795-798 |
issn | 1930-0433 1930-0433 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_a547ab45432745d59c2ef3165089f8e5 |
source | ScienceDirect (Online service); PubMed Central |
subjects | Cardiac computerized tomography congenital heart PTA |
title | Contrast enhanced computed tomography findings of persistent truncus arteriosus; A rare congenital heart disease |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T10%3A24%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Contrast%20enhanced%20computed%20tomography%20findings%20of%20persistent%20truncus%20arteriosus;%20A%20rare%20congenital%20heart%20disease&rft.jtitle=Radiology%20case%20reports&rft.au=Turkoglu,%20Saim&rft.date=2020-06-01&rft.volume=15&rft.issue=6&rft.spage=795&rft.epage=798&rft.pages=795-798&rft.issn=1930-0433&rft.eissn=1930-0433&rft_id=info:doi/10.1016/j.radcr.2020.04.007&rft_dat=%3Cpubmed_doaj_%3E32346456%3C/pubmed_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3577-f6c9131582b841eaae57647f116f0f88febeca766db2cf249efacf7db0d773093%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/32346456&rfr_iscdi=true |