Asymptomatic Double Aortic Arch Accidentally Diagnosed for a Child with T-Cell Lymphoma - Case Report
Introduction. Double aortic arch (DAA) represents a vascular malformation generated by the persistence of the right dorsal aorta from the intrauterine life. An aortic ring is formed, that surrounds the trachea and esophagus, resulting in difficulty in breathing and swallowing. Case report. We report...
Gespeichert in:
Veröffentlicht in: | Ars medica tomitana 2018-11, Vol.24 (3), p.157-160 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 160 |
---|---|
container_issue | 3 |
container_start_page | 157 |
container_title | Ars medica tomitana |
container_volume | 24 |
creator | Ioana, Hălmaciu Andrei, Suciu Bogdan Sorin, Roşca Cristina, Nagy Bota Monica Cristian, Trâmbiţaş Klara, Brînzaniuc Adrian, Ivănescu |
description | Introduction. Double aortic arch (DAA) represents a vascular malformation generated by the persistence of the right dorsal aorta from the intrauterine life. An aortic ring is formed, that surrounds the trachea and esophagus, resulting in difficulty in breathing and swallowing.
Case report. We report the case of a 13 years old male child who was admitted to the pediatric surgery department accusing the presence of a paravertebral subcutaneous lesions. Histopathological result of the excised lesion revealed the presence of peripheral T-cell lymphoma. Examination of computer tomography angiography (Angio-CT) revealed the presence of a complete arterial chain (aortic double arch - DAA) around the trachea and esophagus, without signs of compression.
Most cases are diagnosed in the first year of life, the literature reports a few cases of DAA diagnosed late, to the adolescent or adult. Clinically most of the anatomical variants are usually symptomatic especially that are associated with congenital heart defects, including also Fallot tetralogy.
Conclusions. Angio-CT is a very useful method in diagnosing arterial or venous malformations, symptomatic or asymptomatic. |
doi_str_mv | 10.2478/arsm-2018-0028 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_crossref_primary_10_2478_arsm_2018_0028</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3155833019</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1607-b1b10c0473ca08bf71049fee99bbcd0785efc4c852d0e36de708e5f0978107ed3</originalsourceid><addsrcrecordid>eNptkM1LxDAUxIsouOhePQc8d31p2k0KXkrXL1gQZD2XNHnddkk3NWlZ-t_bsoIePL15MPMbmCC4o7CKYi4epPNtGAEVIUAkLoIFFTENY2Dryz_6Olh6fwAAypmgUboIMPNj2_W2lX2jyMYOpUGSWTd_mVM1yZRqNB57acxINo3cH61HTSrriCR53RhNTk1fk12YozFkO9HqiUZCkkuP5AO7CXYbXFXSeFz-3Jvg8_lpl7-G2_eXtzzbhoqugYclLSkoiDlTEkRZcQpxWiGmaVkqDVwkWKlYiSTSgGytkYPApIKUCwocNbsJ7s_cztmvAX1fHOzgjlNlwWiSCMaAppNrdXYpZ713WBWda1rpxoJCMa9ZzGsW85rFvOYUeDwHTtL06DTu3TBO4pf-fzCKp1bOvgFAT3tH</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3155833019</pqid></control><display><type>article</type><title>Asymptomatic Double Aortic Arch Accidentally Diagnosed for a Child with T-Cell Lymphoma - Case Report</title><source>De Gruyter Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Ioana, Hălmaciu ; Andrei, Suciu Bogdan ; Sorin, Roşca ; Cristina, Nagy Bota Monica ; Cristian, Trâmbiţaş ; Klara, Brînzaniuc ; Adrian, Ivănescu</creator><creatorcontrib>Ioana, Hălmaciu ; Andrei, Suciu Bogdan ; Sorin, Roşca ; Cristina, Nagy Bota Monica ; Cristian, Trâmbiţaş ; Klara, Brînzaniuc ; Adrian, Ivănescu</creatorcontrib><description>Introduction. Double aortic arch (DAA) represents a vascular malformation generated by the persistence of the right dorsal aorta from the intrauterine life. An aortic ring is formed, that surrounds the trachea and esophagus, resulting in difficulty in breathing and swallowing.
Case report. We report the case of a 13 years old male child who was admitted to the pediatric surgery department accusing the presence of a paravertebral subcutaneous lesions. Histopathological result of the excised lesion revealed the presence of peripheral T-cell lymphoma. Examination of computer tomography angiography (Angio-CT) revealed the presence of a complete arterial chain (aortic double arch - DAA) around the trachea and esophagus, without signs of compression.
Most cases are diagnosed in the first year of life, the literature reports a few cases of DAA diagnosed late, to the adolescent or adult. Clinically most of the anatomical variants are usually symptomatic especially that are associated with congenital heart defects, including also Fallot tetralogy.
Conclusions. Angio-CT is a very useful method in diagnosing arterial or venous malformations, symptomatic or asymptomatic.</description><identifier>ISSN: 1841-4036</identifier><identifier>ISSN: 1223-9666</identifier><identifier>EISSN: 1841-4036</identifier><identifier>DOI: 10.2478/arsm-2018-0028</identifier><language>eng</language><publisher>Constanţa: Sciendo</publisher><subject>Asymptomatic ; Case reports ; CT angiography ; double aortic arch ; Esophagus ; Lymphoma</subject><ispartof>Ars medica tomitana, 2018-11, Vol.24 (3), p.157-160</ispartof><rights>2018. This work is published under http://creativecommons.org/licenses/by-nc-nd/3.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1607-b1b10c0473ca08bf71049fee99bbcd0785efc4c852d0e36de708e5f0978107ed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://sciendo.com/pdf/10.2478/arsm-2018-0028$$EPDF$$P50$$Gwalterdegruyter$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://sciendo.com/article/10.2478/arsm-2018-0028$$EHTML$$P50$$Gwalterdegruyter$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,27901,27902,75907,75908</link.rule.ids></links><search><creatorcontrib>Ioana, Hălmaciu</creatorcontrib><creatorcontrib>Andrei, Suciu Bogdan</creatorcontrib><creatorcontrib>Sorin, Roşca</creatorcontrib><creatorcontrib>Cristina, Nagy Bota Monica</creatorcontrib><creatorcontrib>Cristian, Trâmbiţaş</creatorcontrib><creatorcontrib>Klara, Brînzaniuc</creatorcontrib><creatorcontrib>Adrian, Ivănescu</creatorcontrib><title>Asymptomatic Double Aortic Arch Accidentally Diagnosed for a Child with T-Cell Lymphoma - Case Report</title><title>Ars medica tomitana</title><description>Introduction. Double aortic arch (DAA) represents a vascular malformation generated by the persistence of the right dorsal aorta from the intrauterine life. An aortic ring is formed, that surrounds the trachea and esophagus, resulting in difficulty in breathing and swallowing.
Case report. We report the case of a 13 years old male child who was admitted to the pediatric surgery department accusing the presence of a paravertebral subcutaneous lesions. Histopathological result of the excised lesion revealed the presence of peripheral T-cell lymphoma. Examination of computer tomography angiography (Angio-CT) revealed the presence of a complete arterial chain (aortic double arch - DAA) around the trachea and esophagus, without signs of compression.
Most cases are diagnosed in the first year of life, the literature reports a few cases of DAA diagnosed late, to the adolescent or adult. Clinically most of the anatomical variants are usually symptomatic especially that are associated with congenital heart defects, including also Fallot tetralogy.
Conclusions. Angio-CT is a very useful method in diagnosing arterial or venous malformations, symptomatic or asymptomatic.</description><subject>Asymptomatic</subject><subject>Case reports</subject><subject>CT angiography</subject><subject>double aortic arch</subject><subject>Esophagus</subject><subject>Lymphoma</subject><issn>1841-4036</issn><issn>1223-9666</issn><issn>1841-4036</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNptkM1LxDAUxIsouOhePQc8d31p2k0KXkrXL1gQZD2XNHnddkk3NWlZ-t_bsoIePL15MPMbmCC4o7CKYi4epPNtGAEVIUAkLoIFFTENY2Dryz_6Olh6fwAAypmgUboIMPNj2_W2lX2jyMYOpUGSWTd_mVM1yZRqNB57acxINo3cH61HTSrriCR53RhNTk1fk12YozFkO9HqiUZCkkuP5AO7CXYbXFXSeFz-3Jvg8_lpl7-G2_eXtzzbhoqugYclLSkoiDlTEkRZcQpxWiGmaVkqDVwkWKlYiSTSgGytkYPApIKUCwocNbsJ7s_cztmvAX1fHOzgjlNlwWiSCMaAppNrdXYpZ713WBWda1rpxoJCMa9ZzGsW85rFvOYUeDwHTtL06DTu3TBO4pf-fzCKp1bOvgFAT3tH</recordid><startdate>20181101</startdate><enddate>20181101</enddate><creator>Ioana, Hălmaciu</creator><creator>Andrei, Suciu Bogdan</creator><creator>Sorin, Roşca</creator><creator>Cristina, Nagy Bota Monica</creator><creator>Cristian, Trâmbiţaş</creator><creator>Klara, Brînzaniuc</creator><creator>Adrian, Ivănescu</creator><general>Sciendo</general><general>De Gruyter Poland</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20181101</creationdate><title>Asymptomatic Double Aortic Arch Accidentally Diagnosed for a Child with T-Cell Lymphoma - Case Report</title><author>Ioana, Hălmaciu ; Andrei, Suciu Bogdan ; Sorin, Roşca ; Cristina, Nagy Bota Monica ; Cristian, Trâmbiţaş ; Klara, Brînzaniuc ; Adrian, Ivănescu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1607-b1b10c0473ca08bf71049fee99bbcd0785efc4c852d0e36de708e5f0978107ed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Asymptomatic</topic><topic>Case reports</topic><topic>CT angiography</topic><topic>double aortic arch</topic><topic>Esophagus</topic><topic>Lymphoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ioana, Hălmaciu</creatorcontrib><creatorcontrib>Andrei, Suciu Bogdan</creatorcontrib><creatorcontrib>Sorin, Roşca</creatorcontrib><creatorcontrib>Cristina, Nagy Bota Monica</creatorcontrib><creatorcontrib>Cristian, Trâmbiţaş</creatorcontrib><creatorcontrib>Klara, Brînzaniuc</creatorcontrib><creatorcontrib>Adrian, Ivănescu</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Publicly Available Content Database</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><jtitle>Ars medica tomitana</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ioana, Hălmaciu</au><au>Andrei, Suciu Bogdan</au><au>Sorin, Roşca</au><au>Cristina, Nagy Bota Monica</au><au>Cristian, Trâmbiţaş</au><au>Klara, Brînzaniuc</au><au>Adrian, Ivănescu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Asymptomatic Double Aortic Arch Accidentally Diagnosed for a Child with T-Cell Lymphoma - Case Report</atitle><jtitle>Ars medica tomitana</jtitle><date>2018-11-01</date><risdate>2018</risdate><volume>24</volume><issue>3</issue><spage>157</spage><epage>160</epage><pages>157-160</pages><issn>1841-4036</issn><issn>1223-9666</issn><eissn>1841-4036</eissn><abstract>Introduction. Double aortic arch (DAA) represents a vascular malformation generated by the persistence of the right dorsal aorta from the intrauterine life. An aortic ring is formed, that surrounds the trachea and esophagus, resulting in difficulty in breathing and swallowing.
Case report. We report the case of a 13 years old male child who was admitted to the pediatric surgery department accusing the presence of a paravertebral subcutaneous lesions. Histopathological result of the excised lesion revealed the presence of peripheral T-cell lymphoma. Examination of computer tomography angiography (Angio-CT) revealed the presence of a complete arterial chain (aortic double arch - DAA) around the trachea and esophagus, without signs of compression.
Most cases are diagnosed in the first year of life, the literature reports a few cases of DAA diagnosed late, to the adolescent or adult. Clinically most of the anatomical variants are usually symptomatic especially that are associated with congenital heart defects, including also Fallot tetralogy.
Conclusions. Angio-CT is a very useful method in diagnosing arterial or venous malformations, symptomatic or asymptomatic.</abstract><cop>Constanţa</cop><pub>Sciendo</pub><doi>10.2478/arsm-2018-0028</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1841-4036 |
ispartof | Ars medica tomitana, 2018-11, Vol.24 (3), p.157-160 |
issn | 1841-4036 1223-9666 1841-4036 |
language | eng |
recordid | cdi_crossref_primary_10_2478_arsm_2018_0028 |
source | De Gruyter Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Asymptomatic Case reports CT angiography double aortic arch Esophagus Lymphoma |
title | Asymptomatic Double Aortic Arch Accidentally Diagnosed for a Child with T-Cell Lymphoma - Case Report |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T10%3A55%3A11IST&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=Asymptomatic%20Double%20Aortic%20Arch%20Accidentally%20Diagnosed%20for%20a%20Child%20with%20T-Cell%20Lymphoma%20-%20Case%20Report&rft.jtitle=Ars%20medica%20tomitana&rft.au=Ioana,%20H%C4%83lmaciu&rft.date=2018-11-01&rft.volume=24&rft.issue=3&rft.spage=157&rft.epage=160&rft.pages=157-160&rft.issn=1841-4036&rft.eissn=1841-4036&rft_id=info:doi/10.2478/arsm-2018-0028&rft_dat=%3Cproquest_cross%3E3155833019%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=3155833019&rft_id=info:pmid/&rfr_iscdi=true |