Asymptomatic multinodular splenoma

Asymptomatic multinodular splenoma

Splenoma is a rare and benign malformation usually fortuitously diagnosed during imaging, surgery or, unfortunately, at autopsy. Although splenoma was first described in 1861, its association with hematological pathology is a very unusual condition in children. We report the case of an asymptomatic...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International medical case reports journal 2017-01, Vol.10, p.233
Hauptverfasser: Labbe, Sylvain, Elenga, Narcisse, Leduc, Nicolas, Kom-Tchameni, Remi, Long, Laurence, Basset, Thierry, Sika, Anicet, Njuieyon, Falucar, Cuadro, Emma
Format: Artikel
Sprache:eng
Schlagworte:
Care and treatment
Case studies
Diagnosis
Sickle cell anemia
Splenic diseases
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page 233
container_title International medical case reports journal
container_volume 10
creator Labbe, Sylvain
Elenga, Narcisse
Leduc, Nicolas
Kom-Tchameni, Remi
Long, Laurence
Basset, Thierry
Sika, Anicet
Njuieyon, Falucar
Cuadro, Emma
description Splenoma is a rare and benign malformation usually fortuitously diagnosed during imaging, surgery or, unfortunately, at autopsy. Although splenoma was first described in 1861, its association with hematological pathology is a very unusual condition in children. We report the case of an asymptomatic splenoma in an 8-year-old boy with sickle cell anemia, whose diagnosis was confirmed after conventional splenectomy. Keywords: multinodular splenoma, child, sickle cell anemia, conventional splenectomy
format Article
fullrecord <record><control><sourceid>gale</sourceid><recordid>TN_cdi_gale_healthsolutions_A532077786</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A532077786</galeid><sourcerecordid>A532077786</sourcerecordid><originalsourceid>FETCH-gale_healthsolutions_A5320777863</originalsourceid><addsrcrecordid>eNpjYuA0NDS31DU0MYpgQWJzMPAWF2cZAIGxpZG5oTkng5JjcWVuQUl-bmJJZrJCbmlOSWZefkppTmKRQnFBTmoeUIKHgTUtMac4lRdKczOoubmGOHvopifmpMZnpCbmlGQU5-eUlmTm5xXHO5oaGxmYm5tbmBkTrRAAToAzIQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Asymptomatic multinodular splenoma</title><source>DOVE Medical Press Journals</source><source>DOAJ Directory of Open Access Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Labbe, Sylvain ; Elenga, Narcisse ; Leduc, Nicolas ; Kom-Tchameni, Remi ; Long, Laurence ; Basset, Thierry ; Sika, Anicet ; Njuieyon, Falucar ; Cuadro, Emma</creator><creatorcontrib>Labbe, Sylvain ; Elenga, Narcisse ; Leduc, Nicolas ; Kom-Tchameni, Remi ; Long, Laurence ; Basset, Thierry ; Sika, Anicet ; Njuieyon, Falucar ; Cuadro, Emma</creatorcontrib><description>Splenoma is a rare and benign malformation usually fortuitously diagnosed during imaging, surgery or, unfortunately, at autopsy. Although splenoma was first described in 1861, its association with hematological pathology is a very unusual condition in children. We report the case of an asymptomatic splenoma in an 8-year-old boy with sickle cell anemia, whose diagnosis was confirmed after conventional splenectomy. Keywords: multinodular splenoma, child, sickle cell anemia, conventional splenectomy</description><identifier>ISSN: 1179-142X</identifier><identifier>EISSN: 1179-142X</identifier><language>eng</language><publisher>Dove Medical Press Limited</publisher><subject>Care and treatment ; Case studies ; Diagnosis ; Sickle cell anemia ; Splenic diseases</subject><ispartof>International medical case reports journal, 2017-01, Vol.10, p.233</ispartof><rights>COPYRIGHT 2017 Dove Medical Press Limited</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids></links><search><creatorcontrib>Labbe, Sylvain</creatorcontrib><creatorcontrib>Elenga, Narcisse</creatorcontrib><creatorcontrib>Leduc, Nicolas</creatorcontrib><creatorcontrib>Kom-Tchameni, Remi</creatorcontrib><creatorcontrib>Long, Laurence</creatorcontrib><creatorcontrib>Basset, Thierry</creatorcontrib><creatorcontrib>Sika, Anicet</creatorcontrib><creatorcontrib>Njuieyon, Falucar</creatorcontrib><creatorcontrib>Cuadro, Emma</creatorcontrib><title>Asymptomatic multinodular splenoma</title><title>International medical case reports journal</title><description>Splenoma is a rare and benign malformation usually fortuitously diagnosed during imaging, surgery or, unfortunately, at autopsy. Although splenoma was first described in 1861, its association with hematological pathology is a very unusual condition in children. We report the case of an asymptomatic splenoma in an 8-year-old boy with sickle cell anemia, whose diagnosis was confirmed after conventional splenectomy. Keywords: multinodular splenoma, child, sickle cell anemia, conventional splenectomy</description><subject>Care and treatment</subject><subject>Case studies</subject><subject>Diagnosis</subject><subject>Sickle cell anemia</subject><subject>Splenic diseases</subject><issn>1179-142X</issn><issn>1179-142X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNpjYuA0NDS31DU0MYpgQWJzMPAWF2cZAIGxpZG5oTkng5JjcWVuQUl-bmJJZrJCbmlOSWZefkppTmKRQnFBTmoeUIKHgTUtMac4lRdKczOoubmGOHvopifmpMZnpCbmlGQU5-eUlmTm5xXHO5oaGxmYm5tbmBkTrRAAToAzIQ</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Labbe, Sylvain</creator><creator>Elenga, Narcisse</creator><creator>Leduc, Nicolas</creator><creator>Kom-Tchameni, Remi</creator><creator>Long, Laurence</creator><creator>Basset, Thierry</creator><creator>Sika, Anicet</creator><creator>Njuieyon, Falucar</creator><creator>Cuadro, Emma</creator><general>Dove Medical Press Limited</general><scope/></search><sort><creationdate>20170101</creationdate><title>Asymptomatic multinodular splenoma</title><author>Labbe, Sylvain ; Elenga, Narcisse ; Leduc, Nicolas ; Kom-Tchameni, Remi ; Long, Laurence ; Basset, Thierry ; Sika, Anicet ; Njuieyon, Falucar ; Cuadro, Emma</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-gale_healthsolutions_A5320777863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Care and treatment</topic><topic>Case studies</topic><topic>Diagnosis</topic><topic>Sickle cell anemia</topic><topic>Splenic diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Labbe, Sylvain</creatorcontrib><creatorcontrib>Elenga, Narcisse</creatorcontrib><creatorcontrib>Leduc, Nicolas</creatorcontrib><creatorcontrib>Kom-Tchameni, Remi</creatorcontrib><creatorcontrib>Long, Laurence</creatorcontrib><creatorcontrib>Basset, Thierry</creatorcontrib><creatorcontrib>Sika, Anicet</creatorcontrib><creatorcontrib>Njuieyon, Falucar</creatorcontrib><creatorcontrib>Cuadro, Emma</creatorcontrib><jtitle>International medical case reports journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Labbe, Sylvain</au><au>Elenga, Narcisse</au><au>Leduc, Nicolas</au><au>Kom-Tchameni, Remi</au><au>Long, Laurence</au><au>Basset, Thierry</au><au>Sika, Anicet</au><au>Njuieyon, Falucar</au><au>Cuadro, Emma</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Asymptomatic multinodular splenoma</atitle><jtitle>International medical case reports journal</jtitle><date>2017-01-01</date><risdate>2017</risdate><volume>10</volume><spage>233</spage><pages>233-</pages><issn>1179-142X</issn><eissn>1179-142X</eissn><abstract>Splenoma is a rare and benign malformation usually fortuitously diagnosed during imaging, surgery or, unfortunately, at autopsy. Although splenoma was first described in 1861, its association with hematological pathology is a very unusual condition in children. We report the case of an asymptomatic splenoma in an 8-year-old boy with sickle cell anemia, whose diagnosis was confirmed after conventional splenectomy. Keywords: multinodular splenoma, child, sickle cell anemia, conventional splenectomy</abstract><pub>Dove Medical Press Limited</pub></addata></record>
fulltext fulltext
identifier ISSN: 1179-142X
ispartof International medical case reports journal, 2017-01, Vol.10, p.233
issn 1179-142X
1179-142X
language eng
recordid cdi_gale_healthsolutions_A532077786
source DOVE Medical Press Journals; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; PubMed Central Open Access
subjects Care and treatment
Case studies
Diagnosis
Sickle cell anemia
Splenic diseases
title Asymptomatic multinodular splenoma
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T15%3A35%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Asymptomatic%20multinodular%20splenoma&rft.jtitle=International%20medical%20case%20reports%20journal&rft.au=Labbe,%20Sylvain&rft.date=2017-01-01&rft.volume=10&rft.spage=233&rft.pages=233-&rft.issn=1179-142X&rft.eissn=1179-142X&rft_id=info:doi/&rft_dat=%3Cgale%3EA532077786%3C/gale%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rft_galeid=A532077786&rfr_iscdi=true