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A Rare Cause of Intestinal Obstruction: Neonatal Gastrointestinal Stromal Tumor

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dc.contributor.authorKOKU, NAİM
dc.contributor.authorTANYERİ, BİLGE
dc.contributor.authorDEMİRCİ, MUSTAFA
dc.contributor.authorKARAKOK, METİN
dc.contributor.authorCITAK, ELVAN CAGLAR
dc.contributor.institutionauthorBAYRAKTAR, BILGE
dc.date.accessioned2019-10-05T23:12:42Z
dc.date.available2019-10-05T23:12:42Z
dc.date.issued2011-02-01
dc.description.abstractGastrointestinal stromal tumors (GISTs) are rare in the childhood period. The authors reported a case who was admitted to the neonatal intensive care unit (NICU) on a suspicion of intestinal obstruction. She was operated and a mass in a size of 6 xx 4.5 xx 4 cm was resected from the ileum. Histologic and immunohistochemical studies showed a GIST. CD34, small muscle actin (SMA), and desmin were positive. The baby was discharged on the 13th day after operation.</.
dc.identifier10.1002/ppul.22740
dc.identifier.citationTANYERİ B., -A Rare Cause of Intestinal Obstruction: Neonatal Gastrointestinal Stromal Tumor-, Pediatric Hematology And Oncology, 2011
dc.identifier.pubmed21299343
dc.identifier.urihttps://hdl.handle.net/20.500.12645/9708
dc.language.isoen
dc.titleA Rare Cause of Intestinal Obstruction: Neonatal Gastrointestinal Stromal Tumor
dc.typeArticle
dspace.entity.typePublication
local.article.journalnamePediatric pulmonology
local.avesis.idf1f661f5-0c11-4963-bfad-036f64613a29
local.avesis.response9582
relation.isAuthorOfPublication0c519bac-cbcb-4931-89f6-451ca267749b
relation.isAuthorOfPublication.latestForDiscovery0c519bac-cbcb-4931-89f6-451ca267749b
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