Detailed Information

Cited 17 time in webofscience Cited 20 time in scopus
Metadata Downloads

Malignant peripheral nerve sheath tumor arising from the colon in a newborn: report of a case and review of the literatures

Full metadata record
DC Field Value Language
dc.contributor.authorLee, YJ-
dc.contributor.authorMoon, H-
dc.contributor.authorPark, ST-
dc.contributor.authorHa, WS-
dc.contributor.authorChoi, SG-
dc.contributor.authorHong, SC-
dc.contributor.authorJoo, YT-
dc.contributor.authorJeong, CY-
dc.contributor.authorJung, EJ-
dc.date.accessioned2022-12-27T07:34:19Z-
dc.date.available2022-12-27T07:34:19Z-
dc.date.issued2006-02-
dc.identifier.issn0022-3468-
dc.identifier.issn1531-5037-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/29087-
dc.description.abstractA malignant peripheral nerve sheath tumor (MPNST) is a rare neoplasm arising from peripheral nerve sheath. Here, we report the first case of MPNST arising in the colon and also the youngest case of MPNST in the gastrointestinal tract. The patient was a 2-day-old neonate with symptoms and signs of intestinal obstruction. The patient had no family history or stigmata of neurofibromatosis type 1. A computed tomographic scan revealed a 5-cm-sized mass in ascending colon causing intestinal obstruction, and emergent right hemicolectomy was performed. The microscopic examination showed atypical spindle cells with hyperchromatic nuclei and high mitotic activity. The results of immumohistochemical staining, which showed positivity for S-100 and vimentin as well as negativity for smooth muscle actin, CD34, and c-Kit, supported the final diagnosis of MPNST. Genetic analysis of the patient revealed no abnormalities. After surgery, the patient recovered uneventfully and has been free of the disease for 17 months. (c) 2006 Elsevier Inc. All rights reserved.-
dc.language영어-
dc.language.isoENG-
dc.publisherW B SAUNDERS CO-ELSEVIER INC-
dc.titleMalignant peripheral nerve sheath tumor arising from the colon in a newborn: report of a case and review of the literatures-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1016/j.jpedsurg.2005.11.039-
dc.identifier.scopusid2-s2.0-32544436294-
dc.identifier.wosid000236178700044-
dc.identifier.bibliographicCitationJOURNAL OF PEDIATRIC SURGERY, v.41, no.2-
dc.citation.titleJOURNAL OF PEDIATRIC SURGERY-
dc.citation.volume41-
dc.citation.number2-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPediatrics-
dc.relation.journalResearchAreaSurgery-
dc.relation.journalWebOfScienceCategoryPediatrics-
dc.relation.journalWebOfScienceCategorySurgery-
dc.subject.keywordPlusNEUROGENIC SARCOMA-
dc.subject.keywordPlusSCHWANNOMA-
dc.subject.keywordPlusCHILDREN-
dc.subject.keywordPlusSTOMACH-
dc.subject.keywordPlusNEUROFIBROSARCOMA-
dc.subject.keywordPlusEXPERIENCE-
dc.subject.keywordPlusPATIENT-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordAuthormalignant peripheral nerve sheath tumor-
dc.subject.keywordAuthorneonate-
dc.subject.keywordAuthorcolon-
Files in This Item
There are no files associated with this item.
Appears in
Collections
College of Medicine > Department of Medicine > Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Researcher Jung, Eun Jung photo

Jung, Eun Jung
의과대학 (의학과)
Read more

Altmetrics

Total Views & Downloads

BROWSE