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dc.contributor.author김동원-
dc.date.accessioned2018-07-06T07:10:51Z-
dc.date.available2018-07-06T07:10:51Z-
dc.date.issued2016-06-
dc.identifier.citationWORLD JOURNAL OF PEDIATRICS, v. 12, NO 4, Page. 498-500en_US
dc.identifier.issn1708-8569-
dc.identifier.issn1867-0687-
dc.identifier.urihttps://link.springer.com/article/10.1007%2Fs12519-016-0038-6-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/72420-
dc.description.abstractBackground: Inflammatory myofibroblastic tumor (IMT) is a rare and mostly benign tumor that has the possibility of malignant change. Methods: Radiological findings revealed a huge mass that filled most of the right hemithorax of a 17-month old female infant. Tumor extirpation was stopped due to massive bleeding and limited exposure of the tumor. Embolization was conducted to obstruct the arteries feeding the mass. Complete resection was performed. Results: Histopathologic examination led to the diagnosis of IMT. Postoperative recovery was uneventful. Conclusions: Hypervascularity of IMT should be considered. Preoperative embolization can be effective to reduce intraoperative blood loss and facilitate the surgical procedure.en_US
dc.language.isoenen_US
dc.publisherZHEJIANG UNIV SCH MEDICINEen_US
dc.subjectembolizationen_US
dc.subjectgranulomaen_US
dc.subjectmediastinal neoplasmsen_US
dc.subjectplasma cellen_US
dc.titleComplete resection of a huge hypervascular inflammatory myofibroblastic tumor in right hemithorax after embolizationen_US
dc.typeArticleen_US
dc.relation.no4-
dc.relation.volume12-
dc.identifier.doi10.1007/s12519-016-0038-6-
dc.relation.page498-500-
dc.relation.journalWORLD JOURNAL OF PEDIATRICS-
dc.contributor.googleauthorKim, Kyu-Nam-
dc.contributor.googleauthorKim, Dong-Won-
dc.relation.code2016006189-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.piddongwkim-
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COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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