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dc.contributor.authorTolgay, E
dc.contributor.authorKoc, S
dc.contributor.authorOz, B
dc.contributor.authorYilmaz, Ravza Sümeyye
dc.contributor.authorAkyildiz, EU
dc.date.accessioned2021-03-03T11:50:29Z
dc.date.available2021-03-03T11:50:29Z
dc.date.issued2006
dc.identifier.citationAkyildiz E., Tolgay E., Oz B., Yilmaz R. S. , Koc S., "Cardiac myxoma: an unusual cause of sudden death in childhood", TURKISH JOURNAL OF PEDIATRICS, cilt.48, sa.2, ss.172-174, 2006
dc.identifier.issn0041-4301
dc.identifier.othervv_1032021
dc.identifier.otherav_2a5333f5-0a87-4155-b2da-850cdc8c6a0e
dc.identifier.urihttp://hdl.handle.net/20.500.12627/33238
dc.description.abstractPrimary tumors of the heart and pericardium are rare in autopsy series. Considering all age groups, the most common cardiac tumor is the myxoma. They may arise in any of the four chambers or, rarely, on the heart valves. About 90% are located in the atria, with the left-to-right ratio of 4:1. The majority of patients are usually in the age group of 30-60 years. Female predominance has been reported. In this report, we describe a six-year-old boy with right atrial myxoma. A 5x4x3 cm, polypoid, smooth-surfaced, brown-colored tumor was found in the right atrium. It was attached by the stalk to the atrial septum. Microscopically, the tumor had the typical appearance of a myxoma with spindle cells widely spaced by abundant myxoid matrix. The diagnosis was based on histopathological and immunohistochemical findings.
dc.language.isoeng
dc.subjectTıp
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleCardiac myxoma: an unusual cause of sudden death in childhood
dc.typeMakale
dc.relation.journalTURKISH JOURNAL OF PEDIATRICS
dc.contributor.department, ,
dc.identifier.volume48
dc.identifier.issue2
dc.identifier.startpage172
dc.identifier.endpage174
dc.contributor.firstauthorID27247


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