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dc.contributor.authorCetinkaya, Merih
dc.contributor.authorDedeoglu, Reyhan
dc.contributor.authorAydogmus, Cigdem
dc.contributor.authorKavuncuoglu, Sultan
dc.contributor.authorTugcu, Deniz
dc.contributor.authorBornaun, Helen
dc.contributor.authorOztarhan, Kazim
dc.contributor.authorErener-Ercan, Tugba
dc.date.accessioned2021-03-04T19:22:54Z
dc.date.available2021-03-04T19:22:54Z
dc.identifier.citationBornaun H., Oztarhan K., Erener-Ercan T., Dedeoglu R., Tugcu D., Aydogmus C., Cetinkaya M., Kavuncuoglu S., "Regression of Cardiac Rhabdomyomas in a Neonate after Everolimus Treatment", CASE REPORTS IN PEDIATRICS, 2016
dc.identifier.othervv_1032021
dc.identifier.otherav_8f76b22e-1264-49fe-90b9-4ae3b67bda34
dc.identifier.urihttp://hdl.handle.net/20.500.12627/96873
dc.identifier.urihttps://doi.org/10.1155/2016/8712962
dc.description.abstractCardiac rhabdomyoma often shows spontaneous regression and usually requires only close follow-up. However, patients with symptomatic inoperable rhabdomyomas may be candidates for everolimus treatment. Our patient had multiple inoperable cardiac rhabdomyomas causing serious left ventricle outflow-tract obstruction that showed a dramatic reduction in the size after everolimus therapy, a mammalian target of rapamycin (mTOR) inhibitor. After discontinuation of therapy, an increase in the diameter of masses occurred and everolimus was restarted. After 6 months of treatment, rhabdomyomas decreased in size and therapy was stopped. In conclusion, everolimus could be a possible novel therapy for neonates with clinically significant rhabdomyomas.
dc.language.isoeng
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectPEDİATRİ
dc.titleRegression of Cardiac Rhabdomyomas in a Neonate after Everolimus Treatment
dc.typeMakale
dc.relation.journalCASE REPORTS IN PEDIATRICS
dc.contributor.departmentKanuni Suleyman Teaching & Res Hosp , ,
dc.contributor.firstauthorID227800


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