Successful Treatment With Interferon Alfa in Infiltrating Angiolipoma: a Case Presenting With Kasabach-merritt Syndrome

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dc.contributor.authorAkyüz, Canan
dc.contributor.authorEmir, Suna
dc.contributor.authorBüyükpamukçu, Münevver
dc.contributor.authorBüyükpamukçu, N.
dc.contributor.authorÇağlar, Meltem
dc.contributor.authorKale, Gülsev
dc.contributor.authorÇalışkan, U.
dc.date.accessioned2020-03-26T16:46:07Z
dc.date.available2020-03-26T16:46:07Z
dc.date.issued2003
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractWe report a case of infiltrating angiolipoma who presented with a large mass on the shoulder and the signs of Kasabach-Merritt syndrome. She improved dramatically within one month and the mass completely disappeared after six months of interferon treatment.en_US
dc.identifier.citationAkyüz, C., Emir, S., Büyükpamukçu, M., Büyükpamukçu, N., Çağlar, M., Kale, G., Çalışkan, U., (2003). Successful Treatment With Interferon Alfa in Infiltrating Angiolipoma: a Case Presenting With Kasabach-merritt Syndrome. Archives of Disease in Childhood, 88(1), 67-68. Doi: 10.1136/adc.88.1.67
dc.identifier.doi10.1136/adc.88.1.67en_US
dc.identifier.endpage68en_US
dc.identifier.issn0003-9888en_US
dc.identifier.issue1en_US
dc.identifier.pmid12495967en_US
dc.identifier.scopusqualityQ1en_US
dc.identifier.startpage67en_US
dc.identifier.urihttps://dx.doi.org/10.1136/adc.88.1.67
dc.identifier.urihttps://hdl.handle.net/20.500.12395/18572
dc.identifier.volume88en_US
dc.identifier.wosWOS:000180231400022en_US
dc.identifier.wosqualityQ1en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherBritish Med Journal Publ Groupen_US
dc.relation.ispartofArchives of Disease in Childhooden_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.selcuk20240510_oaigen_US
dc.titleSuccessful Treatment With Interferon Alfa in Infiltrating Angiolipoma: a Case Presenting With Kasabach-merritt Syndromeen_US
dc.typeArticleen_US

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