Patrycja Sosnowska-Sienkiewicz, Zuzanna Nogaj, D. Januszkiewicz-Lewandowska, P. Mańkowski
{"title":"Complex therapy of kaposiform hemangioendothelioma complicated by Kasabach-Merritt syndrome. A case report and review of the literature","authors":"Patrycja Sosnowska-Sienkiewicz, Zuzanna Nogaj, D. Januszkiewicz-Lewandowska, P. Mańkowski","doi":"10.5604/01.3001.0054.4912","DOIUrl":null,"url":null,"abstract":"Background: Kasabach-Merritt syndrome is an infrequent complication of large hemangiomas that could be life-threatening. Ninety percent of this phenomenon is associated with kaposiform hemangioendothelioma. Aim of the study: To present the therapeutic process of a child with kaposiform hemangioendothelioma complicated by this rare syndrome. Case report: The patient was admitted to the hospital during the first month of life due to a lesion on the head and neck. After many attempts with pharmacological treatment, surgery was the only effective treatment.Conclusions: We want to emphasize that operative management of these tumors should be considered in cases of treatment resistance or rapidly progressive growth of the hemangioendothelioma.","PeriodicalId":32604,"journal":{"name":"Medical Science Pulse","volume":"31 4","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical Science Pulse","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5604/01.3001.0054.4912","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Kasabach-Merritt syndrome is an infrequent complication of large hemangiomas that could be life-threatening. Ninety percent of this phenomenon is associated with kaposiform hemangioendothelioma. Aim of the study: To present the therapeutic process of a child with kaposiform hemangioendothelioma complicated by this rare syndrome. Case report: The patient was admitted to the hospital during the first month of life due to a lesion on the head and neck. After many attempts with pharmacological treatment, surgery was the only effective treatment.Conclusions: We want to emphasize that operative management of these tumors should be considered in cases of treatment resistance or rapidly progressive growth of the hemangioendothelioma.