卡帕斯状血管内皮瘤并发卡萨巴赫-梅里特综合征的复合疗法。病例报告和文献综述

Patrycja Sosnowska-Sienkiewicz, Zuzanna Nogaj, D. Januszkiewicz-Lewandowska, P. Mańkowski
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引用次数: 0

摘要

背景:卡萨巴赫-梅里特综合征是大血管瘤的一种罕见并发症,可能危及生命。90%的这种现象与卡波状血管内皮瘤有关。研究目的介绍一名患有卡波状血管内皮瘤并发这种罕见综合征的儿童的治疗过程。病例报告:患者在出生后的第一个月因头颈部病变入院。在多次尝试药物治疗后,手术是唯一有效的治疗方法:我们想强调的是,在这些肿瘤出现耐药性或快速进展性生长的情况下,应考虑对其进行手术治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Complex therapy of kaposiform hemangioendothelioma complicated by Kasabach-Merritt syndrome. A case report and review of the literature
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.
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