Bozkaya Halil, Cinar Celal, Ünalp Ömer Vedat, Parildar Mustafa, Oran Ismail
Department of Radiology, Division of Interventional Radiology, Ege University, School of Medicine, 35100, Izmir, Turkey,
Wien Klin Wochenschr. 2015 Jun;127(11-12):488-90. doi: 10.1007/s00508-014-0675-5. Epub 2014 Dec 4.
Kasabach-Merritt syndrome (KMS) is a rare complication of cavernous hemangiomas characterized with anemia, thrombocytopenia, and consumption coagulopathy. This syndrome usually develops due to superficial soft tissue hemangiomas in infancy and childhood. KMS developing secondarily to hepatic hemangioma is very rare. In this report, we aimed to present the treatment of KMS developing secondarily to giant cavernous hemangioma of the liver with transarterial chemoembolization using bleomycin.
卡萨巴赫-梅里特综合征(KMS)是海绵状血管瘤的一种罕见并发症,其特征为贫血、血小板减少和消耗性凝血病。该综合征通常因婴幼儿期和儿童期的浅表软组织血管瘤发展而来。继发于肝血管瘤的KMS非常罕见。在本报告中,我们旨在介绍使用博来霉素经动脉化疗栓塞治疗继发于肝脏巨大海绵状血管瘤的KMS。