Angiosarcoma variant of Kasabach-Merritt syndrome

Citation
C. Alliot et al., Angiosarcoma variant of Kasabach-Merritt syndrome, EUR J GASTR, 13(6), 2001, pp. 731-734
Citations number
25
Categorie Soggetti
Gastroenerology and Hepatology
Journal title
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
ISSN journal
0954691X → ACNP
Volume
13
Issue
6
Year of publication
2001
Pages
731 - 734
Database
ISI
SICI code
0954-691X(200106)13:6<731:AVOKS>2.0.ZU;2-2
Abstract
Kasabach-Merritt syndrome is characterized by the occurrence of disseminate d intravascular coagulation (DIC) usually caused by benign angiomatous tumo urs, Here we report the case of a 70-year-old man in whom DIC revealed a lo cally advanced hepatic tumour. Although DIC resolved with heparin, antithro mbin ill, fresh frozen plasma and corticosteroids, the patient died from ha emoperitoneum following a fall, 3 months after the initial observation, His topathological examination by autopsy allowed the diagnosis of hepatic angi osarcoma. The physiopathogenic mechanisms and treatment options are discuss ed. Eur J Gastroenterol Hepatol 13:731-734 (C) 2001 Lippincott Williams & W ilkins.