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Angiosarcoma variant of Kasabach-Merritt syndrome.
Alliot, C; Tribout, B; Barrios, M; Gontier, M F.
Affiliation
  • Alliot C; Department of Haematology, University Hospital of Amiens, France.
Eur J Gastroenterol Hepatol ; 13(6): 731-4, 2001 Jun.
Article in En | MEDLINE | ID: mdl-11434603
Kasabach-Merritt syndrome is characterized by the occurrence of disseminated intravascular coagulation (DIC) usually caused by benign angiomatous tumours. Here we report the case of a 70-year-old man in whom DIC revealed a locally advanced hepatic tumour. Although DIC resolved with heparin, antithrombin III, fresh frozen plasma and corticosteroids, the patient died from haemoperitoneum following a fall, 3 months after the initial observation. Histopathological examination by autopsy allowed the diagnosis of hepatic angiosarcoma. The physiopathogenic mechanisms and treatment options are discussed.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Disseminated Intravascular Coagulation / Hemangiosarcoma / Liver Neoplasms Type of study: Diagnostic_studies Limits: Aged / Humans / Male Language: En Journal: Eur J Gastroenterol Hepatol Journal subject: GASTROENTEROLOGIA Year: 2001 Document type: Article Affiliation country: France Country of publication: United kingdom
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Collection: 01-internacional Database: MEDLINE Main subject: Disseminated Intravascular Coagulation / Hemangiosarcoma / Liver Neoplasms Type of study: Diagnostic_studies Limits: Aged / Humans / Male Language: En Journal: Eur J Gastroenterol Hepatol Journal subject: GASTROENTEROLOGIA Year: 2001 Document type: Article Affiliation country: France Country of publication: United kingdom