
The Kasabach-Merritt syndrome is a rare, congenital disease, characterized by giant haemangiomatosis and disseminated intravasal coagulation. It is reported on an at present 34-year-old patient with such a disease and the long-term course is described. Complications with haemorrhages can be prevented by means of anticoagulants.
Adult, Male, Neoplasms, Multiple Primary, Disability Evaluation, Hemangioma, Cavernous, Skin Neoplasms, Humans, Blood Coagulation Tests, Syndrome, Disseminated Intravascular Coagulation, Hemangioma, Thrombocytopenia
Adult, Male, Neoplasms, Multiple Primary, Disability Evaluation, Hemangioma, Cavernous, Skin Neoplasms, Humans, Blood Coagulation Tests, Syndrome, Disseminated Intravascular Coagulation, Hemangioma, Thrombocytopenia
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