Abstract
Kasabach Merritt syndrome, first recognized in 1940, is characterized by haemangiomatosis, thrombocytopenia and intravascular coagulation. It is most often seen in children, rarely in adults. The mortality rate is 20-30%. Treatment is by removing the haemangiomatosis and correcting the consumptive coagulopathy. The purpose of this paper is to present a patient with Kasabach Merritt syndrome with haemangiomatosis in the spleen and the liver. A review of the relevant literature is given.
Publication types
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Case Reports
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English Abstract
MeSH terms
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Adult
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Disseminated Intravascular Coagulation* / diagnosis
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Disseminated Intravascular Coagulation* / therapy
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Female
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Hemangioma* / blood
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Hemangioma* / diagnosis
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Hemangioma* / therapy
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Humans
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Liver Neoplasms* / blood
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Liver Neoplasms* / diagnosis
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Liver Neoplasms* / therapy
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Splenic Neoplasms* / blood
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Splenic Neoplasms* / diagnosis
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Splenic Neoplasms* / therapy
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Syndrome
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Thrombocytopenia* / diagnosis
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Thrombocytopenia* / therapy