[Kasabach-Merritt syndrome]. / Kasabach Merritt-syndrom.
Ugeskr Laeger
; 156(41): 6011-4, 1994 Oct 10.
Article
en Da
| MEDLINE
| ID: mdl-7992439
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.
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Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Neoplasias del Bazo
/
Trombocitopenia
/
Coagulación Intravascular Diseminada
/
Hemangioma
/
Neoplasias Hepáticas
Tipo de estudio:
Diagnostic_studies
Límite:
Adult
/
Female
/
Humans
Idioma:
Da
Revista:
Ugeskr Laeger
Año:
1994
Tipo del documento:
Article
Pais de publicación:
Dinamarca