Kasabach-Merritt syndrome

(redirected from Hemangioma thrombocytopenia syndrome)

Kas·a·bach-Mer·ritt syn·drome

(kas'ă-bahk mer'it),
thrombocytopenia and consumptive coagulopathy developing in a large hemangioma, usually in early infancy.

Kas·a·bach-Mer·ritt syn·drome

(kahs'ă-bok-mer'it sin'drōm)
Large, bluish, progressive vascular malformations in extremities. Stagnation of blood in lesions can cause disseminated intravascular coagulation, platelet consumption, and bleeding. Condition usually affects infants; sudden growth of lesion causes depletion of platelets. Mortality rate is around 30%.

Kasabach,

Haig H., U.S. physician, 1898-1943.
Kasabach-Merritt syndrome - capillary hemangioma associated with thrombocytopenic purpura. Synonym(s): hemangioma-thrombocytopenia syndrome

Merritt,

Katharine Krom, U.S. pediatrician, 1886–.
Kasabach-Merritt syndrome - see under Kasabach
References in periodicals archive ?
(1) It is also known as Hemangioma thrombocytopenia syndrome. It carries the names of Dr Haig Haigouni Kasabach and Dr Katharine Krom Merritt, the two pediatricians who first described the condition in 1940.