A case of Kasabach-Merritt syndrome successfully treated by embolization.
نویسندگان
چکیده
منابع مشابه
[A case report of Kasabach-Merritt syndrome].
Kasabach Merritt syndrome (KMS) is an uncommon complication of large haemangioma in which there is thrombocytopenia and coagulopathy. We report a case of a new born male baby presented with a large haemangioma on the right upper extremity and his initial laboratory tests were consistent with consumptive coagulopathy. He was diagnosed as a case of KMS and treated with oral prednisolone. 1. Assoc...
متن کاملKasabach-Merritt syndrome: a case report.
Kasabach-Meritt syndrome is a combination of thromobocytopenia, hemolytic anemia, and acute or chronic consumptive coagulopathy in association with rapidly enlarging hemangioma. A male infant of 5 days was admitted in paediatric ward with this syndrome. The baby had ecchymotic patches over face and extremities and bleeding through umbilical stump. The child expired due to severe thrombocytopeni...
متن کاملKasabach-Merritt syndrome.
Hemangiomas of infancy are usually congenital lesions. Occasionally they are associated with microangiopatbic bemolytic anaemia, thrombocytopenia, and a consumptive coagulopathy. This is most often associated with cavernous hemangiomas. Thrombocytopenia associated with giant cavernous hemangiomas was first noted by Kasabach and Merritt in 1940. As the primary mechanism of platelet destruction i...
متن کاملKasabach-Merritt syndrome associated with angiosarcoma of the scalp successfully treated with chemoradiotherapy.
Sir, Kasabach-Merritt syndrome (KMS) is a condition of consumption coagulopathy in patients bearing vascular tumours and malformations. KMS is seen not only in infants bearing large haemangiomas, but has also been observed in various vascular diseases, such as bluerubber-bleb nevus syndrome (1) and Osler-Weber-Rendu disease (2). Angiosarcoma is a rare malignancy of vascular or lymphatic endothe...
متن کاملKasabach-merritt syndrome arising from tufted angioma successfully treated with systemic corticosteroid.
We report a case of Kasabach-Merritt syndrome arising from a tufted angioma successfully treated with systemic corticosteroid. A 2-month-old male infant presented with a palm-sized, erythematous induration on his left pubis. The lesion was diagnosed as tufted angioma histopathologically. After 1 month, the lesion suddenly expanded to the abdomen and scrotum. Initial laboratory tests were consis...
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ژورنال
عنوان ژورنال: Nihon Shuchu Chiryo Igakukai zasshi
سال: 1999
ISSN: 1340-7988,1882-966X
DOI: 10.3918/jsicm.6.369