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- W2023132371 abstract "Fig. 1. (A) Tufted angioma involving the chin in a one-month-old child. (B) The patient at 2 months of age showing a subtle increase in tumour size and decrease in platelet count. (C) A subtle residual lesion on the chin of the patient at the age of 5 years. Tufted angioma (TA) is an infrequently seen, benign vascular tumour, which was first described in 1949 (1). It is characterized clinically by a solitary tumour or infiltrated plaque thought to have a more inflammatory appearance than vascular. The great majority appear during the first 5 years of life; however, rare cases of TA presenting at birth have been noted (2, 3). Kasabach-Merritt phenomenon (KMP) is a form of microangiopathic haemolysis, with coagulopathy related to the sequestration of platelets and coagulation factors within the tumour. The sequestration creates a form of disseminated intravascular coagulation, with the patients having both a propensity to clotting and a high risk of bleeding. It is an infrequent complication of TA, which represents a therapeutic challenge (4)." @default.
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- W2023132371 date "2010-01-01" @default.
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- W2023132371 title "Tufted Angioma Associated with Kasabach-Merritt Phenomenon: A Therapeutic Challenge" @default.
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- W2023132371 doi "https://doi.org/10.2340/00015555-0848" @default.
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