Kaposiform hemangioendothelioma with kasabach-merritt syndrome in a newborn

Annigeri, Venkatesh M.; Pai, Varadraj V.; Dasar, Santosh K.

dc.contributor.author	Annigeri, Venkatesh M.
dc.contributor.author	Pai, Varadraj V.
dc.contributor.author	Dasar, Santosh K.
dc.date.accessioned	2013-02-19T16:25:21Z
dc.date.available	2013-02-19T16:25:21Z
dc.date.issued	2012
dc.identifier.citation	European Journal of Pediatric Dermatology. 2012; 22: 249-52.	en_US
dc.identifier.issn	1122-7672
dc.identifier.uri	http://hdl.handle.net/123456789/390
dc.description.abstract	Kaposiform hemangioendothelioma is a rare vascular tumor and has a high mortality rate in newborns when associated with Kasabach-Merritt syndrome. We present a case of a newborn with a huge lower limb Kaposiform hemangioendothelioma with a rapid tumor growth and a life-threatening Kasabach-Merritt syndrome, which was refractory to medical treatment.	en_US
dc.language.iso	en	en_US
dc.publisher	European Society for Pediatric Dermatology	en_US
dc.subject	Kaposiform hemangioendothelioma	en_US
dc.subject	Kasabach-merritt syndrome	en_US
dc.title	Kaposiform hemangioendothelioma with kasabach-merritt syndrome in a newborn	en_US
dc.type	Article	en_US