Kasabach-merritt syndrome-associated kaposiform hemangioendothelioma successfully treated with cyclophosphamide, vincristine, and actinomycin D
The authors introduced a successful trial of a chemotherapy regimen to treat refractory thrombocytopenia and pain caused by a rare kaposiform hemangioendothelioma that had been refractory to corticosteroids. A 6-year-old Latina girl with diffuse petechiae, constant pain and edema in her right lower...
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Veröffentlicht in: | Journal of pediatric hematology/oncology 1998-11, Vol.20 (6), p.567-569 |
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