| Literature DB >> 25306933 |
Teruaki Uno1, Shuichi Ito, Atsuko Nakazawa, Osamu Miyazaki, Tetsuya Mori, Keita Terashima.
Abstract
There is currently no consensus on the second-line management of Kaposiform hemangioendothelioma (KHE) that was resistant to prednisolone and vincristine. We described an eight-year-old male with KHE in the right femur that was resistant to prednisolone, vincristine and propranolol. Everolimus, an inhibitor of mammalian target of rapamycin (mTOR) at the dosage of 0.1 mg/kg/day, successfully decreased the tumor size and controlled the symptoms. Everolimus should be further studied as an alternative agent to sirolimus in the management of KHE.Entities:
Keywords: Kasabach-Merritt phenomenon; mTOR; rapamycin; sirolimus; vascular tumor
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Year: 2014 PMID: 25306933 DOI: 10.1002/pbc.25241
Source DB: PubMed Journal: Pediatr Blood Cancer ISSN: 1545-5009 Impact factor: 3.167