| Literature DB >> 26907642 |
Hideki Matsumoto1, Michio Ozeki, Tomohiro Hori, Kaori Kanda, Norio Kawamoto, Akihito Nagano, Eiichi Azuma, Tatsuhiko Miyazaki, Toshiyuki Fukao.
Abstract
Kasabach-Merritt phenomenon (KMP) is a life-threatening consumptive coagulopathy associated with underlying kaposiform hemangioendothelioma (KHE) in infancy. We describe the case of a 3-month-old girl with KHE complicated by KMP who responded dramatically to treatment with everolimus, a mechanistic target of rapamycin (mTOR) inhibitor. Immunohistochemical expression of mTOR was found in the KHE biopsy specimens, which may explain the improvement of KMP and reduction in KHE tumor size with mTOR inhibitor treatment. This effective use of everolimus may shed light on the emerging role of mTOR signaling in the development and pathogenesis of KHE and KMP.Entities:
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Year: 2016 PMID: 26907642 DOI: 10.1097/MPH.0000000000000509
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289