| Literature DB >> 23389504 |
Naoko Yasui1, Katsuyoshi Koh, Motohiro Kato, Myoung-ja Park, Daisuke Tomizawa, Koichi Oshima, Naoki Uchisaka, Yoshihiro Gocho, Ayumu Arakawa, Masafumi Seki, Eiji Oguma, Hiroshi Kishimoto, Shoji Watanabe, Akira Kikuchi, Ryoji Hanada.
Abstract
BACKGROUND: Kasabach-Merritt phenomenon (KMP) is a rare condition and optimal treatments have not yet been established, especially for cases that are unresponsive to first-line therapy. We retrospectively reviewed 11 KMP cases treated over the past 13 years in our institute. OBSERVATIONS: With the exception of 1 case, steroids were administered as the first-line therapy. Eight cases required second-line or third-line therapy. The effective salvage therapies include interferon (n=1), radiotherapy (n=1), and chemotherapy (n=5). One case continues to depend upon chemotherapy. Three refractory cases were therapy dependent over 1 year of age, whereas 8 were treated effectively by 6 months of age.Entities:
Mesh:
Year: 2013 PMID: 23389504 DOI: 10.1097/MPH.0b013e318281558e
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289