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Improved outcome in the treatment of pediatric multifocal Langerhans cell histiocytosis : Results from the Japan Langerhans Cell Histiocytosis Study Group-96 protocol study

✍ Scribed by Akira Morimoto; Satoshi Ikushima; Naoko Kinugawa; Eiichi Ishii; Urara Kohdera; Masahiro Sako; Junichiro Fujimoto; Fumio Bessho; Keizo Horibe; Yukiko Tsunematsu; Shinsaku Imashuku; for the Japan Langerhans Cell Histiocytosis Study Group

Publisher: John Wiley and Sons
Year: 2006
Tongue: English
Weight: 194 KB
Volume: 107
Category: Article
ISSN: 0008-543X
DOI: 10.1002/cncr.21985

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## Abstract ## Background Single‐system (SS) disease is the most common presentation in Langerhans cell histiocytosis (LCH) with a heterogenous clinical picture and course. Mostly bone and rarely skin or lymph nodes are involved. ## Procedure One hundred and seventy patients with SS‐LCH were reg