| Literature DB >> 21498941 |
Eri Matsuki1, Yuiko Tsukada, Aya Nakaya, Kenji Yokoyama, Shinichiro Okamoto.
Abstract
Adult onset Langerhans cell histiocytosis (LCH) is a rare disorder. Its clinical features have been well described in children, however remain poorly defined in adults. Optimal treatment strategy is still under debate. We have encountered two cases of adult onset LCH, which obtained a durable disease control by combination chemotherapy using prednisone, vinblastine and 6-mercaptopurine. Herein, we report their clinical features together with a review of the current literature.Entities:
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Year: 2011 PMID: 21498941 DOI: 10.2169/internalmedicine.50.4808
Source DB: PubMed Journal: Intern Med ISSN: 0918-2918 Impact factor: 1.271