Abstract
© 2014 The Authors. doi: 10.2340/00015555-1807 Journal Compilation © 2014 Acta Dermato-Venereologica. ISSN 0001-5555 Langerhans cell histiocytosis (LCH) is characterised by the clonal proliferation of Langerhans cells (LC) that predominantly occurs in infants and small children, but LCH is rare in adults (1). Generally in children, local therapy would be an appropriate treatment, since patients with localised disease or disease limited to a single organ system have a good prognosis (1). However, the clinical picture of LCH in adults is not fully understood and the optimal treatment for it is still under discussion. In this report, we describe a case of adult onset LCH successfully treated with bi-weekly pegylated interferon (PEG-IFN)α2a and discuss the immunological background focusing on the tumour microenvironment immunologically.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
