Abstract
Langerhans’ cell histiocytosis (LCH) is a rare semimalignant disease in which an uncontrolled proliferation of Langerhans’ cells involves one or more body systems or tissues, leading to different clinical manifestations. Langerhans’ cell histiocytosis nowadays includes diseases previously designated as histiocytosis X, eosinophilic granuloma, Hand-Schüller-Christian syndrome or Abt-Letterer-Siwe disease. Langerhans’ cell histiocytosis usually is considered to be a typical disease of children; nevertheless, many adults are newly diagnosed, and the disease course in children can continue during their adult life. Primary isolated pulmonary Langerhans’ cell histiocytosis, especially in adults, seems to represent a special form of disease [24, 109, 116] requiring specialized (non-radiotherapeutic) treatment and is not addressed in this book chapter.
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Olschewski, T., Seegenschmiedt, M.H., Micke, O. (2008). Langerhans′ Cell Histiocytosis (LCH). In: Seegenschmiedt, M.H., Makoski, HB., Trott, KR., Brady, L.W. (eds) Radiotherapy for Non-Malignant Disorders. Medical Radiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-68943-0_22
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