The medical recommendations for adult LCH have been published in Orphanet Journal of Rare Diseases.

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An­nu­al in­ter­na­tio­nal con­fe­rence of sci­en­tists, pa­tho­lo­gists and cli­ni­ci­ans discussing histiocytoses and their backgrounds. More ...
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European Union Clinical Trials Register of the European Medicines Agency

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European Clinical Trials Database of the European Medicines Agency

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Rare diseases in EU
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Management algorithm

Author(s): Euro Histio Net Work Group for LCH Guidelines for adults (see introduction page), Created: 2012/07/26, last update: 2013/08/18

Treatment recommendations are based on site and extension of the disease. Children must not be treated according to these recommendations (see childhood LCH).

Figure 1 Management of Langerhans Cell Histiocytosis in adults.