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Home/e-Resources/Physiotherapy/Langerhans cell histiocytosis (LCH): Guidelines for diagnosis, clinical work‐up, and treatment for patients till the age of 18 years
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Langerhans cell histiocytosis (LCH): Guidelines for diagnosis, clinical work‐up, and treatment for patients till the age of 18 years

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Abstract & Overview

These guidelines for the management of patients up to 18 years with Langerhans cell histiocytosis (LCH) have been set up by a group of experts involved in the Euro Histio Net project who participated in national or international studies and in peer reviewed publications. Existing guidelines were reviewed and changed where new evidence was available in the literature up to 2012. Data and publications have been ranked according to evidence based medicine and when there was a lack of published data, consensus between experts was sought. Guidelines for diagnosis, initial clinical work-up, and treatment and long-term follow-up of LCH patients are presented.

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Riccardo Haupt, Milen Minkov, Itziar Astigarraga, Eva Schäfer, Vasanta Rao Nanduri, Rima Fuad Jubran, et al. (2012). Langerhans cell histiocytosis (LCH): Guidelines for diagnosis, clinical work‐up, and treatment for patients till the age of 18 years. Pediatric Blood & Cancer, 60(2). https://doi.org/10.1002/pbc.24367

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Haupt, R., Minkov, M., Astigarraga, I., Schäfer, E., Nanduri, V. R., Jubran, R. F., Egeler, R. M., Janka, G., Mićić, D., Rodríguez‐Galindo, C., Gool, S. V., & Visser, J. (2012). Langerhans cell histiocytosis (LCH): Guidelines for diagnosis, clinical work‐up, and treatment for patients till the age of 18 years. Pediatric Blood & Cancer, 60(2). https://doi.org/10.1002/pbc.24367
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