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

Identifieur interne : 000093 ( Istex/Corpus ); précédent : 000092; suivant : 000094

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

Auteurs : Riccardo Haupt ; Milen Minkov ; Itziar Astigarraga ; Eva Sch Fer ; Vasanta Nanduri ; Rima Jubran ; R. Maarten Egeler ; Gritta Janka ; Dragan Micic ; Carlos Rodriguez-Galindo ; Stefaan Van Gool ; Johannes Visser ; Sheila Weitzman ; Jean Donadieu

Source :

RBID : ISTEX:04AF7C0F91AFDA48174DBCF78A4FF3B37FF99CA2

English descriptors

Abstract

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. Pediatr Blood Cancer 2013;60:175–184. © 2012 The Authors. Pediatric Blood & Cancer, published by Wiley Periodicals, Inc.

Url:
DOI: 10.1002/pbc.24367

Links to Exploration step

ISTEX:04AF7C0F91AFDA48174DBCF78A4FF3B37FF99CA2

Le document en format XML

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<div type="abstract" xml:lang="en">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. Pediatr Blood Cancer 2013;60:175–184. © 2012 The Authors. Pediatric Blood & Cancer, published by Wiley Periodicals, Inc.</div>
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