Lack of bone lesions at diagnosis is associated with inferior outcome in multisystem langerhans cell histiocytosis of childhood

Author:

Aricò Maurizio1,Astigarraga Itziar23,Braier Jorge4,Donadieu Jean5,Gadner Helmut6,Glogova Evgenia6,Grois Nicole6,Henter Jan-Inge7,Janka Gritta8,McClain Kenneth L.9,Ladisch Stephan10,Pötschger Ulrike6,Rosso Diego11,Thiem Elfriede6,Weitzman Sheila12,Windebank Kevin13,Minkov Milen6,

Affiliation:

1. Azienda Sanitaria Provinciale 7; Ragusa Italy

2. Servicio de Pediatria; Bio Cruces Health Research Institute; Hospital Universitario Cruces; Barakaldo Bizkaia Spain

3. Departamento de Pediatria; Universidad del Pais Vasco UPV/EHU; Barakaldo Bizkaia Spain

4. Hospital Nacional de Pediatría J. Garrahan; Buenos Aires Argentina

5. Hospital Trousseau; Paris France

6. Children's Cancer Research Institute and St. Anna Children's Hospital; Vienna Austria

7. Childhood Cancer Research Unit; Karolinska Institutet; Karolinska University Hospital; Stockholm Sweden

8. Department of Haematology and Oncology; University Medical Centre; Hamburg Germany

9. Texas Children's Cancer and Hematology Centers; Houston TX USA

10. Children's Research Institute; Children's National Medical Center; Washington DC USA

11. Hospital de Niños Elizalde and Hospital de Clinicas UBA; Buenos Aires Argentina

12. Hospital for Sick Children; Division of Hematology/Oncology; Toronto ON Canada

13. Newcastle University; Newcastle UK

Publisher

Wiley

Subject

Hematology

Reference32 articles.

1. Clinical aspects of Langerhans cell histiocytosis;Aricò;Hematology Oncology Clinics North of America,1998

2. Langerhans cell histiocytosis in adults. Report from the International Registry of the Histiocyte Society;Aricò;European Journal of Cancer,2003

3. Recurrent BRAF mutations in Langerhans cell histiocytosis;Badalian-Very;Blood,2010

4. Pathogenesis of Langerhans cell histiocytosis;Badalian-Very;Annual Revue Pathology,2013

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