Incidence, prevalence and survival in patients with Langerhans cell histiocytosis: A national registry study from England, 2013–2019

Author:

Liu Hanhua1ORCID,Stiller Charles A.1,Crooks Colin J.2,Rous Brian1,Bythell Mary1,Broggio John1,Rankin Judith3,Nanduri Vasanta4,Lanyon Peter5,Card Tim R.5,Ban Lu6,Elliss‐Brookes Lucy1,Broughan Jennifer M.1,Paley Lizz1,Wong Kwok1,Bacon Andrew1,Bishton Mark7ORCID,West Joe5ORCID

Affiliation:

1. National Disease Registration Service NHS Digital Leeds UK

2. NIHR Nottingham Biomedical Research Centre University of Nottingham Nottingham UK

3. Population Health Sciences Institute Newcastle University Newcastle upon Tyne UK

4. Watford General Hospital Watford UK

5. Lifespan and Population Health University of Nottingham Nottingham UK

6. Nottingham Digestive Diseases Centre University of Nottingham Nottingham UK

7. Department of Haematology Nottingham City Hospital Nottingham UK

Publisher

Wiley

Subject

Hematology

Reference41 articles.

1. Histiocytosis X; integration of eosinophilic granuloma of bone, letterer‐Siwe disease, and Schüller‐Christian disease as related manifestations of a single nosologic entity;Lichtenstein L;AMA Arch Pathol,1953

2. Histiocytosis syndromes in children;Writing Group of the Histiocyte Society;Lancet,1987

3. Langerhans'-Cell Histiocytosis (Histiocytosis X) -- A Clonal Proliferative Disease

4. Recurrent BRAF mutations in Langerhans cell histiocytosis

5. Histiocytosis

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