Summary
Differentials
Common
- Ascaríase
- Estrongiloidíase
- Esquistossomose
- Triquinelose
- Pênfigo
- Penfigoide bolhoso
- Asma
- Eczema
- Rinite alérgica
Uncommon
- Clonorquíase
- Fasciolíase
- Fasciolopsíase
- Opistorquíase
- Filariose
- Gnatostomíase
- Toxocaríase
- Paragonimíase
- infestação de Ancylostoma caninum
- Coccidioidomicose
- Penfigoide gestacional
- Hipersensibilidade medicamentosa
- Erupção cutânea por medicamentos com eosinofilia e sintomas sistêmicos (DRESS)
- Aspergilose broncopulmonar alérgica
- Granulomatose eosinofílica com poliangiite
- Esofagite eosinofílica
- Gastroenterite eosinofílica
- Celulite eosinofílica (síndrome de Wells)
- Leucemia eosinofílica crônica
- Outras leucemias
- Linfoma não Hodgkin
- Linfoma de Hodgkin
- Hipereosinofilia associada à neoplasia não hematológica
- Variante linfocítica da síndrome hipereosinofílica
- Síndrome hipereosinofílica idiopática
- Síndrome de Wiskott-Aldrich
- síndrome de Job
- síndrome de hiperimunoglobulinemia E
- Imunodeficiência grave combinada decorrente de deficiência de adenosina desaminase
- Síndrome de Omenn
- desregulação imune, poliendocrinopatia, enteropatia, síndrome ligada ao cromossomo X (IPEX)
- Síndrome linfoproliferativa autoimune (SLPA)
- Síndrome de Loeys-Dietz
- Síndrome de Comel-Netherton
- Síndrome de dermatite intensa, alergias múltiplas e perda metabólica (SAM)
- Sarcocistose muscular
- Infecção por Cystoisospora belli (anteriormente, Isospora belli)
- Anisaquíase
- Loíase
Contributors
Authors
Barbara J. Bain, MBBS, FRACP, FRCPath
Professor of Diagnostic Haematology
St Mary's Hospital Campus
Imperial College London
London
UK
Disclosures
BJB is an author of a number of references cited in this topic.
James Uprichard, MBBS, BSc, PhD, FRCP, FRCPath
Consultant Haematologist
Department of Haematology
St George's University Hospitals NHS Foundation Trust
London
UK
Disclosures
JU declares that he has no competing interests.
Peer reviewers
Zeinab Afify, MD
Professor of Pediatrics
Department of Pediatrics
Division of Pediatric Hematology Oncology
University of Utah
UT
Disclosures
ZA declares that she has no competing interests.
Jan Cools, PhD
Associate Professor
Department of Molecular and Developmental Genetics
Katholieke Universiteit Leuven
Leuven
Belgium
Disclosures
JC is an author of a reference cited in this topic.
Peer reviewer acknowledgements
BMJ Best Practice topics are updated on a rolling basis in line with developments in evidence and guidance. The peer reviewers listed here have reviewed the content at least once during the history of the topic.
Disclosures
Peer reviewer affiliations and disclosures pertain to the time of the review.
References
Key articles
Valent P, Klion AD, Roufosse F, et al. Proposed refined diagnostic criteria and classification of eosinophil disorders and related syndromes. Allergy. 2023 Jan;78(1):47-59.Full text Abstract
Williams KW, Milner JD, Freeman AF. Eosinophilia associated with disorders of immune deficiency or immune dysregulation. Immunol Allergy Clin North Am. 2015 Aug;35(3):523-44. Abstract
Butt NM, Lambert J, Ali S, et al; British Society for Haematology. Guideline for the investigation and management of eosinophilia. Br J Haematol. 2017 Feb;176(4):553-72.Full text Abstract
Khoury JD, Solary E, Abla O, et al. The 5th edition of the World Health Organization classification of haematolymphoid tumours: myeloid and histiocytic/dendritic neoplasms. Leukemia. 2022 Jul;36(7):1703-19.Full text Abstract
Shomali W, Gotlib J. World Health Organization-defined eosinophilic disorders: 2022 update on diagnosis, risk stratification, and management. Am J Hematol. 2022 Jan 1;97(1):129-48.Full text Abstract
Reference articles
A full list of sources referenced in this topic is available to users with access to all of BMJ Best Practice.
Guidelines
- Good practice paper: the use of genetic tests to diagnose and manage patients with myeloproliferative and myeloproliferative/myelodysplastic neoplasms, and related disorders
- Care program for the diagnosis and treatment of eosinophilia
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