Avaliação da eosinofilia

Last reviewed: 21 Aug 2025
Last updated: 31 Dec 2024

Summary

Differentials

Common

  • Ascaríase
  • Estrongiloidíase
  • Esquistossomose
  • Triquinelose
  • Pênfigo
  • Penfigoide bolhoso
  • Asma
  • Eczema
  • Rinite alérgica
Full details

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
Full details

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

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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.
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  • Guidelines

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