Resumen
Diferenciales
Común
- Ascariasis
- Strongyloidiasis
- Schistosomiasis
- Trichinellosis
- Pemphigus
- Bullous pemphigoid
- Asthma
- Eczema
- Allergic rhinitis
Infrecuente
- Clonorchiasis
- Fascioliasis
- Fasciolopsiasis
- Opisthorchiasis
- Filariasis
- Gnathostomiasis
- Toxocariasis
- Paragonimiasis
- Ancylostoma caninum infestation
- Coccidioidomycosis
- Pemphigoid gestationis
- Drug hypersensitivity
- Drug rash with eosinophilia and systemic symptoms (DRESS)
- Allergic bronchopulmonary aspergillosis
- Eosinophilic granulomatosis with polyangiitis
- Eosinophilic esophagitis
- Eosinophilic gastroenteritis
- Eosinophilic cellulitis (Wells syndrome)
- Chronic eosinophilic leukemia
- Other leukemias
- Non-Hodgkin lymphoma
- Hodgkin lymphoma
- Nonhematologic malignancy-associated hypereosinophilia
- Lymphocytic variant of hypereosinophilic syndrome
- Idiopathic hypereosinophilic syndrome
- Wiskott-Aldrich syndrome
- Job syndrome
- Hyperimmunoglobulin E syndrome
- Severe combined immune deficiency due to adenosine deaminase deficiency
- Omenn syndrome
- immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome
- Autoimmune lymphoproliferative syndrome (ALPS)
- Loeys-Dietz syndrome
- Comel-Netherton syndrome
- Severe dermatitis, multiple allergies, and metabolic wasting (SAM) syndrome
- Muscular sarcocystosis
- Cystoisospora belli (formerly Isospora belli) infection
- Anisakiasis
- Loiasis
Colaboradores
Autores
Barbara J. Bain, MBBS, FRACP, FRCPath
Professor of Diagnostic Haematology
St Mary's Hospital Campus
Imperial College London
London
UK
Divulgaciones
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
Divulgaciones
JU declares that he has no competing interests.
Revisores por pares
Zeinab Afify, MD
Professor of Pediatrics
Department of Pediatrics
Division of Pediatric Hematology Oncology
University of Utah
UT
Divulgaciones
ZA declares that she has no competing interests.
Jan Cools, PhD
Associate Professor
Department of Molecular and Developmental Genetics
Katholieke Universiteit Leuven
Leuven
Belgium
Divulgaciones
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.
Referencias
Artículos principales
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.Texto completo Resumen
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. Resumen
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.Texto completo Resumen
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.Texto completo Resumen
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.Texto completo Resumen
Artículos de referencia
Una lista completa de las fuentes a las que se hace referencia en este tema está disponible para los usuarios con acceso a todo BMJ Best Practice.
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