Autoimmune Hemolytic Anemia: Diagnosis and Differential Diagnosis.


Journal

Hematology/oncology clinics of North America
ISSN: 1558-1977
Titre abrégé: Hematol Oncol Clin North Am
Pays: United States
ID NLM: 8709473

Informations de publication

Date de publication:
04 2022
Historique:
pubmed: 15 3 2022
medline: 20 4 2022
entrez: 14 3 2022
Statut: ppublish

Résumé

The causes of hemolytic anemia are numerous and a systematic approach is critical for proper identification and classification. The direct antiglobulin test can establish the diagnosis and subclassify the majority of autoimmune hemolytic anemias. Further testing to identify the driver of AIHA can have significant implications in overall management. Advanced testing for rare nonimmune acquired hemolytic anemias or hereditary hemolytic anemias may be necessary if DAT testing is negative.

Identifiants

pubmed: 35282951
pii: S0889-8588(21)00164-7
doi: 10.1016/j.hoc.2021.12.001
pii:
doi:

Substances chimiques

Autoantibodies 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

315-324

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Caleb J Scheckel (CJ)

Division of Hematology, Department of Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA. Electronic address: Scheckel.caleb@mayo.edu.

Ronald S Go (RS)

Division of Hematology, Department of Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

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Classifications MeSH