How I investigate neutropenia
- PMID: 32543073
- DOI: 10.1111/ijlh.13210
How I investigate neutropenia
Abstract
Neutropenia is a common laboratory finding in adults and children. Its underlying causes are extremely heterogeneous and include benign conditions, autoimmune disorders, infections, and malignancies. The clinical laboratory plays a central role in the diagnosis of these disorders, including data derived from hematology, microbiology, molecular biology/cytogenetics, and clinical chemistry. The purpose of this review is to (a) highlight the clinical, hematologic, and molecular genetic features of the major entities resulting in neutropenia and (b) outline an algorithm-based approach to permit the classification of neutropenias.
Keywords: neutropenia; neutrophils.
© 2020 John Wiley & Sons Ltd.
References
REFERENCES
-
- Rodak's Hematology: Clinical Principles and Applications (5th edn). St. Louis, MO: Elsevier; 2016.
-
- Denic S, Showqi S, Klein C, Takala M, Nagelkerke N, Agarwal MM. Prevalence, phenotype and inheritance of benign neutropenia in Arabs. BMC Blood Disord. 2009;9:3.
-
- Haddy TB, Rana SR, Castro O. Benign ethnic neutropenia: what is a normal absolute neutrophil count? J Lab Clin Med. 1999;133(1):15-22.
-
- Joyce RA, Boggs DR, Hasiba U, Srodes CH. Marginal neutrophil pool size in normal subjects and neutropenic patients as measured by epinephrine infusion. J Lab Clin Med. 1976;88(4):614-620.
-
- Galifi M, Schinella M, Nicoli M, Lippi G. Instrumental reports and effect of anticoagulants in a case of neutrophil agglutination in vitro. Haematologica. 1993;78(6):364-370.
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