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Coronavirus disease 2019 (COVID‐19): Focus on peripheral blood cell morphology.

Authors :
Zini, Gina
d'Onofrio, Giuseppe
Source :
British Journal of Haematology. Feb2023, Vol. 200 Issue 4, p404-419. 16p.
Publication Year :
2023

Abstract

Summary: Numerous studies have shown peculiar morphological anomalies in COVID‐19 patients' smears. We searched all the peer‐reviewed scientific publications that explicitly reference the cytomorphological alterations on peripheral blood smears of patients with COVID‐19. We extracted data from sixty‐five publications (case reports, patient group studies, reviews, and erythrocyte morphology studies). The results show that frequent alterations concern the morphology of lymphocytes (large lymphocytes with weakly basophilic cytoplasm, plasmacytoid lymphocytes, large granular lymphocytes). Neutrophils display abnormal nuclei and cytoplasm in a distinctive cytomorphological picture. Besides a left shift in maturation, granulations can be increased (toxic type) or decreased with areas of basophilia. Nuclei are often hyposegmented (pseudo‐Pelger‐Huёt anomaly). Apoptotic or pycnotic cells are not uncommon. Monocytes typically have a large cytoplasm loaded with heterogeneous and coalescing vacuoles. Platelets show large and giant shapes. The presence of erythrocyte fragments and schistocytes is especially evident in the forms of COVID‐19 that are associated with thrombotic microangiopathies. Such atypia of blood cells reflects the generalized activation in severe COVID‐19, which has been demonstrated with immunophenotypic, molecular, genetic, and functional methods. Neutrophils, in particular, are involved in the pathophysiology of hyperinflammation with cytokine storm, which characterizes the most unfavorable evolution. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00071048
Volume :
200
Issue :
4
Database :
Academic Search Index
Journal :
British Journal of Haematology
Publication Type :
Academic Journal
Accession number :
161689962
Full Text :
https://doi.org/10.1111/bjh.18489