Use of a Blast Dominance-Hematogone Index for the Flow Cytometric Evaluation of Myelodysplastic Syndrome (MDS).


Journal

American journal of clinical pathology
ISSN: 1943-7722
Titre abrégé: Am J Clin Pathol
Pays: England
ID NLM: 0370470

Informations de publication

Date de publication:
03 05 2019
Historique:
pubmed: 12 3 2019
medline: 14 2 2020
entrez: 12 3 2019
Statut: ppublish

Résumé

We tested whether combined flow cytometric assessment of loss of blast heterogeneity and decreased hematogones is a diagnostically useful approach for evaluation of myelodysplastic syndrome (MDS). Bone marrow samples from patients with known MDS were analyzed by 10-color flow cytometric immunophenotyping and compared with normal bone marrow samples. There was loss of blast heterogeneity in patients with MDS compared with normal bone marrow samples, based on the relative size of the dominant blast population (83.0% vs 64.8%) and fewer hematogones (0.08% vs 1.39%). The size of the largest blast population divided by the fraction of hematogones (blast dominance-hematogone [BDH] index) was significantly larger in MDS compared with normal cases (27,084 vs 190, P < .0001; receiver operating characteristic area under the curve = 0.96). The BDH index is more sensitive and specific than loss of blast heterogeneity or decrease in hematogones for detecting MDS in bone marrow samples and may be useful in clinical practice.

Identifiants

pubmed: 30854558
pii: 5373088
doi: 10.1093/ajcp/aqz004
doi:

Substances chimiques

HLA-DR Antigens 0
CD13 Antigens EC 3.4.11.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

584-592

Informations de copyright

© American Society for Clinical Pathology, 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Jason M Schenkel (JM)

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.

Christopher B Hergott (CB)

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.

Graham Dudley (G)

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.

Mai Drew (M)

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.

Karry Charest (K)

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.

David M Dorfman (DM)

Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA.

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Classifications MeSH