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Megakaryocyte ploidy in thrombocytosis: Improved microdensitometric measurements with a new image analysis system
Author(s) -
Woods M. J.,
Greaves M.,
Trowbridge E. A.
Publication year - 1990
Publication title -
european journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.904
H-Index - 84
eISSN - 1600-0609
pISSN - 0902-4441
DOI - 10.1111/j.1600-0609.1990.tb00383.x
Subject(s) - thrombocytosis , megakaryocyte , nuclear dna , feulgen stain , pathology , bone marrow , medicine , nuclear medicine , biology , platelet , microbiology and biotechnology , staining , haematopoiesis , genetics , gene , stem cell , mitochondrial dna
Megakaryocyte (MK) nuclear deoxyribonucleic acid (DNA) content was measured on a new image analysis system. Feulgen‐stained bone marrow aspirate smears were analysed from 9 patients with thrombocytosis. Average optical density (OD) of stained nuclei was evaluated by pixel discrimination over 128 grey levels. Projected nuclear area was delineated manually. The product of these two parameters gave an index of nuclear DNA content. Neutrophils were used as 2N reference cells. Reproducibility of OD, nuclear area and their product was excellent for individual cells (CV <2.0% for MKs, <4.0% for neutrophils). The average CV for DNA content of 18 groups of 10 neutrophils was 5.5% (range 3.0–9.7%). A significant linear regression existed between MK nuclear area and DNA content (p < 0.001) for 627 MKs in essential thrombocythaemia (ET) and 346 MKs in reactive thrombocytosis (RT). Compared with RT, more 8N and 64N MKs were seen in ET (p < 0.05). 128N MKs were unique to ET. Image analysis of MK ploidy may assist the clinical discrimination between primary and secondary thrombocytosis.