Assessment of cell proliferation by Ki-67 staining and flow cytometry in fine needle aspirates (FNAs) of reactive lymphadenitis and non-Hodgkin's lymphomas

Citation
F. Schmitt et al., Assessment of cell proliferation by Ki-67 staining and flow cytometry in fine needle aspirates (FNAs) of reactive lymphadenitis and non-Hodgkin's lymphomas, CYTOPATHOLO, 10(2), 1999, pp. 87-96
Citations number
24
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology
Journal title
CYTOPATHOLOGY
ISSN journal
09565507 → ACNP
Volume
10
Issue
2
Year of publication
1999
Pages
87 - 96
Database
ISI
SICI code
0956-5507(199904)10:2<87:AOCPBK>2.0.ZU;2-W
Abstract
This study was undertaken to assess cell proliferation in FNAs from a serie s of 57 non-Hodgkin's lymphomas (NHL) and 11 cases of reactive lymphadeniti s using Ki-67 staining and flow cytometry (FCM). The results were compared and correlated to the cytomorphological subgrouping according to Kiel class ification. The mean percentages of Ki-67 positivity were 16.6% and 61.1% fo r low and high grade lymphomas, respectively (P < 0.001). The mean S-phase fraction (SPF) determined by FCM was 4.6% for low grade and 12.9% for high grade lymphomas (P < 0.001). The figures for Ki-67 positivity and S-phase f raction in reactive lymphadenitis were 16.8% and 4%, respectively. We obser ved a strong correlation in low grade lymphomas between Ki-67 and SPF. A go od correlation was also found in reactive lymphadenitis. In high grade lymp homas, however, with highly scattered Ki-67 and S-phase values, this correl ation was lost. In some cases this discrepancy can be explained by a rich a dmixture of non-neoplastic, non-proliferating cells in aspirates from diplo id rumours. In addition, the existence of a minor aneuploid tumour cell pop ulation of high proliferation such as that in Ki-l lymphomas will not be ac curately analysed by FCM but is easily assessed by Ki-67 staining. However, the main reason seems to be a high variability between the Fraction of cel ls in S-phase and the total number of cells in G(1), S and G(2) in individu al tumours.