Flow Cytometry as an Adjunct to Fine Needle Aspiration Cytology in the Diagnosis and Subtyping of Non-Hodgkin Lymphoma.
[INTRODUCTION] Fine needle aspiration cytology (FNAC) is widely used in the investigation of lymphadenopathy.
APA
Kushwaha P, Jain SL, et al. (2026). Flow Cytometry as an Adjunct to Fine Needle Aspiration Cytology in the Diagnosis and Subtyping of Non-Hodgkin Lymphoma.. Cytopathology : official journal of the British Society for Clinical Cytology, 37(2), 130-139. https://doi.org/10.1111/cyt.70046
MLA
Kushwaha P, et al.. "Flow Cytometry as an Adjunct to Fine Needle Aspiration Cytology in the Diagnosis and Subtyping of Non-Hodgkin Lymphoma.." Cytopathology : official journal of the British Society for Clinical Cytology, vol. 37, no. 2, 2026, pp. 130-139.
PMID
41446962
Abstract
[INTRODUCTION] Fine needle aspiration cytology (FNAC) is widely used in the investigation of lymphadenopathy. FNAC in conjunction with flow cytometry (FCM) immunophenotyping has proven to be a fundamental tool in the diagnosis and subtyping of non-Hodgkin lymphoma (NHL). FCM is objective and offers multiparametric quantitative results and is very useful in assessing the clonality.
[AIM] To evaluate the diagnostic efficiencyof FNAC-FCM immunophenotyping in the definite diagnosis and classification of non-Hodgkin lymphoma.
[MATERIAL AND METHOD] This study retro-prospectively assessed 119 suspected cases of NHL which were diagnosed using FNAC-FCM. The FNAC-FCM diagnoses were correlated with the respective histopathology diagnoses (HPE) and sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) were calculated.
[RESULT] Of the 119 cases, FNAC/FCM provided a definite diagnosis of NHL in 89 cases and 15 cases were reported as "highly suggestive of NHL" (sNHL). 11 cases were reported as reactive lymphoid hyperplasia and 4 as lymphocytic thyroiditis. HPE was available in 48/89 cases of NHL, 13/15 of sNHL and 6/11 cases of reactive lymphoid hyperplasia (RLH). The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were found as follows: 78.6%, 100%, 100% and 31.5% respectively.
[CONCLUSION] The combination of FNAC-FCM is effective in the cytological diagnosis and classification of NHL and generates reproducible results the majority of the time. However, interpretation of FCM should be performed by a trained cytopathologist only because the graphs ought to be assessed in the light of morphology.
[AIM] To evaluate the diagnostic efficiencyof FNAC-FCM immunophenotyping in the definite diagnosis and classification of non-Hodgkin lymphoma.
[MATERIAL AND METHOD] This study retro-prospectively assessed 119 suspected cases of NHL which were diagnosed using FNAC-FCM. The FNAC-FCM diagnoses were correlated with the respective histopathology diagnoses (HPE) and sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) were calculated.
[RESULT] Of the 119 cases, FNAC/FCM provided a definite diagnosis of NHL in 89 cases and 15 cases were reported as "highly suggestive of NHL" (sNHL). 11 cases were reported as reactive lymphoid hyperplasia and 4 as lymphocytic thyroiditis. HPE was available in 48/89 cases of NHL, 13/15 of sNHL and 6/11 cases of reactive lymphoid hyperplasia (RLH). The sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were found as follows: 78.6%, 100%, 100% and 31.5% respectively.
[CONCLUSION] The combination of FNAC-FCM is effective in the cytological diagnosis and classification of NHL and generates reproducible results the majority of the time. However, interpretation of FCM should be performed by a trained cytopathologist only because the graphs ought to be assessed in the light of morphology.
MeSH Terms
Humans; Lymphoma, Non-Hodgkin; Biopsy, Fine-Needle; Flow Cytometry; Female; Male; Middle Aged; Aged; Adult; Immunophenotyping; Cytodiagnosis; Aged, 80 and over; Sensitivity and Specificity; Adolescent