The utilization of the large unstained cell (LUC) parameter in lymphoid, haematopoietic and related tissue's malignant neoplasms

dc.contributor.authorGök, Gamze
dc.contributor.authorErdoğan, Serpil
dc.contributor.authorAsutay, Erbay
dc.contributor.authorYılmaz, Gülsen
dc.contributor.authorErel, Özcan
dc.contributor.authorYılmaz, Fatma Meriç
dc.date.accessioned2025-10-19T16:20:22Z
dc.date.created2025
dc.date.issued2025
dc.departmentBartın Üniversitesi
dc.description.abstractObjectives: Large unstained cells (LUCs) are a differential count parameter reported by routine hematology analysis, and LUC percentages (LUC%) reflect active lymphocytes and peroxidase-negative cells. We aimed the evaluate the LUC% parameter in routine practice towards malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic, and related tissue. Methods: LUC analysis was performed with Siemens ADVIA® 2120 Hematology System. Data were obtained from Ankara Bilkent City Hospital’s laboratory information system. Results: A statistical difference in the LUC % data in the case of LUC % <4.5 and LUC % ?4.5 among preliminary diagnoses was observed (P<0.001). According to the Kruskal-Wallis test, a statistical difference was observed between preliminary diagnosis and LUC % values (P<0.001). The One-way ANOVA test with Bonferroni correction was performed for post hoc multiple comparisons of the preliminary diagnosis among LUC%. LUC% was higher in Hodgkin Lymphoma patients than Myeloid leukaemia patients (P=0.002). LUC % was higher in the Lymphoid leukaemia patients than in the patients with Hodgkin lymphoma (P<0.001), Other and unspecified types of non-Hodgkin lymphoma (P<0.001), Multiple myeloma and malignant plasma cell neoplasms (P<0.001). LUC% was higher in patients with leukemia unspecified cell type than Hodgkin lymphoma (P<0.001), Follicular lymphoma (P<0.001), Non-follicular lymphoma (P<0.001), Mature T-Cell and Natural Killer Cell lymphomas (P<0.001), Other and unspecified types of non-Hodgkin lymphoma (P<0.001), Malignant immunoproliferative diseases (P<0.001), Multiple myeloma and malignant plasma cell neoplasms (P<0.001), Lymphoid leukaemia (P<0.001), Myeloid leukaemia (P<0.001), Other leukaemias of specified cell type patients (P<0.001). Conclusions: The present study underscores the importance of LUC% in line with ICD-10 and may provide ideas for new research. Prospective studies including patient and control groups may be useful in assessing LUC%.
dc.identifier.doi10.18621/eurj.1625710
dc.identifier.endpage740
dc.identifier.issn2149-3189
dc.identifier.issue4
dc.identifier.startpage732
dc.identifier.urihttps://doi.org/10.18621/eurj.1625710
dc.identifier.urihttps://hdl.handle.net/11772/25414
dc.identifier.volume11
dc.language.isoen
dc.publisherPrusa Medikal Yayıncılık
dc.relation.ispartofThe European Research Journal
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzDergiPark_20251017
dc.subjectClinical Oncology
dc.subjectKlinik Onkoloji
dc.subjectHaematological Tumours
dc.subjectHematolojik Tümörler
dc.subjectCancer Diagnosis
dc.subjectKanser Tanısı
dc.titleThe utilization of the large unstained cell (LUC) parameter in lymphoid, haematopoietic and related tissue's malignant neoplasms
dc.typeArticle
dspace.entity.typePublication

Dosyalar