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Background: (), a significant pathogen in gastrointestinal diseases, has been implicated in various oral pathologies. Accurate detection of in oral biopsies is crucial for understanding its role in oral diseases.
Materials And Methods: A total of 100 oral biopsy samples were collected from patients presenting with suspected oral lesions. The samples were subjected to Giemsa staining and immunohistochemistry (IHC) using anti- antibodies. The sensitivity, specificity, and diagnostic accuracy of Giemsa staining were assessed using IHC as the gold standard. Arbitrary values: Giemsa-positive cases were observed in 65% of samples, while IHC detected in 70%. Statistical analysis was conducted using Chi-square tests and kappa agreement.
Results: Giemsa staining exhibited a sensitivity of 85%, specificity of 90%, and an overall diagnostic accuracy of 88% when compared to IHC. There was substantial agreement (kappa = 0.76) between the two methods. While Giemsa staining was less expensive and quicker, IHC provided greater specificity, particularly in cases with low bacterial density.
Conclusion: Giemsa staining is a reliable, cost-effective method for detecting in oral biopsy specimens. However, IHC remains the gold standard due to its higher specificity and ability to detect low-density infections. Combining both techniques may enhance diagnostic accuracy in clinical settings.
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http://dx.doi.org/10.4103/jpbs.jpbs_127_25 | DOI Listing |
Background: The white cell precursor (WPC) channel of the Sysmex XN-series hematology analyzer, which is designed for blast detection, showed reduced sensitivity for blast detection in leukopenic patients undergoing chemotherapy. This study aimed to evaluate the gating region for apoptotic blasts in the WPC scattergram to enhance detection sensitivity.
Methods: NOMO-1 cells, a human acute monoblastic leukemia cell line, were treated with varying concentrations of cytarabine (0, 100, 500, and 1,000 nM) for three days to induce apoptosis.
Turkiye Parazitol Derg
September 2025
Ege University Faculty of Medicine, Department of Parasitology, İzmir, Türkiye.
Objective: Leishmaniasis, caused by protozoan parasites of the spp., presents significant global health challenges, with visceral leishmaniasis (VL) and cutaneous leishmaniasis forms causing severe morbidity and mortality. Macrophages serve as primary host cells, where spp.
View Article and Find Full Text PDFJ Ethnopharmacol
September 2025
P. G. Department of Biosciences, Sardar Patel University, Satellite Campus, Bakrol, Gujarat, India. Electronic address:
Ethnopharmacological Relevance: Carissa carandas L. ('Karonda'), a medicinal shrub from the Apocynaceae family, has been traditionally used in Indian ethnomedicine for the treatment of inflammation, infections, and respiratory disorders. Its phytochemically rich extracts have demonstrated diverse pharmacological activities, including antioxidant, anti-inflammatory, antimicrobial, hepatoprotective, and anticancer effects.
View Article and Find Full Text PDFJ Ethnopharmacol
September 2025
Laboratório de Parasitos e Vetores, Departamento de Ciências Farmacêuticas, Instituto de Ciências Biológicas e da Saúde, Universidade Federal Rural do Rio de Janeiro, Seropédica - RJ, Brazil. Electronic address:
Ethnopharmacological Relevance: Schinus genus plants have a long history of use in traditional medicine, particularly in South America. The ethnopharmacological applications of Schinus species include antiseptic, antiplasmodial, antimalarial and antileishmanial properties.
Aim Of The Study: In the present work, we investigated the action of essential oil (EO) against cutaneous leishmaniasis causing agent Leishmania amazonensis in promastigote and amastigote forms as well as cytotoxicity against host cells.
J Biochem Mol Toxicol
September 2025
Department of Molecular Biology and Genetics, Institute of Natural and Applied Sciences, Van Yüzüncü Yıl University, Van, Türkiye.
The objective of this study was to examine the chemotherapeutic effect of CAPE, via the mitochondrial membrane potential (MMP, Δψm) pathway in TPC-1 human papillary thyroid cancer cells. The cytotoxic effect of CAPE was evaluated using MTT and crystal violet assays, while its apoptotic activity was measured using Bax, Bcl-2, Caspase-3,-8,-9 and Apaf-1 assays. Effects on mitochondria were performed by analyzing JC-1 fluorescent probe-MMP, ROMO1 and mitochondrial ATP-synthase.
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