Browsing by Author "Martinović, Tamara (55178221600)"
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Publication Micromorphological features and interleukin 6, 8, and 18 expressions in post-mortem lung tissue in cases with acute respiratory distress syndrome(2024) ;Kuzmanović, Jelena (53164117100) ;Savić, Slobodan (7005859439) ;Bogdanović, Milenko (57203508508) ;Martinović, Tamara (55178221600) ;Bumbaširević, Vladimir (6603957757)Stevović, Tamara Kravić (55189979900)The purpose of this study was to analyze the presence of interleukins 6, 8, and 18 in post-mortem lung tissue of subjects deceased due to polytrauma. In addition to this, we have described different micromorphological features of lung tissue in ARDS cases associated with fatal traffic trauma. A total of 18 autopsy cases with ARDS after polytrauma and 15 control autopsy cases were analyzed in this study. From every subject, we collected one sample for each lung lobe. All of the histological sections were analyzed by using light microscopy, and for the purpose of ultrastructural analysis, we used transmission electron microscopy. Representative sections were further processed by way of immunohistochemistry analysis. Quantification of IL-6, IL-8, and IL-18-positive cells was conducted by applying the IHC score. We noticed that all samples of ARDS cases exhibited elements of the proliferative phase. Immunohistochemical analysis of lung tissue in patients with ARDS showed strong positive staining for IL-6 (2.8 ± 0.7), IL-8 (2.2 ± 1.3), and IL-18 (2.7 ± 1.2), while staining of the control samples resulted in no positivity to low/moderate positivity (for IL-6 1.4 ± 0.5; for IL-8 0.1 ± 0.4; for IL-18 0.6 ± 0.9). Only IL-6 correlated negatively with the patients’ age (r = −0.6805, p < 0.01). In this study, we described microstructural changes in lung sections of ARDS cases and control cases, as well as interleukins’ expression, demonstrating that autopsy material is as informing as tissue samples collected by performing open lung biopsy. © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2023. - Some of the metrics are blocked by yourconsent settings
Publication Ultrastructural and morphometric analysis of enlarged platelets in congenital isolated asplenia(2019) ;Marković, Olivera (57205699382) ;Martinović, Tamara (55178221600) ;Cirić, Darko (55810852000) ;Trpinac, Dušan (6602163849) ;Martinović, Vesna Čemerikić (21743118200) ;Bumbaširević, Vladimir (6603957757) ;Bila, Jelena (57208312102) ;Marisavljević, Dragomir (55945359700)Kravic-Stevović, Tamara (35275295500)Introduction: Congenital asplenia is an extremely rare condition that can be separate entity due to a specific defect of spleen development or may occur in the context of a malformation syndrome. The patients with asplenia have thrombocytosis and susceptibility to life-threatening infections. Case report: We report a 52-years-old female patient with isolated congenital asplenia with pseudothrombocytopenia and giant platelets. Estimation of platelets life with radioactive indium showed normal lenght of platelets life (9 days). Flow cytometric analysis of platelets showed normal expression of CD41 and CD42b antigens. The mean platelet diameter of asplenic patient measured on the ultrathin sections by the transmission electron microscope was significantly higher than in the healthy individuals (3.81 ± 1.16 μm vs. 2.37 ± 0.61 μm, p < 0.05). There were very few platelets of diameter more than 4 μm found in healthy individuals (around 1%) in comparison to > 40% of the patient's platelets. The ultrastructural studies revealed normal morphology of megakaryocytes. The platelets were uniformly spheroid in shape with conspicuous pseudopodia and the centralization of granules. There were no marginal bands of microtubules inside the platelets. Conclusion: The first case of congenital asplenia with the pseudothrombocytopenia and giant platelets is presented. We discussed the pathogenesis of giant platelets and possible relation of observed ultrastructural changes of platelets with the severe three-vessel coronary artery disease in our patient. © 2019 Inst. Sci. inf., Univ. Defence in Belgrade. All rights reserved.
