lewis-x-antigen and Coronary-Thrombosis

lewis-x-antigen has been researched along with Coronary-Thrombosis* in 2 studies

Other Studies

2 other study(ies) available for lewis-x-antigen and Coronary-Thrombosis

ArticleYear
Cellularity and structure of fresh human coronary thrombectomy specimens; presence of cells with markers of progenitor cells.
    Journal of cellular and molecular medicine, 2012, Volume: 16, Issue:12

    Acute coronary syndromes and acute myocardial infarctions are often related to plaque rupture and the formation of thrombi at the site of the rupture. We examined fresh coronary thrombectomy specimens from patients with acute coronary syndromes and assessed their structure and cellularity. The thrombectomy specimens consisted of platelets, erythrocytes and inflammatory cells. Several specimens contained multiple cholesterol crystals. Culture of thrombectomy specimens yielded cells growing in various patterns depending on the culture medium used. Culture in serum-free stem cell enrichment medium yielded cells with features of endothelial progenitor cells which survived in culture for a year. Immunohistochemical analysis of the thrombi revealed cells positive for CD34, cells positive for CD15 and cells positive for desmin in situ, whereas cultured cell from thrombi was desmin positive but pancytokeratin negative. Cells cultured in endothelial cell medium were von Willebrand factor positive. The content of coronary thrombectomy specimens is heterogeneous and consists of blood cells but also possibly cells from the vascular wall and cholesterol crystals. The culture of cells contained in the specimens yielded multiplying cells, some of which demonstrated features of haematopoietic progenitor cells and which differentiated into various cell-types.

    Topics: Acute Coronary Syndrome; Antigens, CD34; Biomarkers; Cells, Cultured; Coronary Disease; Coronary Thrombosis; Desmin; Endothelial Cells; Humans; Lewis X Antigen; Myocardial Infarction; Plaque, Atherosclerotic; Stem Cells; Thrombectomy; von Willebrand Factor

2012
Frequency of acute asymptomatic myocardial infarction and an estimate of infarct age in cases of abrupt sudden death observed in a forensic autopsy material.
    Journal of cellular and molecular medicine, 2008, Volume: 12, Issue:5B

    The aim of this study is to determine the frequency of acute infarcts at autopsy in cases of unexpected abrupt deaths in persons with coronary heart disease. In addition, we want to estimate the time between onset of infarct and death based on evolving tissue changes in the infarct known to occur during the first hours. Thirty cases of unexpected, abrupt deaths were selected from a forensic autopsy material. Half of them had a preliminary diagnosis of coronary heart disease, the other half a preliminary diagnosis not involving the heart or chest area. Complete autopsies were performed. The myocardium and the coronary arteries were sampled and examined without knowledge of the gross findings or to which group the case belonged. Myocardial infarcts and acute coronary changes were found in both groups, less frequently in the non-coronary group. The age of the myocardial and coronary lesions was estimated by observing morphological characteristics changing with time, e.g. increasing polymorphonuclear leucocytes in the infarcted myocardium, and increasing amount of fibrin in thrombi. The majority of cases in the coronary group died with an extensive asymptomatic myocardial infarction, which probably had lasted 5-6 hrs or less. Acute changes in the right coronary artery and its area of supply prevailed. Acute myocardial infarcts were observed also in a minority of the non-coronary group, but myocardial infarction was not the cause of death in any of them. Abrupt coronary death is most often preceded by an extensive asymptomatic myocardial infarction within the last 5-6 hrs.

    Topics: Adult; Aged; Autopsy; Complement C9; Coronary Thrombosis; Coronary Vessels; Death, Sudden, Cardiac; Female; Forensic Pathology; Humans; Immunohistochemistry; Lewis X Antigen; Male; Middle Aged; Myocardial Infarction; Myocardium; Organ Size

2008