Despite identifying that rheumatic fever (RF) is the result of an immunological reaction following group-A beta-hemolytic streptococcal infection, the pathogenesis remains elusive. RF has been incorrectly designated as causing pancarditis, since it does not cause myocarditis. Research directed toward myocarditis, targeting myosin to unravel the pathogenesis has not succeeded in more than 60 years. RF causes permanent damage to cardiac valves. The mitral valve (MV), derived from the wall of the left ventricle, is composed of a central core of connective tissue, covered on both sides by endothelium. The left ventricle does not have either myocardial or intermyocardial connective tissue involvement in RF. By exclusion, therefore, the primary site of RF damage appears to be the endothelium. Evaluation of the histopathology and immunopathology indicates that RF is a disease of the valvular and vascular endothelium. It is not a connective tissue disorder. Research to identify pathogenesis needs to be focused toward valvular endothelium.
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http://dx.doi.org/10.4103/0974-2069.99621 | DOI Listing |
Purpose: The purpose of this study was to assess the impact of subepithelial connective tissue graft (CTG) on soft tissue volume and aesthetics around implants placed in aesthetically important areas over a 4-year period.
Materials And Methods: A total of 42 participants were divided into groups: implant+CTG (n=20) and implant only (n=22) and evaluated after 48 months using various clinical and radiographic parameters, professional aesthetic assessment, patient-centered aesthetic evaluation, and quality of life improvement measured by OHIP-14 at 12 and 48 months.
Results: Eight patients were lost to follow-up, leaving 34 patients for evaluation.
Indian J Pathol Microbiol
March 2025
Department of Oral and Maxillofacial Pathology and Oral Microbiology, Subharti Dental College and Hospital, Swami Vivekanand Subharti University, Meerut, Uttar Pradesh, India.
Background: Since the introduction, hematoxylin and eosin (H and E) have been a gold standard stain for routine histopathological diagnosis of biopsied specimens. Xylene, despite its hazardous toxic effects, is the most commonly used deparaffinizing agent and forms an imperative part of this staining procedure. In the pursuit to eliminate the use of xylene, various substitutes became available, some with as many if not more hazards.
View Article and Find Full Text PDFA traumatic bone cyst is a pseudocyst, lacking an epithelial lining, and may contain fluid, connective tissue, or both. The pathogenesis of traumatic bone cyst remains unknown, but the most accepted explanation is the traumatic hemorrhagic theory. A traumatic bone cyst typically presents as a radiolucent lesion.
View Article and Find Full Text PDFCOPD
March 2025
Department of Physiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Purpose: Cigarette smoke activates lung inflammation and destruction and the development of COPD. Among various factors influenced by lung inflammation, adiponectin produced by lung epithelial cells is thought to play a significant role in regulating inflammation and maintaining tissue integrity. This study aims to examine adiponectin expression in a mouse model of cigarette smoke extract (CSE)-induced emphysema and explore the effects of adiponectin on cell survival and cytokine gene expression in CSE-induced lung epithelial cell damage.
View Article and Find Full Text PDFFront Endocrinol (Lausanne)
March 2025
Medical Sociology and Psychobiology, University of Potsdam, Potsdam, Germany.
Introduction: Early life stress (ELS) impacts neurotransmitters and cell communication, potentially disrupting neurological and physiological processes. Recently, ELS has been implicated in impaired bone metabolism, with extracellular vesicles (EVs) and their cargo, microRNAs (miRNAs), might affecting this process. This research aimed to elucidate the association between childhood trauma, a specific form of ELS, and bone metabolism through studying miRNA in EVs within three steps: firstly, examining alterations of EV miRNAs between ELS and controls, secondly analyzing associations between altered EV miRNAs and bone markers, and thirdly exploring the target gene prediction and enrichment pathways of altered EV miRNAs.
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