13 research outputs found

    Heterotopic gastrointestinal cyst mimicking chronic cholecystitis: a case report

    Get PDF
    <p>Abstract</p> <p>Introduction</p> <p>Heterotopic gastric mucosa is described almost everywhere in the gastrointestinal tract, from the oral cavity to the rectum. The occurrence of heterotopic gastric tissue in the gallbladder is rare. A choristoma can be defined as a new growth developing from a displaced anlage not normally present in the anatomical site where it developed. We present an extremely uncommon case of a cyst (choristoma) attached to the gallbladder, which contained gastric and intestinal mucosa.</p> <p>Case presentation</p> <p>A 33-year-old woman was hospitalized with clinical symptoms of chronic cholecystitis. The laboratory findings were within the normal range. Abdominal ultrasonography revealed a thickened gallbladder wall and a stone in the cystic duct was suspected. In the course of laparoscopic cholecystectomy, a cyst was visualized in the vicinity of the duct and the gallbladder neck. Microscopic examination of the removed cyst revealed evidence of gastric, duodenal and small-intestinal mucosa. The immunohistochemical study revealed many endocrine cells, which were positive for several endocrine cell markers such as chromogranin, serotonin, gastrin and so on. It can be inferred that the observed cyst had arisen from the foregut early in the development of the gastrointestinal tract.</p> <p>Conclusion</p> <p>The presence of endocrine cells together with epithelial cells supports the hypothesis that these had developed simultaneously, and that the endocrine cells had probably supported the development of the epithelial cells by the release of hormones and growth factors. To the best of the authors' knowledge, this report is the first to report a gastrointestinal cyst choristoma with endocrine cells in the region of the cystic duct and gallbladder.</p

    Design and baseline characteristics of the finerenone in reducing cardiovascular mortality and morbidity in diabetic kidney disease trial

    Get PDF
    Background: Among people with diabetes, those with kidney disease have exceptionally high rates of cardiovascular (CV) morbidity and mortality and progression of their underlying kidney disease. Finerenone is a novel, nonsteroidal, selective mineralocorticoid receptor antagonist that has shown to reduce albuminuria in type 2 diabetes (T2D) patients with chronic kidney disease (CKD) while revealing only a low risk of hyperkalemia. However, the effect of finerenone on CV and renal outcomes has not yet been investigated in long-term trials. Patients and Methods: The Finerenone in Reducing CV Mortality and Morbidity in Diabetic Kidney Disease (FIGARO-DKD) trial aims to assess the efficacy and safety of finerenone compared to placebo at reducing clinically important CV and renal outcomes in T2D patients with CKD. FIGARO-DKD is a randomized, double-blind, placebo-controlled, parallel-group, event-driven trial running in 47 countries with an expected duration of approximately 6 years. FIGARO-DKD randomized 7,437 patients with an estimated glomerular filtration rate >= 25 mL/min/1.73 m(2) and albuminuria (urinary albumin-to-creatinine ratio >= 30 to <= 5,000 mg/g). The study has at least 90% power to detect a 20% reduction in the risk of the primary outcome (overall two-sided significance level alpha = 0.05), the composite of time to first occurrence of CV death, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for heart failure. Conclusions: FIGARO-DKD will determine whether an optimally treated cohort of T2D patients with CKD at high risk of CV and renal events will experience cardiorenal benefits with the addition of finerenone to their treatment regimen. Trial Registration: EudraCT number: 2015-000950-39; ClinicalTrials.gov identifier: NCT02545049

    Procedure-Type Risk Categories for Pediatric and Congenital Cardiac Catheterization

    No full text

    Optimal number of routing paths in multi-path routing to minimize energy consumption in wireless sensor networks

    Get PDF
    In wireless sensor networks, multi-path routing is proposed for energy balancing which prolongs the network lifetime as compared to single-path routing where utilization of a single route between a source node and the base station results in imbalanced energy dissipation. While it is evident that increasing the number of routing paths mitigates the problem of energy over-utilization in a subset of nodes acting as relays, the net effect of the proliferation of multiple routing paths on energy balancing remains unclear. It is imperative to keep the number of routing paths as low as possible without significantly deteriorating the network lifetime; therefore, determination of the optimal number of routing paths in multi-path routing by considering the tradeoff in routing complexity and network lifetime extension is an interesting research problem. In this study, to investigate the impact of the number of routing paths in multi-path routing on network-wide energy balancing under optimal operating conditions, we build a novel mixed integer programming framework. We explore the parameter space consisting of a number of paths, number of nodes, maximum transmission range, network area, and network topology. The results of the analysis show that by utilizing the optimization scheme proposed, it is possible to achieve near-optimal energy consumption (within 1.0% neighborhood of the case where no restrictions are imposed on the number of routing paths in multi-path routing) using at most two paths for each node.Publisher's Versio
    corecore