Prognostic factors for recurrence and survival after resection were analyzed.\n\nResults: A total of 235 patients were included. With a median follow-up of 50.2 (0.07-125.1) months, the recurrence rate was 57.0%. The 1-, 3-, and 5-year overall survival rates were 83.9%, 66.0%, and 58.1% respectively. Multivariate analysis demonstrated that multi-focal lesions (HR: 2.93, PFTα cell line P < 0.001), alpha-fetoprotein (AFP) level greater than 100 ng/ml (HR: 1.74, P = 0.002) and history of
tumor rupture (HR: 2.84, P = 0.003) were independent risk factors for recurrence of HCC after hepatectomy.\n\nConclusions: Predictors for HCC recurrence can be identified before operation. These important parameters should be considered before and after contemplating curative resection for HCC patients and for risk stratification in future AZD1208 clinical trials for neoadjuvant or post-resection adjuvant therapy. The possible use of neoadjuvant or adjuvant treatment
to improve survival should be addressed by further trials. Crown Copyright (c) 2011 Royal College of Surgeons of Edinburgh (Scottish charity number SC005317) and Royal College of Surgeons in Ireland. Published by Elsevier Ltd. All rights reserved.”
“Background: The pleuropneumonia caused by Actinobacillus pleuropneumoniae is one the most important swine respiratory diseases. Biochemical and serological tests are widely applied for the diagnosis and characterization of this bacterium. However, in some isolates, conflicting results are found. There are at least 15 serotypes with significant differences in virulence that have been identified until now. Moreover, cross reactions between serotypes are not uncommon. The serotype determination from isolates occurring in outbreaks is an important procedure in prophylaxis and control of the disease. The present work focuses on the application of an ERIC-PCR technique for genotyping and differentiation of A. pleuropneumoniae isolates.\n\nMaterials, Methods & Results: Fifteen reference strains for the recognized A. pleuropneumoniae serotypes were analyzed in this work, alongside with 27 field isolates that had been previously characterized regarding
biochemical, serological and molecular features. Total DNA from each sample was purified and subjected to PCR amplification using Lazertinib price ERIC-specific primers (ERIC1R and ERIC2). The resulting amplicons were analyzed by agarose gel electrophoresis and their sizes were estimated from the gel images. Bands with similar sizes were identified and used to construct a binary matrix that took into account the presence or absence of individual bands in all lanes. Pair-wise similarity coefficients were computed from the binary matrix and the similarity matrices obtained were utilized to construct an UPGMA-based dendrogram. The amplicons obtained from the A. pleuropneumoniae reference strains generated a very distinctive pattern for each one of the tested strains.