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https://www.selleckchem.com/products/gdc-0068.html Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL) is a rare primary and highly aggressive intestinal T-cell lymphoma derived from intraepithelial lymphocytes. MEITL is previously designated as type II enteropathy-associated T cell lymphoma (EATL). Unlike to classic form of EATL, MEITL is not associated with celiac disease. The diagnosis of MEITL is very challenging and the clinical outcome of patients with MEITL is very poor. Herein we describe a series of four patients diagnosed with MEITL identified upon a 10-year institutional retrospective review. Histopathologic examination of these cases revealed monotonous population of medium sized cells infiltrating intestinal mucosa, positive for CD3, CD8 and CD56 in all four cases. Two patients had the combination chemotherapy; however, the average survival time was only 7.5 months for these two patients after diagnosis. The aim of the present case series is to highlight the pathology, diagnosis and clinical course of the patients with MEITL based on the current literature. Dissemination of extended-spectrum beta-lactamase (ESBL) genotypes in gained attention as superbugs, which are extremely difficult to treat with conventional antibiotics. The study aimed to delineate the empirical therapy and the occurrence of SHV, TEM, and CTX-M encoding among pediatric patients. A total number of 33,400 continuous and non-repetitive clinical specimens collected from the debilitated pediatric patients processed for the isolation of . The characterization of the isolated strains performed using phenotypic and molecular methods. The spectrum of antibacterial resistance observed against all the isolated strains of RESULTS A total of 74 (18.8%) ESBL producers isolated, out of which 58 (78.4%) were , 53 (71.6%) , and 38 (51.4%) were genes. The mortality was significantly associated ( <0.001) in patients infected with ESBL producing and neonatal age group. The mean length of st

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