Search results for "Severe course"

showing 2 items of 2 documents

Association of elevated serum triglyceride levels with a more severe course of acute pancreatitis: Cohort analysis of 1457 patients.

2019

Previous publications have reported an association between hypertriglyceridemia (HTG) and severity of acute pancreatitis, but this relationship remains somewhat controversial.To evaluate the outcome of acute pancreatitis according to serum triglyceride levels on admission.Retrospective analysis of prospectively collected data, which included all consecutive cases of acute pancreatitis admitted to a tertiary hospital (January 2002-December 2014). Acute pancreatitis patients were classified into 3 groups based on serum triglyceride levels (mg/dl) measured within 48 h from admission: normal triglycerides-mild HTG (200); moderate HTG (200-749); severe HTG (≥750). Primary outcomes were the diffe…

AdultMalemedicine.medical_specialtyMultivariate analysisNecrosisAdolescentEndocrinology Diabetes and MetabolismMultiple Organ FailureGastroenterologyCohort Studies03 medical and health scienceschemistry.chemical_compoundYoung Adult0302 clinical medicineRisk FactorsInternal medicinemedicineHumansPancreasTriglyceridesAgedRetrospective StudiesAged 80 and overHypertriglyceridemiaHepatologyTriglyceridebusiness.industryPancreatitis Acute NecrotizingHypertriglyceridemiaGastroenterologyMiddle Agedmedicine.diseasePrognosisTreatment OutcomechemistryPancreatitis030220 oncology & carcinogenesisAcute DiseaseAcute pancreatitisPancreatitis030211 gastroenterology & hepatologyFemalemedicine.symptomSevere coursebusinessCohort studyPancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]
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Recurrent Granular Dystrophy of the Cornea

2006

Purpose: To describe a case of severe corneal granular dystrophy with clinicopathologic and molecular genetic findings. Methods: The DNAs of a 53-year-old male patient suffering from corneal granular dystrophy and nonaffected family members was analyzed by molecular genetic methods. Clinical features, and histopathologic and immunohistochemical findings from the penetrating keratoplasty specimen, are described. Results: Histopathologic and molecular genetic findings confirmed the diagnosis. A new genetic polymorphism is described. Histopathologic evidence supports the assumption of the epithelial origin of the described dystrophy. Conclusions: A severe course of corneal granular dystrophy c…

MalePathologymedicine.medical_specialtymedicine.medical_treatmentDNA Mutational AnalysisBiologyPolymerase Chain ReactionPhototherapeutic keratectomyRecurrenceTransforming Growth Factor betaCorneamedicineHumansMutational statusMolecular BiologyCorneal Dystrophies HereditaryExtracellular Matrix ProteinsPolymorphism GeneticUnusual caseDystrophyExonsMiddle AgedOphthalmologymedicine.anatomical_structureMutationImmunohistochemistrySevere courseNovel mutationKeratoplasty PenetratingCornea
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