Intrahepatic eosinophilic proliferative pylephlebitis (EPP) in Japanese Black (JB) cattle generally has been considered to be an atypical form of fascioliasis. However, there are many cases of EPP in which no Fasciola spp. have been detected in the livers of affected cattle. The aims of this study were to ascertain the relationship between EPP and hepatic fascioliasis and to investigate the role of food allergy in the disease. Histologically, EPP lesions were characterised by severe endothelial proliferation of the interlobular veins, accompanied by varying degrees of fibrosis and eosinophilic infiltration in portal areas, which could be differentiated from chronic cholangiohepatitis, the typical lesion of hepatic fascioliasis. In addition to hepatic lesions, all cases of EPP had varying degrees of eosinophilic infiltration in the perilymphoid red pulp of the spleen, whereas both affected and unaffected animals had eosinophilic infiltrates in the mucosa of the small intestine. Antibodies against Fasciola spp. were detected in 1/14 EPP cases by ELISA; the seropositive case had EPP in combination with chronic cholangitis. There was no significant difference in total concentration of IgE between cases of EPP and unaffected cattle. Serum IgE levels specific to curly dock (Rumex crispus) and oats (Avena sativa) were higher in EPP cases than in unaffected cattle by allergen profiling screening testing and ELISA. The results of this study suggest that hepatic fascioliasis is unlikely to be the cause of EPP in JB cattle and that food allergens should be investigated as possible aetiological agents.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.tvjl.2012.10.006 | DOI Listing |
Children (Basel)
October 2024
Division of Neonatology, Department of Pediatrics, Faculty of Medicine and University Hospital Cologne, University of Cologne, 50937 Cologne, Germany.
Int Endod J
January 2025
Department of Periodontics & Oral Implantology, PGIDS, Rohtak, India.
Aim: The aim of this study is to compare the outcomes of restricted partial pulpotomy (R-PP) versus extended partial pulpotomy (E-PP) for managing cariously exposed mature permanent molars with symptomatic irreversible pulpitis (SIP).
Methodology: This double-arm, parallel designed randomized clinical trial was registered at clinicaltrials.gov (registration number: NCT05406557).
Diagn Microbiol Infect Dis
December 2024
Microbiology Department, University and Polytechnic Hospital La Fe Valencia, Spain; Severe Infection Research Group, Health Research Institute Hospital La Fe Valencia, Spain.
Background: Invasive pneumococcal disease (IPD) remains a significant concern among children under 5, despite vaccination efforts. This study assessed IPD prevalence and associated risks in pediatric population.
Methods: An observational, retrospective, multicenter study in Comunidad Valenciana, Spain, of IPD cases in children under 13 from January 2012 to September 2022.
Neurol Genet
October 2024
From the Departments of Biomedical Data Science (S.L., J.G.), Epidemiology (S.L., M.N.P.), and Neurology, Geisel School of Medicine at Dartmouth (E.W.S.), Dartmouth College, Hanover; Dartmouth Health (A.S.A., K.M.S., K.A.C., E.W.S.), Lebanon, NH; Neuromuscular Diseases Research Section (B.J.T., A.S., R.C.), National Institute on Aging; National Institute of Neurological Disorders and Stroke (B.J.T.), National Institutes of Health, Bethesda; RNA Therapeutics Laboratory (B.J.T.), National Center for Advancing Translational Sciences, National Institutes of Health, Rockville, MD; Cleveland Clinic (R.M.K.), OH; Department of Medicine (E.P.P.), University of British Columbia, Vancouver, BC, Canada; and University of Miami Miller School of Medicine (W.G.B.), FL.
Front Pediatr
August 2024
Pediatric Endocrinology Unit, Pediatric Department, Irmandade da Santa Casa de Misericórdia de São Paulo and Santa Casa de Sao Paulo School of Medical Sciences, São Paulo, Brazil.
Introduction: Ectopic posterior pituitary (EPP) is a rare congenital abnormality, sometimes associated with other midline defects, such as pituitary stalk interruption syndrome (PSIS), in which thin or absent pituitary stalk and anterior pituitary hypoplasia are combined to EPP. Most cases are sporadic, with few reports of familial cases, and many congenital hypopituitarism (CH) cases remain unsolved.
Objective: To search for candidate genes associated with this condition, we performed trio-based whole-exome sequencing (WES) on patients with EPP, including two familial cases.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!