European Journal of Dermatology · 2019 · 13 citations · 7 references
MedicinePediatricsPediatric Head SurgeryCongenital Neck AnomaliesLymphatic MalformationsCongenital Cervical LymphangiomaLymphatic Malformation SclerotherapyNeck Lymphatic Malformations
Background: The significance of individual risk factors in the development of contact allergy, such as genetic variation in cytokine genes and atopy, is still not clearly defined. Objectives: The aim of this study was to investigate the association between TNFα 308G>A polymorphism or atopy and contact sensitization (CS) in a cohort from the general Croatian population. Materials & Methods: The study involved 312 first-year students from the University of Zagreb (median age: 19 years). Methods included a questionnaire and skin prick and patch testing for common inhalable and contact allergens, respectively, as well as genotyping for TNFα 308G>A polymorphism based on buccal swabs. Results: CS (positive patch test for ≥1 contact allergen) was reported in 32%, atopy (positive prick test for ≥1 inhalable allergen) in 38%, and TNFα 308G>A polymorphism in 23% of subjects. Based on multivariate analysis, atopy was confirmed as a predictor of CS, poly-sensitization, CS to p-phenylenediamine and cobalt chloride, and self-reported skin symptoms. TNFα 308G>A polymorphism was confirmed as a predictor of CS to p-phenylenediamine (OR: 5.72; 95% CI 1.20-27.28). Conclusion: These findings could be relevant for evaluation of individual susceptibility to developing a contact allergy, particularly among persons occupationally exposed to skin hazards.
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The EXIT procedure: Experience and outcome in 31 cases
Sarah Bouchard, Mark P. Johnson, Alan W. Flake et al. · Journal of Pediatric Surgery · 2002 · 372 citations