Chloracne: a case series on cutaneous expression of CYP1A1 as diagnostic biomarker.
Marco Adriano ChessaMichelangelo La PlacaAnnalisa PatriziA VirdiC MiscialiG FedrizziFederica FilippiJ-H SauratO SorgF FontaoG KayaI NeriPublished in: Clinical and experimental dermatology (2021)
Chloracne, also known as metabolizing acquired dioxin-induced skin hamartomas (MADISH), is a rare disfiguring disease related to dioxin exposure. There is a paucity of literature on the clinical manifestations and pathogenesis of chloracne/MADISH. The aim of this study was to assess the clinical features of this very unusual acneiform eruption and to explore the pathogenesis of the disease. This was a retrospective, observational report study was conducted on five patients belonging to the same nuclear family (father, mother and three children) and a relative (father's brother) living in the same house. Histopathological, immunohistochemical, laboratory and toxicological analyses were performed for all patients. The results suggest that CYP1A1 in human skin is a diagnostic biomarker in chloracne, and was positive for all the patients in our sample. Tetrachlorodibenzo-p-dioxin is the most investigated dioxin responsible for chloracne; however, several other agonists, whether dioxin-like or not, can activate the aryl hydrocarbon receptor. To our knowledge, this Italian case series is the first study to suggest polychlorinated biphenyls as a possible cause of an overstimulation of aryl hydrocarbons causing the consequent acneiform eruption.
Keyphrases
- end stage renal disease
- ejection fraction
- chronic kidney disease
- newly diagnosed
- peritoneal dialysis
- healthcare
- prognostic factors
- systematic review
- young adults
- oxidative stress
- patient reported outcomes
- poor prognosis
- patient reported
- long non coding rna
- endothelial cells
- cross sectional
- single molecule
- binding protein