- Auteur(s) : Esteve Darwich, Asunción Vicente, Maria C. Bolling, Maria A. González-Enseñat, Victoria Cusi, Claudia Fortuny, José A. Bombí, Marcel F. Jonkman, José M. Mascaró Jr.
, Department of Dermatology, Department of Pathology,
Hospital Clínic and University School of Medicine, C/ Villarroel 170. CP: 08036 Barcelona, Spain, Department of Dermatology, Department of Pathology, Department of Pediatrics,
Hospital Sant Joan de Déu,
Esplugues de Llobregat, Spain, Department of Dermatology,
University Medical Center Groningen,
- Mots-clés : acantholysis, Dowling Meara, epidermolysis bullosa simplex, histology, newborn, ultrastructural
- Page(s) : 966-71
- DOI : 10.1684/ejd.2011.1497
- Année de parution : 2012
Epidermolysis bullosa (EB) is a heterogeneous group of inherited skin disorders characterized by blistering and skin fragility secondary to mechanical trauma. Epidermolysis bullosa simplex (EBS) is the most frequent form of EB, with Dowling-Meara (DM-EBS) subtype being the most severe form in this group. Conventional histopathological evaluation is usually of low value in the diagnosis of EB, and significant histological features have rarely been reported in this group of diseases. We describe a case of severe DM-EBS in which acantholysis was observed in the histological examination. This finding led us to consider other diagnoses, such as neonatal pemphigus vulgaris or lethal acantholytic EB. Histological, immunological, ultrastructural and genetic tests were performed, leading to a final diagnosis of DM-EBS. Therefore, we believe that DM-EBS should be considered in the differential diagnosis of a newborn with blisters, where acantholysis is the main histological feature.