Epidermolysis bullosa in the medical practice of a general practitioner: a study of two cases

Abstract

Dystrophic epidermolysis bullosa is an inherited disease presenting with blistering of the skin and mucous membranes. The authors reviewed a case of siblings suffering from the disease. The first symptoms were noticed at the time of birth, and epidermolysis bullosa was suspected. The lesions appear spontaneously or as a result of a trauma, even during everyday activities connected with getting dressed or hygiene. As well as skin lesions they also have symptoms from other organs, which is a challenge for the primary care paediatrician. Children also need the constant care of specialised team of doctors. The disease is a considerable burden on the life of the whole family; therefore, social support and psychological care are also necessary.

Care problems of a newborn with epidermolysis bullosa – a case study

“…Terapia polega na leczeniu objawowym, przede wszystkim zmian skórnych oraz współistniejących objawów. Ważnymi problemami w momencie planowania działań pielęgniarskich (poza pęcherzami i ranami) są ból, uporczywy świąd i kruchość naskórka oraz nawrotowe nadkażenia skóry [9].…”