Epidermolysis bullosa acquisita mediated by IgA immunoglobulins of childhood
Journal Title: Dermatologia Kliniczna - Year 2008, Vol 10, Issue 2
Abstract
We present an 11 -years-old girl with disseminated tense blisters on the face and abdomen accompanied by erosions on oral mucosa. Based on the clinical features and results of immunofluorescence study on patient’s skin diagnosis of linear IgA bullous dermatosis (LABD) was established. During 7 months the patient was treated with combined therapy using dapsone and metylprednisolone with remissions and relapses. This time skin lesion were limited to the traumatized areas and healing with atrophic scars and milia. Taking under consideration changing clinical picture laser scanning confocal microscopy (LSCM) was performed showing the presence of in vivo bound immunoglobulions below the collagen IV, characteristically for epidermolysis bullosa ac-quisita (EBA). Indirect immunofluorescence study disclosed the presence of circulating IgA antibody at the basement membrane zone. Our study showed that inflammatory type of EBA of childchood may mimic LABD and an application of LSCM allows differentiating EBA from LABD.
Authors and Affiliations
Małgorzata Huczek, Katarzyna Woźniak
Fluorescence patterns in indirect immunofluorescence on HEp-2 cells and antigens recognized in blot test in patients supposed to have a connective tissue disease
Introduction: Connective tissue diseases (CTD) are caused by interplay between genetic and environmental factors. Autoantibodies against diverse nuclear antigens (ANA) play an important role in their pathogenesis. Patien...
Preliminary evaluation of selected psychological parameters in patients with acne
Introduction: Acne vulgaris is the most common skin disease. This chronic skin disorder induces negative psychological and social effects such as anxiety, depression and a reduction in social functioning. Consequenc...
Przypadek obrzęku przedgoleniowego – trudności w diagnostyce i leczeniu
Obrzęk przedgoleniowy (oedema pretibiale) występuje u niektórych chorych na chorobę Gravesa-Basedowa. Pojawia się szczególnie rzadko u chorych, którzy mają oftalmopatię lub akropachię tarczycową. Przedstawiono przypadek...
Nietypowy przypadek liszaja śluzowatego twardzi nowego towarzyszącego chorobie tarczycy
Liszaj śluzowaty twardzinowy (scleromyxedema), zespół Arndta-Gottrona, jest schorzeniem należącym do dużej grupy skórnych mucynoz. Przedstawiono przypadek liszaja śluzowatego twardzinowego związanego z chorobą tarczycy (...
An assessment of expectations of patients with stasis ulcers of lower extremities, remaining underthe care of family physicians, according to their family members and/or caretakers and the realization of treatment goals
Introduction: Stasis ulcers of lower extremities represent a serious health problem in a daily practice of family physicians. In order to get a better understanding of the needs of patients' with stasis ulcers of lower e...