Results 51 to 60 of about 6,469 (196)
ABSTRACT Objectives Direct immunofluorescence (DIF) is the gold standard for diagnosing subepidermal blistering diseases (SBDs). However, DIF requires specialized expertise; therefore, alternative immunological methods such as enzyme‐linked immunosorbent assays (ELISA) are worth exploring. The aim of this review was to evaluate the diagnostic agreement
Romeo Patini +9 more
wiley +1 more source
Dermatitis herpetiformis – diagnostic difficulties based on the presentation of own cases
Introduction . Dermatitis herpetiformis (Duhring disease) is an autoimmune blistering subepidermal dermatosis characterized by pruritic polymorphic skin eruption accompanied by a clinically asymptomatic gluten-sensitive enteropathy.
Katarzyna Łoza +4 more
doaj +1 more source
Mycoplasma pneumoniae‐Induced Rash and Mucositis: Clinicopathologic Characterization of 11 Cases
ABSTRACT Background Mycoplasma pneumoniae ‐induced rash and mucositis (MIRM) is a mucocutaneous eruption affecting children and young adults with respiratory tract or clinically occult infection by M. pneumoniae . Mucosal involvement is often robust and may raise concern for Stevens–Johnson syndrome/toxic epidermal necrolysis (SJS/TEN). Histopathologic
Margaret Lang Houser +5 more
wiley +1 more source
THE MANAGEMENT OF DERMATITIS HERPETIFORMIS BY THE GASTROENTEROLOGIST. A SERIES OF CASES
BACKGROUND: Dermatitis herpetiformis (DH) is considered a skin celiac disease (CD). The individuals can be seen by primary care professionals or by dermatologists that could refer the patient to a gastroenterologist.
Lorete Maria da Silva KOTZE +3 more
doaj +1 more source
Navigating the Complexities of Pemphigus Vulgaris: A Comprehensive Iranian Study
We conducted a cross‐sectional analysis of 63 patients diagnosed with pemphigus vulgaris, confirmed by biopsy. Information was collected via telephone interviews. The research aimed to assess the demographic characteristics, initial symptoms, diagnosis delays, and treatment outcomes of the participants.
Delaram Moosavi +7 more
wiley +1 more source
A Rare Type of Bullous Disorder in a Child. Can It Be Chronic Bullous Disease of Childhood?
ABSTRACT Chronic bullous disease of childhood (CBDC), also known as childhood linear IgA bullous dermatosis, is a rare autoimmune disorder characterized by sub‐epidermal blistering and linear deposition of immunoglobulin A at the demo‐epidermal junction.
Rajeev Yadav +3 more
wiley +1 more source
Spesolimab for treatment of generalized pustular psoriasis of pregnancy
Abstract Introduction Generalized pustular psoriasis (GPP) is a severe, desquamating skin disorder associated with pregnancy that presents as fever, fatigue, malaise and sterile pustules. It is associated with profound maternal morbidity, maternal mortality, placental insufficiency and stillbirth.
Jason Bunn +9 more
wiley +1 more source
According to our experience, dermatitis herpetiformis usually occurs in young males who present with an itchy polymorphic eruption, without blisters or even overt vesicles, localized symmetrically on elbows, 1/3 of the proximal part of extensor surfaces ...
Magdalena Jałowska +7 more
doaj +1 more source
ABSTRACT Background Desquamative gingivitis is a clinical condition characterized by erythema, blisters, and erosions within the gingiva. It may be a manifestation of oral lichen planus or autoimmune bullous diseases, such as pemphigus vulgaris and mucous membrane pemphigoid. The identification of the cause of desquamative gingivitis typically involves
Urszula Fałkowska +7 more
wiley +1 more source
Addressing Unmet Needs in Prurigo Nodularis: Expert Canadian Dermatology Perspectives
Prurigo nodularis (PN) is a distinct chronic, inflammatory, neuroimmune‐mediated skin condition characterized by pruritic, often symmetrically distributed nodules, papules, and/or plaques. Recognition of PN as a distinct entity is complicated by the absence of a precise disease definition, uncertain epidemiologic estimates, and limited assessments of ...
Vimal H. Prajapati +4 more
wiley +1 more source

