Results 71 to 80 of about 3,045,581 (181)

Bullous Pemphigoid in Children: Sustained 8‐Year Remission After Short‐Course Corticosteroid Therapy

open access: yesClinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT This article reports a case of bullous pemphigoid (BP) in a 5‐year‐old child who achieved sustained remission for up to 8 years following short‐course systemic corticosteroid therapy, aiming to provide observational evidence for the clinical management of childhood BP. The child initially presented with pruritic rashes and blisters, which were
Fengchang Wang   +3 more
wiley   +1 more source

Linear IgA bullous dermatosis in a two-year-old child: possible association with aspirin

open access: yes, 2017
A child with linear IgA bullous dermatosis, appeared after after administration of aspirin, is herein ...
Guerriero, Cristina   +6 more
core   +1 more source

Navigating the Complexities of Pemphigus Vulgaris: A Comprehensive Iranian Study

open access: yesImmunity, Inflammation and Disease, Volume 14, Issue 2, February 2026.
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

Blisters Don't Lie: Celiac Disease in the Skin

open access: yes
United European Gastroenterology Journal, Volume 14, Issue 7, September 2026.
Jonas F. Ludvigsson, Philip Curman
wiley   +1 more source

Bullous Systemic Lupus Erythematosus: Clinical Presentation in Two Asian Cases

open access: yesCase Reports in Medicine, Volume 2026, Issue 1, 2026.
Bullous systemic lupus erythematosus (BSLE) is a rare subset of systemic lupus erythematosus (SLE), characterized by the rapid onset of vesiculobullous lesions that primarily affect sun‐exposed areas of the body. These lesions typically form along the dermal–epidermal junction and are associated with the presence of autoantibodies that target the skin.
Phuong Thi Thanh Nguyen   +5 more
wiley   +1 more source

Linear IgA bullous dermatosis associated with iga nephropathy: Case report

open access: yes, 2007
Linear IgA bullous dermatosis is a rare autoimmune disease characterized by subepidermal blister formation and linear IgA deposition in the dermoepidermal junction. Linear IgA bullous dermatosis seems to be associated with several chronic diseases.
Eksioglu, Meral   +6 more
core  

Risk of persistent hypogammaglobulinaemia in children with autoimmune bullous dermatoses treated with rituximab

open access: yes
Journal of the European Academy of Dermatology and Venereology, Volume 40, Issue 7, Page e569-e574, July 2026.
S. Benkimoun   +14 more
wiley   +1 more source

Autoimmunity to Collagen XVII (BP180‐Ag2) in Pemphigoid Associated With Parkinson’s Disease

open access: yesCase Reports in Dermatological Medicine, Volume 2026, Issue 1, 2026.
The association between Parkinson’s disease and autoimmune disease is rare; in our population, there is 1 case per 10,000 inhabitants. Bullous pemphigoid has a much lower incidence, and consequently, the association of Parkinson’s disease and bullous pemphigoid is rarer.
Ricardo Cid-Puente   +6 more
wiley   +1 more source

Linear IgA bullous dermatosis: a case description

open access: yes, 2004
Linear IgA bullous dermatosis (LABD) is an immune-mediated subepidermal vesiculobullous eruption that occurs in both adults and children. It has been defined on the basis of a unique immunopathology consisting of a linear deposition of IgA along the ...
ATZORI, LAURA   +3 more
core   +1 more source

Progressive Linear Bullous Eruption in a Young Athlete: A Diagnostic Challenge

open access: yes
Journal of Paediatrics and Child Health, Volume 62, Issue 5, Page 894-896, May 2026.
Chon‐Wai Jeremy Chan   +4 more
wiley   +1 more source

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