Results 101 to 110 of about 23,997 (201)
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
, 2002 We report a 51-year-old man with a 20-year history of chronic plaque psoriasis who developed an autoimmune subepidermal blistering eruption that had clinical features of bullous pemphigoid, erythema multiforme and epidermolysis bullosa acquisita ...
Gratian, M J +9 more
core +1 more source
Skin Research and Technology, Volume 32, Issue 1, January 2026.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
The Syk Tyrosine Kinase Is Required for Skin Inflammation in an In Vivo Mouse Model of Epidermolysis Bullosa Acquisita. [PDF]
J Invest Dermatol, 2017 The inflammatory form of epidermolysis bullosa acquisita is caused by autoantibodies against type VII collagen (C7), a component of the dermal-epidermal junction.
Németh T +3 more
europepmc +2 more sources
Skin Fragility and Hyperpigmentation in a Patient With HIV
JEADV Clinical Practice, Volume 5, Issue 2, Page 716-718, June 2026.
Catalina Retamal +2 more
wiley +1 more source
Bullous Systemic Lupus Erythematosus: Clinical Presentation in Two Asian Cases
Case 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
Mucosal Morbidity in Patients With Epidermolysis Bullosa Acquisita
, 1999 BACKGROUND Epidermolysis bullosa acquisita is an acquired inflammatory and/or dermolytic subepidermal blistering disease characterized by IgG autoantibodies to type VII collagen.
Summers, Ronald M +7 more
core +1 more source
Secondary Syphilis With Concomitant Bullous Pemphigoid: A Case Report
Case Reports in Dermatological Medicine, Volume 2026, Issue 1, 2026.A 52‐year‐old woman presented with a three‐month history of pruritic scaly palmoplantar eruptions that progressed to tense bullae over trunk and extremities along with genital mucosal involvement. Serology confirmed syphilis (VDRL reactive at 1:16 and TPHA positive), and biopsy with direct immunofluorescence (DIF) established bullous pemphigoid (BP ...
Subi Rijal +11 more
wiley +1 more source
Pyoderma Gangrenosum as the First Manifestation of Inflammatory Bowel Disease: A Case Report
Case Reports in Gastrointestinal Medicine, Volume 2026, Issue 1, 2026.Approximately 50% of patients with inflammatory bowel disease (IBD) exhibit extraintestinal manifestations, among which skin and mucosal lesions are common. However, pyoderma gangrenosum occurs in only 1%‐2% of IBD patients. We report the case of a 23‐year‐old male patient who was admitted to the hospital with pyoderma gangrenosum that was unresponsive
Nam Hoai Nguyen +7 more
wiley +1 more source
, 2018 Reduced Skin Blistering in Experimental Epidermolysis Bullosa Acquisita After Anti-TNF ...
Franziska Schulze (5816831) +13 more
core +1 more source