Results 11 to 20 of about 12,623 (164)

Esophageal Cicatricial Pemphigoid as an Isolated Involvement Treated with Mycophenolate Mofetil [PDF]

open access: yesCase Reports in Gastrointestinal Medicine, 2015
Cicatricial pemphigoid (CP) is a rare blistering autoimmune disease. Esophageal involvement occurs in widespread disease and rarely appears as the only affected organ.
Sandra Sánchez Prudencio   +8 more
doaj   +2 more sources

Dupilumab enables glucocorticoid withdrawal in refractory multisite mucous membrane pemphigoid: a case report [PDF]

open access: yesFrontiers in Medicine
BackgroundMucous membrane pemphigoid (MMP) is a mucosal-predominant, potentially scarring autoimmune subepithelial blistering disease. Although dupilumab is approved for adult bullous pemphigoid, its use in MMP remains off-label and published experience ...
Yuan Hu   +4 more
doaj   +2 more sources

Ocular cicatricial pemphigoid treated with intramuscular corticotropin injections [PDF]

open access: yesJAAD Case Reports, 2020
Edward Chen, MD   +2 more
doaj   +2 more sources

A case series of ocular involvement in bullous pemphigoid: clinical features, management, and outcomes [version 1; peer review: 2 approved]

open access: yesF1000Research, 2021
Ocular involvement in cases of bullous pemphigoid is rare and when present, the signs are usually subtle and in the form of fine tarsal scarring and dry eye disease.
Anahita Kate   +3 more
doaj   +1 more source

A case series of ocular involvement in bullous pemphigoid: clinical features, management, and outcomes [version 2; peer review: 2 approved]

open access: yesF1000Research, 2022
Ocular involvement in cases of bullous pemphigoid is rare and when present, the signs are usually subtle and in the form of fine tarsal scarring and dry eye disease.
Anahita Kate   +3 more
doaj   +1 more source

Differentiating antiepiligrin cicatricial pemphigoid from epidermolysis bullosa acquisita by indirect immunofluorescence of skin substrates lacking Type VII collagen or laminin 332: a case report and review of literature

open access: yesDermatologica Sinica, 2011
Antiepiligrin cicatricial pemphigoid (AECP) is a chronic autoimmune subepidermal blistering disease characterized by clinical features of cicatricial pemphigoid and circulating IgG antibasement membrane autoantibodies directed against laminin 332.
Chih-Pin Chen   +3 more
doaj   +1 more source

Consensus on the treatment of autoimmune bullous dermatoses: bullous pemphigoid, mucous membrane pemphigoid and epidermolysis bullosa acquisita - Brazilian Society of Dermatology [PDF]

open access: yesAnais Brasileiros de Dermatologia, 2019
: Bullous pemphigoid, mucous membrane pemphigoid and epidermolysis bullosa acquisita are subepidermal autoimmune blistering diseases whose antigenic target is located at the basement membrane zone.
Claudia Giuli Santi   +6 more
doaj   +1 more source

The role of intravenous immunoglobulin in treatment of mucous membrane pemphigoid: A review of literature

open access: yesJournal of Research in Medical Sciences, 2016
Background: Mucous membrane pemphigoid (MMP) is considered an autoimmune blistering disease that predominantly affects mucous membranes. Various treatments are available for controlling the diseases, but not all of them may respond. Materials and Methods:
Soheil Tavakolpour
doaj   +1 more source

Ocular Cicatricial Pemphigoid: Case Report

open access: yesDelhi Journal of Ophthalmology, 2013
Ocular Cicatricial Pemphigoid (OCP) is an autoimmune, progressive disorder that primarily affects the conjunctiva producing cicatrizing conjunctivitis and can progress to blindness.
Revathi Rajaraman   +2 more
doaj   +1 more source

A Case of Sloughing Brunsting-Perry Cicatricial Pemphigoid

open access: yesGraduate Medical Education Research Journal, 2022
Mentor: Corey Georgesen Program: Dermatology Type: Case Report Background: Brunsting-Perry Pemphigoid (BPP) is a rare dermatologic condition, presenting as blisters, erosions, crusts, or scars predominantly affecting the head and neck with no mucosal ...
Alfredo Siller   +2 more
doaj   +1 more source

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