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Bullous Pemphigoid and Other Pemphigoid Dermatoses.

Authors :
Pratasava, Valeryia
Sahni, Vikram N.
Suresh, Aishwarya
Huang, Simo
Are, Abhirup
Hsu, Sylvia
Motaparthi, Kiran
Source :
Medicina (1010660X); Oct2021, Vol. 57 Issue 10, p1-14, 14p
Publication Year :
2021

Abstract

The pemphigoid family of dermatoses is characterized by autoimmune subepidermal blistering. The classic paradigm for pemphigoid, and the most common member, is bullous pemphigoid. Its variable clinical presentation, with or without frank bullae, is linked by significant pruritus afflicting the elderly. Mucous membrane pemphigoid is an umbrella term for a group of subepidermal blistering dermatoses that favor the mucosal membranes and can scar. Epidermolysis bullosa acquisita is a chronic blistering disorder characterized by skin fragility, sensitivity to trauma, and its treatment-refractory nature. Clinicians that encounter these pemphigoid disorders may benefit from an overview of their clinical presentation, diagnostic work-up, and therapeutic management, with an emphasis on the most frequently encountered pemphigoid disease, bullous pemphigoid. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1010660X
Volume :
57
Issue :
10
Database :
Complementary Index
Journal :
Medicina (1010660X)
Publication Type :
Academic Journal
Accession number :
153352946
Full Text :
https://doi.org/10.3390/medicina57101061