Resumen
Definición
Anamnesis y examen
Principales factores de diagnóstico
- presença de fatores de risco
- prurido
- vesículas tensas em uma pele normal ou eritematosa
Otros factores de diagnóstico
- placas eritematosas ou urticariformes
- lesões orais
Factores de riesgo
- idade entre 60 e 90 anos
- alelo de classe II do complexo principal de histocompatibilidade (CPH) (DQB1*0301)
- sexo masculino
Pruebas diagnósticas
Primeras pruebas diagnósticas para solicitar
- biópsia da pele para avaliação histopatológica com microscopia óptica
- biópsia de pele para teste de imunofluorescência direta
- teste da imunofluorescência indireta no soro
Pruebas diagnósticas que deben considerarse
- teste ensaio de imunoadsorção enzimática (ELISA)
Pruebas emergentes
- immunoblotting
- imunoprecipitação
- técnica de mapeamento de antígeno por sobreposição de fluorescência (FOAM)
Algoritmo de tratamiento
lesões localizadas em crianças ou adultos
lesões disseminadas em adultos
lesões disseminadas em crianças
Colaboradores
Autores
Vesna Petronic-Rosic, MD, MSc, MBA
Professor and Chair
Department of Dermatology
Georgetown University
MedStar Washington Hospital Center
Washington
DC
Divulgaciones
VPR declares that she has no competing interests.
Peer reviewers
Lawrence Parish, MD
Clinical Professor of Dermatology and Cutaneous Biology
Director
Jefferson Center for International Dermatology
Jefferson Medical College
Thomas Jefferson University
Philadelphia
PA
Disclosures
LP declares that he has no competing interests.
Timothy Patton, MD
Assistant Professor of Dermatology
Department of Dermatology
University of Pittsburgh
Pittsburgh
PA
Disclosures
TP declares that he has no competing interests.
References
Key articles
Cotell S, Robinson ND, Chan LS. Autoimmune blistering skin diseases. Am J Emerg Med. 2000;18:288-299. Abstract
Kirtschig G, Middleton P, Bennett C, et al. Interventions for bullous pemphigoid. Cochrane Database Syst Rev. 2010;(10):CD002292.Full text Abstract
Kirtschig G, Khumalo NP. Management of bullous pemphigoid: recommendations for immunomodulatory treatments. Am J Clin Dermatol. 2004;5:319-26. Abstract
Reference articles
A full list of sources referenced in this topic is available to users with access to all of BMJ Best Practice.
Differentials
- Pênfigo vulgar
- Epidermólise bolhosa adquirida
- Dermatose de imunoglobulina A (IgA) linear
More DifferentialsGuidelines
- Consensus on the treatment of autoimmune bullous dermatoses: bullous pemphigoid, mucous membrane pemphigoid and epidermolysis bullosa acquisita
- Japanese guidelines for the management of pemphigoid (including epidermolysis bullosa acquisita)
More GuidelinesCalculators
Escore de capacidade funcional de Karnofsky
More CalculatorsLog in or subscribe to access all of BMJ Best Practice
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