Bullous Pemphigoid, a clinical case

Authors

  • Filipa Moleiro Serviço de Medicina I (HEM- CHLO)
  • Nadine Monteiro Serviço de Medicina I (HEM- CHLO)
  • Rui F. Marcos Serviço de Medicina I (HEM- CHLO)
  • Graça Lérias Serviço de Medicina I (HEM- CHLO)
  • Alberto Mello e Silva Serviço de Medicina I (HEM- CHLO)

DOI:

https://doi.org/10.24950/rspmi.1009

Keywords:

Bullous pemphigoid, autoimmune subepidermal bullous dermatosis

Abstract

Bullous Pemphigoid is the most common autoimmune blistering disease,
characterized by the presence of subepidermal blisters. The authors present a case control of bullous pemphigoid (generalized bullous form) in an
80-year-old-woman with diagnosis based on a careful anamnesis and examination, treated with systemic corticoid and tetracycline as well as local treatment, having been followed up for one year. Due to its high mortality
rate it is important to recognize and treat it as early as possible. A photographic follow-up and a brief review on this matter have been made with reference to some advances.

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References

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Additional Files

Published

2014-09-30

How to Cite

1.
Moleiro F, Monteiro N, F. Marcos R, Lérias G, Mello e Silva A. Bullous Pemphigoid, a clinical case. RPMI [Internet]. 2014 Sep. 30 [cited 2024 Nov. 25];21(3):25-9. Available from: https://revista.spmi.pt/index.php/rpmi/article/view/1009

Issue

Section

Images in Medicine

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