Bullous systemic lupus mimicking a Stevens-Johnson syndrome

Abstract

Autoimmune bullous diseases represent a diagnostic challenge due to the wide spectrum of pathologies that share similar clinical features. This paper reports the case of a woman admitted with a supposed diagnosis of a Stevens-Johnson syndrome, in which the history, the profile of autoimmunity and interdisciplinary approach were of vital importance to clarify the clinical picture.

Keywords

• lupus eritematoso sistémico
• vesículas
• reacción medicamentosa severa
• autoinmunidad