Although the overall incidence of immunologic bullous diseases is comparati
vely low, they are nonetheless potentially lethal dermatologic disorders th
at occur most commonly in individuals age 55 and older. Thus familiarity wi
th the signs, symptoms,and treatments will be valuable to the primary care
physician. For bullous diseases in general, the challenge is to differentia
te between those arising from immunologic rather than exogenous causes, suc
h as drug-induced or drug-triggered pemphigus. Treatment goals include scre
ening for associated malignancies, managing the lesions, and minimizing the
morbidity and mortality associated with the disease. Collaboration with a
dermatologist can aid in achieving these objectives.