Pemphigus vulgaris (PV) is an autoimmune mucocutaneous blistering disorder for which early recognition and treatment are necessary to achieve a favourable prognosis. A multidisciplinary, patient-centred approach is required to optimize therapeutic outcomes. Systemic corticosteroids remain first-line treatment for PV patients, yet their optimal dosing regimen remains unknown. Further, various steroid-sparing adjuvants play an important role in the treatment of PV. As clinical trials in the field are limited by small sample sizes and a lack of standardized outcome measures, a therapeutic algorithm is presented to guide the management of PV patients.
CITATION STYLE
Shoimer, I., Wong, R. X., & Mydlarski, P. R. (2016). Pemphigus vulgaris. In Autoimmune Bullous Diseases: Approach and Management (pp. 1–18). Springer International Publishing. https://doi.org/10.1007/978-3-319-26728-9_1
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