Pemphigus vulgaris

0Citations
Citations of this article
3Readers
Mendeley users who have this article in their library.
Get full text

Abstract

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free