CASE REPORT


Pyoderma Gangrenosum of the Face: A Rare Presentation and a Rapid Resolution



Julia Shah*, Lorie Gottwald, Ashley Sheskey, Craig Burkhart
Department of Dermatology, University of Toledo College of Medicine, Toledo, USA


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© 2018 Shah et al.

open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: (https://creativecommons.org/licenses/by/4.0/legalcode). This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

* Address correspondence to this author at the Department of Dermatology, University of Toledo College of Medicine, Toledo, USA; Tel: 7346297458; E-mail: julia.shah@rockets.utoledo.edu


Abstract

Background:

Pyoderma Gangrenosum (PG) is a disorder of neutrophil chemotaxis that often affects the lower extremities of patients with concurrent autoimmune disorders.

Result and Discussion:

Resolution of lesions typically requires a minimum of six weeks of treatment with systemic steroids. We present a unique case of multifocal PG involving the hand and face that healed after ten days of treatment with oral prednisone.

Keywords: Pyoderma Gangrenosum, Neutrophil chemotaxis, Seronegative Arthritis, MCPJ, Prednisone theraphy, IgG.