| Literature DB >> 33864685 |
V E Orfaly1, I Kovalenko2, S N Tolkachjov3, A G Ortega-Loayza1, R Nunley4.
Abstract
Pyoderma gangrenosum (PG) is a rare debilitating inflammatory skin disease associated with a variety of systemic diseases. Because of its rarity, PG is treated with miscellaneous immunosuppressive agents under no FDA-approved standardized treatment approach. We present four patients with PG treated with tofacitinib in the context of the six existing cases in the literature. Tofacitinib appeared to be beneficial in the small sample of patients (n=10) who failed on average 5 other systemic therapies. The majority of patients had classic PG located on lower extremities (80%, 8/10), and 20% (2/10) were peristomal. The most common comorbidity was inflammatory bowel disease (78%, 7/9). There were no negative treatment results, and 40% (4/10) had complete healing of their ulcers, while 60% (6/10) had marked clinical improvement. From our observation, tofacitinib appears to be a promising steroid-sparing adjuvant treatment in patients with refractory PG who failed other systemic therapies. This article is protected by copyright. All rights reserved.Entities:
Year: 2021 PMID: 33864685 DOI: 10.1111/ced.14683
Source DB: PubMed Journal: Clin Exp Dermatol ISSN: 0307-6938 Impact factor: 3.470