| Literature DB >> 35722167 |
Joao Bombardelli1, Janak Parikh2, Suat Morkuzu2, Aldona J Spiegel2.
Abstract
Pyoderma gangrenosum (PG) is a skin disorder characterized by painful, enlarging necrotic ulcers with bluish borders surrounded by advancing zones of erythema. The key histologic feature is neutrophilic infiltration of the superficial and deep layers of the dermis and the absence of microorganisms. Although rare and associated with autoimmune diseases such as rheumatoid arthritis, ulcerative colitis and Crohn's disease, the diagnosis is commonly missed at presentation and patients are often treated for infection with antibiotics and surgical debridement. We present a case of PG in a 51 year-old woman after a deep inferior epigastric perforator (DIEP) flap for breast reconstruction who was promptly diagnosed and treated with steroids with appropriate response. Our case highlights the importance of rapid diagnosis and treatment of this disease to avoid incorrect management including surgical debridement, which can exacerbate the disease and increase its morbidity.Entities:
Keywords: Breast reconstruction; Deep inferior epigastric perforator flap; Pyoderma gangrenosum
Year: 2022 PMID: 35722167 PMCID: PMC9204653 DOI: 10.1016/j.jpra.2022.05.009
Source DB: PubMed Journal: JPRAS Open ISSN: 2352-5878
Fig. 1Postoperative day 15. Extensive erythema and ulceration along the transverse abdominal incision with purulent base and violaceous border. There was active purulent drainage from the reconstructed umbilicus.
Fig. 2Abdominal wound on day of discharge (POD 24) with mucopurulent base, thin violaceous border and improved erythema.
Fig. 3Abdominal wound two months postoperatively. Erythematous shallow ulceration on both sides of the wound with mildly erythematous borders. Umbilicus with mildly erythematous superficial healing scar.
Fig. 4Abdominal wound completely healed 10 months after surgery. Widened scar with no ulceration or surrounding erythema.