Unveiling the Uncommon: Pyoderma Gangrenosum as an Extraintestinal Complication of Ulcerative Colitis

Pyoderma gangrenosum (PG) is a rare inflammatory skin disorder characterized by neutrophil accumulation, commonly appearing as erythematous papules or pustules that can coalesce into extensive ulcers. It is the second most common dermatologic manifestation of inflammatory bowel disease, though it affects <1% of patients with inflammatory bowel disease. We present a case of a 66-year-old woman with a history of hypothyroidism and hypertension who developed nonhealing abdominal wounds following a small pustule. Despite multiple debridements and antibiotics, her condition worsened, alongside a history of bloody diarrhea for 2.5 years. Investigations led to a diagnosis of ulcerative colitis and PG. The patient was treated with high-dose steroids and infliximab. This case highlights the rarity of abdominal PG as an extraintestinal manifestation of ulcerative colitis and emphasizes the importance of early diagnosis and treatment in improving outcomes for affected patients.

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Journal
ACG Case Reports Journal
Published
2025-04-01
DOI
https://doi.org/10.14309/crj.0000000000001675
Primary Topic
Autoimmune and Inflammatory Disorders
Type
article
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article

Unveiling the Uncommon: Pyoderma Gangrenosum as an Extraintestinal Complication of Ulcerative Colitis

Eric Nguyen, Ali Rida, Akbar Fotouhi, Christopher Glover et al.
ACG Case Reports Journal
Autoimmune and Inflammatory Disorders
article

Unveiling the Uncommon: Pyoderma Gangrenosum as an Extraintestinal Complication of Ulcerative Colitis

Eric Nguyen, Ali Rida, Akbar Fotouhi, Christopher Glover, Edward Cay, Albert Ross, S Stefanko, Gisela Ocasio-Cortes
article en

Abstract

Pyoderma gangrenosum (PG) is a rare inflammatory skin disorder characterized by neutrophil accumulation, commonly appearing as erythematous papules or pustules that can coalesce into extensive ulcers. It is the second most common dermatologic manifestation of inflammatory bowel disease, though it affects <1% of patients with inflammatory bowel disease. We present a case of a 66-year-old woman with a history of hypothyroidism and hypertension who developed nonhealing abdominal wounds following a small pustule. Despite multiple debridements and antibiotics, her condition worsened, alongside a history of bloody diarrhea for 2.5 years. Investigations led to a diagnosis of ulcerative colitis and PG. The patient was treated with high-dose steroids and infliximab. This case highlights the rarity of abdominal PG as an extraintestinal manifestation of ulcerative colitis and emphasizes the importance of early diagnosis and treatment in improving outcomes for affected patients.

ACG Case Reports JournalVol. 12(4)
McLaren Greater Lansing (US), Michigan State University (US)
Good health and well-being
Openalex Percentile: Top 89%
Autoimmune and Inflammatory Disorders
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Unveiling the Uncommon: Pyoderma Gangrenosum as an Extraintestinal Complication of Ulcerative Colitis — Eric Nguyen, Ali Rida, et al. · ACG Case Reports Journal (2025) | TGRS Research Map | TGRS