Pyoderma gangrenosum in ulcerative colitis
Images in Clinical Medicine

Pyoderma gangrenosum in ulcerative colitis

Meng-You Zeng1,2, Wei Liu1,2

1Institute of Digestive Disease, China Three Gorges University, Yichang 443000, China; 2Department of Gastroenterology of Yichang Central People’s Hospital, Yichang 443000, China

Correspondence to: Wei Liu, PhD. Institute of Digestive Disease, China Three Gorges University, 8 Daxue Road, Yichang 443000, China. Email: liuwei@ctgu.edu.cn.

Received: 16 February 2020; Accepted: 10 March 2020; Published: 25 September 2021.

doi: 10.21037/amj-20-23


A 21-year-old man presented to an outpatient clinic with an 8-month history of hematochezia, abdominal pain, tiredness, and weight loss. His abdomen was soft, with mild left lower quadrant abdominal tenderness and active bowel sounds. Laboratory evaluation revealed a hemoglobin level of 10.4 g per deciliter (normal range, 13.5 to 17.5). Computed tomography of the abdomen revealed thickened wall of colon sigmoideum and rectum (Figure 1A). The colonoscopy showed congestion, edema and ulcer in the same location (Figure 1B), and mucosal biopsy by colonoscopy suggested that submucosal abscess was formed and presented as fissuring ulcers. T-SPOT.TB assay was negative. Two weeks later, the painful and rapidly progressive ulcerative lesions involving the left ankle joint was shown sequentially accompanied by red swollen (the 1st day; Figure 1C), deep ulcers (the 3rd day; Figure 1D), and necrosis (the 5th day; Figure 1E). The physical examination showed skin ulcerations with both an irregular purple and a purulent base edge. The histopathological detection of an incisional biopsy sample separated from the ankle lesion revealed both superficial dermal and epidermal necrosis with leukocytoclastic vasculitis, an underlying mixed inflammatory-cell infiltrate and abscess formation. Direct microbiologic detection and cultures were negative for bacterial and fungal pathogens. A diagnosis of pyoderma gangrenosum (PG) in ulcerative colitis was made. PG is an inflammatory skin disease with characteristics of rarity, chronicity and destructiveness, in which a painful nodule or pustule breaks down to generate a progressive and expansive ulcer with a undermined, tender and raised border (1-3). PG is usually related to systemic proinflammatory states, most particularly inflammatory bowel disease (4,5). Treatment can be extremely challenging, usually involving different kinds of immunosuppressive therapies (6,7). In this patient, the debridement was given. Treatment with sulfasalazine was initiated, and 2 weeks later, methylprednisolone therapy was started. Four weeks later, dermatoplasty was performed. The cutaneous ulcers had diminished substantially, with residual superficial atrophic scars on the 7th day after the operation (Figure 1F). He was discharged home with synchronous resolution of hematochezia and abdominal pain symptoms, as well as with outpatient follow-up.

Figure 1 Pyoderma gangrenosum in ulcerative colitis.

Acknowledgments

Funding: This work was supported by National Natural Science Foundation of China (31600134)


Footnote

Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/amj-20-23). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

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doi: 10.21037/amj-20-23
Cite this article as: Zeng MY, Liu W. Pyoderma gangrenosum in ulcerative colitis. AME Med J 2021;6:32.