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Diagnosis and Treatment Difficulty in Early-Onset Peristomal Pyoderma Gangrenosum Associated With Ulcerative Colitis:
Ken Imaizumi1, Hiroyuki Kasajima2, Kazutoshi Terashima3
1Gastrointestinal Surgery, Hakodate Municipal Hospital, Hakodate, JPN.
Insights
Peristomal pyoderma gangrenosum (PPG) is a rare condition that can complicate gastrointestinal surgery. Early suspicion and multidisciplinary management are key for treating this ulcerative skin lesion around stomas.
Area of Science:
- Dermatology
- Gastroenterology
- Surgical Wound Management
Background:
- Peristomal pyoderma gangrenosum (PPG) is a rare, challenging complication following ostomy surgery, often mistaken for infection.
- Prompt diagnosis and management are crucial for patient outcomes, yet often delayed due to low clinical suspicion.
Observation:
- An 18-year-old female developed a dehisced trocar wound post-proctocolectomy for ulcerative colitis, initially treated as infection.
- The wound progressed, leading to a diagnosis of PPG on postoperative day 37.
- Management involved topical steroids, systemic infliximab (discontinued due to allergy), and specialized wound care with hydrofiber dressings and stoma paste.
Findings:
- Successful remission of PPG was achieved with oral prednisone (30 mg/day) initiated on postoperative day 82.
- Specialized wound care, including sealing therapy and proper stoma management, was vital for exudate control and wound protection.
- The patient underwent successful stoma closure 12 months post-surgery with no recurrence of PPG.
Implications:
- This case highlights the importance of suspecting PPG in ulcerative lesions around stomas, even early postoperatively.
- A multidisciplinary approach involving dermatology, gastroenterology, and surgical teams is essential for accurate diagnosis and effective management of PPG.
- Optimized stoma care and wound sealing techniques can significantly improve outcomes for patients with PPG.
Abstract:
Peristomal pyoderma gangrenosum (PPG) is a rare dermatological condition associated with gastroenterological disease. Most gastrointestinal surgeons find it difficult to suspect and treat PPG, especially at early onset. The patient was an 18-year-old female. The patient underwent three-stage restorative proctocolectomy for refractory ulcerative colitis. On postoperative day (POD) 9, the trocar wound near the ileostomy site dehisced. Because the wound culture was positive, the wound was treated with an antibacterial agent as an infection. However, the wound worsened. The patient was referred to a dermatologist for diagnosis. PPG was diagnosed on POD 37. Wound management was initiated using topical steroids. The wound caused difficulties in pain and dressing management. Although infliximab was administered as a systemic therapy, it was discontinued because of allergic symptoms. Sealing therapy with hydrofiber dressing and adequate stoma pouching with stoma paste provided good exudate absorption and a clean environment by protecting the wound from stoma excretion. Oral prednisone was initiated on POD 82. Improvement in the wound condition was observed with a prednisone dose of 30 mg/day. Complete remission was achieved seven months after onset. Twelve months after the surgery, stoma closure was performed. The local cutaneous condition remained in remission without exacerbation. Suspicion of PPG can be difficult when it develops early after stoma creation. We never forget that PPG should be suspected when a progressive ulcerative lesion is found around the stoma, even early after operation. If PPG is suspected, a multidisciplinary team plays an essential role in its diagnosis and management.
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