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Infliximab-induced Remission of Postoperative Pyoderma Gangrenosum: A Case Report and Literature Review
Panapipat Pratanrit1, Nathathai Pratumchart1, Kumutnart Chanprapaph1
1From the Division of Dermatology, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Plastic and Reconstructive Surgery. Global Open
|August 6, 2026
Summary
Postoperative pyoderma gangrenosum (PPG) can be challenging to diagnose and treat. Infliximab, a TNF-α inhibitor, demonstrated efficacy in healing refractory PPG, offering a steroid-sparing option.
Area of Science:
- Dermatology
- Immunology
Background:
- Pyoderma gangrenosum (PG) is a rare neutrophilic dermatosis causing painful ulcers.
- Postoperative PG (PPG) arises at surgical sites due to pathergy, often misdiagnosed.
- Delayed diagnosis of PPG can lead to ineffective treatments and surgical interventions.
Purpose of the Study:
- To report a case of refractory postoperative pyoderma gangrenosum.
- To evaluate the efficacy of infliximab in treating severe PPG.
- To review literature on TNF-α inhibitors for PPG management.
Main Methods:
- A 69-year-old male patient presented with extensive ulcerative lesions post-surgery for chronic venous insufficiency.
- Initial treatments included surgical debridements and antibiotics without improvement.
- Diagnosis of PPG was confirmed, and treatment with corticosteroids was initiated, followed by infliximab.
Main Results:
- Systemic corticosteroids provided partial improvement for the patient's PPG.
- Infliximab treatment led to complete healing of the ulcerative lesions.
- The patient achieved remission with infliximab and discontinuation of immunosuppressants.
Conclusions:
- This case underscores the importance of recognizing PPG in non-healing surgical ulcers.
- Infliximab proved effective as a steroid-sparing therapy for severe PPG.
- TNF-α inhibitors represent a viable treatment for refractory PPG.
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