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Pyoderma Gangrenosum Following Cesarean Section: A Case Report With Individualized Management
Zepeng Zheng1, Shilian Xu1, Xiaomiao Zeng2
1Department of Obstetrical, Shenshan Medical Central, Memorial Hospital of Sun Yat-sen University, Shanwei, China.
Case Reports in Obstetrics and Gynecology
|June 29, 2026
Summary
Severe pyoderma gangrenosum (PG) after cesarean section is rare and often misdiagnosed. Early triple immunosuppressive therapy, including corticosteroids, cyclosporine, and etanercept, effectively managed this severe case.
Area of Science:
- Dermatology
- Immunology
- Obstetrics & Gynecology
Background:
- Pyoderma gangrenosum (PG) is a rare neutrophilic dermatosis causing necrotizing skin ulcers.
- PG following cesarean section (CS) is exceptionally rare and often mistaken for surgical site infections, leading to delayed or incorrect treatment.
Purpose of the Study:
- To report a rare case of severe pyoderma gangrenosum following cesarean section.
- To highlight the diagnostic challenges and effective management strategies for post-cesarean PG.
Main Methods:
- A 24-year-old woman developed rapidly progressing ulcers post-CS, initially treated as infection.
- Diagnosis of PG was confirmed via clinical presentation, sterile cultures, and histopathology.
- Treatment involved triple immunosuppressive therapy: methylprednisolone, cyclosporine, and etanercept.
Main Results:
- The patient experienced rapid disease progression and pathergy after debridement.
- Triple immunosuppressive therapy led to rapid disease control and complete epithelialization within four months.
- No recurrence or adverse drug reactions were observed during follow-up.
Conclusions:
- Post-cesarean PG requires high clinical suspicion to differentiate from infections.
- Early and aggressive triple immunosuppressive therapy is an effective strategy for severe cases, enabling corticosteroid dose reduction.
- This approach achieved sustained remission in a severe case of post-cesarean PG.
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