Pyoderma Gangrenosum Mimicking Necrotizing Fasciitis: A Case Report
Takahiro Hase, Akihiro Orita, Takuya Mizukami, Hiroyuki Nakamura

TL;DR
A case of pyoderma gangrenosum was initially misdiagnosed as necrotizing fasciitis, highlighting the importance of careful clinical evaluation to avoid unnecessary surgery.
Contribution
This case report emphasizes the diagnostic challenges of pyoderma gangrenosum mimicking necrotizing fasciitis and highlights key clinical clues for accurate diagnosis.
Findings
Pyoderma gangrenosum was diagnosed after ruling out infection through negative cultures and observing characteristic pustules.
Treatment with prednisolone and adalimumab led to rapid symptom resolution and no relapse.
Clinical assessment of skin lesions and fat necrosis can prevent unnecessary surgical interventions in atypical cases.
Abstract
Pyoderma gangrenosum (PG) is a rare neutrophilic dermatosis that can mimic other severe conditions, complicating diagnosis. We report a case of PG of the knee initially mistaken for necrotizing fasciitis (NF) in a 68-year-old woman who presented with knee swelling, erythema, papules, and pustules following a fall. Despite antibiotic therapy and surgical debridement for suspected NF, the patient’s fever persisted, and laboratory markers (elevated WBC and C-reactive protein) did not improve. Histopathology revealed a dense neutrophilic infiltrate, and negative cultures ruled out infection, leading to a PG diagnosis. Treatment with oral prednisolone (60 mg/day) rapidly resolved symptoms, followed by negative pressure wound therapy, skin grafting, and adalimumab initiation. The patient stabilized without relapse. Key diagnostic clues included abundant pustules, characteristic of pustular…
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Taxonomy
TopicsAutoimmune and Inflammatory Disorders · Hidradenitis Suppurativa and Treatments · Oral Health Pathology and Treatment
