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Description
A 60-year-old woman presented with a large painful haemorrhagic ulcer of her left lower abdomen. Her medical history included ulcerative colitis, breast cancer, stroke and atrial fibrillation for which she was on warfarin. On examination she had a 15×6 cm large necrotic haemorrhagic ulcer of the left lower abdomen (figure 1). The border appeared violatious and undermined and the ulcer was malodorous. There was a history of trauma at the site of ulcer 2 months previously and the ulcer had since progressed. The differential diagnosis included warfarin necrosis and pyoderma gangrenosum. Biopsy specimen (figure 2) of the ulcer revealed ulceration and florid active chronic inflammation extending throughout the dermis and into subcutaneous fatty tissue confirming the clinical impression of pyoderma gangrenosum. She was started on oral prednisolone 30 mg and dapsone 50 mg daily along with regular dressings. The area of pyoderma gangrenosum showed good evidence of healing with borders appearing much flatter with evidence of shrinkage. Pyoderma gangrenosum of abdominal wall is rare and needs careful clinical and histopathological evaluation.
Learning points
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Pyoderma gangrenosum falls in the spectrum of neutrophilic dermatoses, inflammatory disorders that have in common a tendency for pathergy, as demonstrated in this case.
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Although rare, pyoderma gangrenosum can involve the abdominal wall and the early involvement of a dermatologist is extremely useful for proper diagnosis and management.
Footnotes
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Contributors GPM created the manuscript and was involved with patient care. SH was involved in making the diagnosis and JH with analysis of the pathological specimen. All authors have reviewed and had input into the manuscript.
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Competing interests None.
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Patient consent Obtained.
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Provenance and peer review Not commissioned; externally peer reviewed.