ArticleClinical case reports2026
Bilateral Idiopathic Pyoderma Gangrenosum: A Case Report of an Atypical Presentation.
Article in Clinical case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Bilateral Idiopathic Pyoderma Gangrenosum: A Case Report of an Atypical Presentation.Clinical case reports · 2026Article
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Pyoderma gangrenosum (PG) is a rare non-infectious neutrophilic dermatosis which is characterized by a rapidly progressive, painful ulcer. Bilateral manifestation of PG is exceptionally rare and can easily be misdiagnosed as infection or vascular ulceration, delaying proper treatment. A 76-year-old woman presented with painful, crusted ulcers on her bilateral lower legs that developed over 2 weeks. Initially, the lesions erupted as erythematous papules that enlarged rapidly and ulcerated. There was no history of trauma, systemic illness, or prior ulceration. Laboratory tests revealed mild anemia and an elevated C-reactive protein level. Swab culture from the wound site showed growth of
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