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Journal ArticleDOI

Pyoderma gangrenosum: a review of 86 patients.

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TLDR
The clinical, histologic, and immunofluorescent findings in 86 cases of pyoderma gangrenosum seen at the Mayo Clinic between 1970 and 1983 were reviewed, finding lymphocytic vasculitis was predominant in the zone of erythema peripheral to the area of ulceration, while neutrophilic infiltrate and abscess formation were more prominent centrally.
Abstract
The clinical, histologic, and immunofluorescent findings in 86 cases of pyoderma gangrenosum seen at the Mayo Clinic between 1970 and 1983 were reviewed. Males and females were affected in equal numbers. The most frequent site of lesions was the leg. Sixty-seven patients (78 per cent) had associated systemic disease, with arthritis and inflammatory bowel disease being commonest. Cutaneous histopathologic changes varied with the site of biopsy. Lymphocytic vasculitis was predominant in the zone of erythema peripheral to the area of ulceration, while neutrophilic infiltrate and abscess formation were more prominent centrally. In most cases studied, direct immunofluorescence showed immunoglobulins and complement deposited in and around superficial and deep dermal vessels.

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Infliximab for the treatment of pyoderma gangrenosum: a randomised, double blind, placebo controlled trial

TL;DR: This study has demonstrated that infliximab at a dose of 5 mg/kg is superior to placebo in the treatment of PG and infliximab treatment should be considered in patients with PG.
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Pyoderma gangrenosum: Classification and management

TL;DR: Pyoderma gangrenosum has four distinctive clinical and histologic variants and some have morphologic and Histologic overlapping features with other reactive neutrophilic skin conditions.
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Pyoderma gangrenosum: clinicopathologic correlation and proposed diagnostic criteria.

TL;DR: Diagnostic criteria and some historical perspectives on the diagnosis of pyoderma gangrenosum are suggested.
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Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder

TL;DR: In this paper, the authors identified disease-causing mutations in the CD2-binding protein 1 (CD2BP1; GenBank accession no XM 044569) gene in the two reported families with this disorder.
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Pyoderma gangrenosum. A comparison of typical and atypical forms with an emphasis on time to remission. Case review of 86 patients from 2 institutions.

TL;DR: A retrospective analysis of the medical records of 86 patients with pyoderma gangrenosum who were evaluated and treated over 12 years at 2 university-based dermatology departments found that inflammatory bowel disease was the most common association in patients with PG, whereas hematologic disease or malignancy was most common in those with APG.
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