Evidence map›Paper›PMID 41847105›Full record

ArticleInternational journal of surgery case reports2026

Pyoderma gangrenosum: a case report highlighting the importance of early diagnosis and treatment.

Sarah J Hayek, Robert T Brodell, Jeffrey S Doolittle, Jeremy D Jackson

Abstract readCase Reports
In one paragraph

Article in International journal of surgery case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Sarah J HayekSchool of Medicine, University of Mississippi Medical Center, Jackson, Mississippi, USA.ORCID https://orcid.org/0009-0003-8918-356X
Robert T BrodellDepartment of Dermatology, University of Mississippi Medical Center, Jackson, Mississippi, USA.
Jeffrey S DoolittleDepartment of Surgery, Delta Health System, Greenville, Mississippi, USA.
Jeremy D JacksonDepartment of Dermatology, University of Mississippi Medical Center, Jackson, Mississippi, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Pyoderma gangrenosum (PG) is a rare neutrophilic dermatosis that occurs spontaneously or after trauma, including surgery - a phenomenon known as pathergy. Postsurgical PG (PSPG) is often misdiagnosed as a pyogenic infection, leading to inappropriate interventions. Surgeons should be familiar with this complication, especially in resource-limited settings where access to specialty care is limited. Early recognition and prompt treatment significantly improve outcomes. Presentation of Case: A 65-year-old male developed erythema and edema surrounding the incision, and systemic inflammation within 48 hours of elective left inguinal hernia repair. Despite oral antibiotics, the wound rapidly deteriorated by postoperative day 6 (POD6). Repeated cultures remained negative. Markedly increased C-reactive protein (CRP) and ferritin indicated severe systemic inflammation, prompting a presumptive diagnosis of PSPG. High-dose IV corticosteroids were initiated on POD7 with rapid clinical improvement in erythema, edema, and ulceration size. He was transitioned to oral prednisone and later to oral cyclosporine, achieving complete re-epithelialization by POD32. Colchicine was initiated for maintenance therapy. Molecular testing revealed a PLCG2 mutation. One year later, a subsequent surgical procedure was performed utilizing prophylactic immunosuppression without recurrent PSPG. Discussion: This case highlights the diagnostic challenge of PSPG. Misdiagnosis may lead to surgical debridement that can worsen the condition due to pathergy. Immunosuppressive therapy, avoidance of additional trauma, and prophylactic immunosuppression prior to subsequent surgeries are mainstays of treatment. Emerging genetic associations, such as PLCG2 mutations, offer insight into the pathogenesis of PSPG. Conclusion: Early clinical recognition and prompt immunosuppression are central to management. Serial patient-acquired photographs can support monitoring and guide treatment decisions.

Indexed as

case reportinflammatory markerspathergypyoderma gangrenosumulceration

Identifiers

PMID41847105
PMCPMC12991567

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