# A Case of Pyoderma Gangrenosum in a 40-Year-Old Male Patient: A Challenging Diagnosis

**Authors:** Jatin Goyal, Alexandra Goldman, Nicole Cardona

PMC · DOI: 10.7759/cureus.79051 · Cureus · 2025-02-15

## TL;DR

This paper reports a challenging case of pyoderma gangrenosum in a 40-year-old man, highlighting the importance of accurate diagnosis and timely treatment.

## Contribution

The novelty lies in presenting a rare and atypical case of PG with peripheral vascular disease, emphasizing diagnostic challenges and management.

## Key findings

- The patient's condition was initially misdiagnosed as cellulitis due to overlapping symptoms.
- Clinical diagnosis of PG was made based on history, lesion characteristics, and response to corticosteroids.
- The case underscores the need to consider PG in patients with non-healing ulcers and atypical presentations.

## Abstract

Pyoderma gangrenosum (PG) is a rare, immune-mediated neutrophilic dermatosis, presenting with painful ulcerative skin lesions. These lesions often start as pustules on an erythematous base, progressing to large ulcers with purulent edges. Diagnosing PG can be challenging, as it lacks definitive tests and requires exclusion of other conditions, including infections and vascular diseases. PG is frequently associated with systemic autoimmune diseases such as inflammatory bowel disease, rheumatoid arthritis, and monoclonal gammopathies. This report describes a case of a 40-year-old Hispanic male patient with recurrent, painful lesions on his lower extremities. Initially misdiagnosed as cellulitis, the patient had a complex history of peripheral vascular disease, which added to the diagnostic difficulty. The patient's history of recurrent ulcerations, persistent post-inflammatory hyperpigmentation, and rapid response to corticosteroids led to a clinical diagnosis of PG. This case highlights the need for careful differential diagnosis in chronic, non-healing lesions, emphasizing that PG should be considered, particularly in atypical presentations or in patients without common systemic associations. Early recognition and immunosuppressive therapy are crucial to avoid misdiagnosis and improve patient outcomes.

## Linked entities

- **Diseases:** pyoderma gangrenosum (MONDO:0018824), cellulitis (MONDO:0005230), inflammatory bowel disease (MONDO:0005265), rheumatoid arthritis (MONDO:0008383), peripheral vascular disease (MONDO:0005294)

## Full-text entities

- **Diseases:** peripheral vascular disease (MESH:D016491), rheumatoid arthritis (MESH:D001172), cellulitis (MESH:D002481), ulcerative skin lesions (MESH:D012883), painful (MESH:D010146), monoclonal gammopathies (MESH:D010265), inflammatory bowel disease (MESH:D015212), infections (MESH:D007239), ulcers (MESH:D014456), autoimmune diseases (MESH:D001327), neutrophilic dermatosis (MESH:D016463), vascular diseases (MESH:D014652), PG (MESH:D017511), hyperpigmentation (MESH:D017495)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC11913396/full.md

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Source: https://tomesphere.com/paper/PMC11913396