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Disseminated Cutaneous Mucormycosis Developing in Peristomal Pyoderma Gangrenosum
David A Prentice1,2, Erasmia Christou3,4, Wendy A Pearson5,6
1Neurosciences, Perron Institute for Neurological and Translational Science, Perth, AUS.
Cureus
|June 26, 2024
Summary
Long-term glucocorticoid therapy for peristomal pyoderma gangrenosum (PPG) can lead to invasive mucormycosis (MM). Early skin biopsy and clinical evaluation are crucial for diagnosing and managing resistant PPG cases.
Area of Science:
- Dermatology
- Mycology
- Infectious Diseases
Background:
- Peristomal pyoderma gangrenosum (PPG) is a chronic inflammatory skin condition often managed with immunosuppressants.
- Long-term glucocorticoid therapy is a common treatment for PPG, but carries risks of opportunistic infections.
- Invasive fungal infections, such as mucormycosis (MM), are rare but serious complications associated with immunosuppression.
Observation:
- A case presentation of a patient with PPG on long-term glucocorticoid therapy who developed disseminated mucormycosis.
- The patient exhibited wound dissemination of mucormycosis, indicating a severe and invasive presentation.
- This case highlights a critical adverse event associated with the management of PPG.
Findings:
- The study emphasizes the importance of skin biopsy for diagnosing PPG, especially in cases resistant to conventional therapy or with new symptoms.
- Clinical evaluation alongside diagnostic procedures is vital for accurate and timely diagnosis.
- Long-term corticosteroid use significantly increases the risk of invasive fungal infections like mucormycosis.
Implications:
- Early detection and prompt management of mucormycosis in patients with PPG are critical for improving patient outcomes.
- Healthcare providers should be vigilant for signs of invasive fungal infections in patients on long-term glucocorticoid therapy.
- This case underscores the need for careful risk-benefit assessment when prescribing long-term immunosuppression for chronic dermatological conditions.
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