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DOI 10.1016/j.ijscr.2022.107048

Медицинская библиотека · International journal of surgery case reports · 2022

A rare case of cutaneous mucormycosis in the forearm: A case report.

Shadidi-Asil Rouzbeh, Kialashaki Mehrnoosh, Fateh Armin, Ramezani Amirreza, Zamani Amir, Ebrahimian Manoochehr

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Аннотация

INTRODUCTION AND

IMPORTANCE

Cutaneous Mucormycosis (CM) is a less frequent type of fungal infection that can present with different skin lesions. Although these lesions appear to be benign and silent, CM rapidly progresses into the deeper layers. Given that no specific laboratory or imaging finding is described for the disease, the diagnosis is mainly based on history and physical examination. In addition, immediate debridement and antifungal agents must be commenced.

CASE PRESENTATION: We present a 43-year-old septic man who was hospitalized for his forefoot infection. During his admission, he developed a necrotic-like ulcer in his antecubital fossa. After initial debridement, pathology examination revealed the infection with mucormycosis. We administered intravenous liposomal Amphotericin B, and also multiple surgeries were performed. Unfortunately, the sepsis progressed to multiorgan failure, and the patient passed away.

CONCLUSION

CM requires emergent diagnosis and treatment. Early surgical interventions like extensive debridement and repetitive wound irrigation alongside systemic antifungal therapy are the key steps to preventing the progression of the disease.

Для цитирования: Shadidi-Asil Rouzbeh, Kialashaki Mehrnoosh, Fateh Armin, Ramezani Amirreza, Zamani Amir, Ebrahimian Manoochehr. A rare case of cutaneous mucormycosis in the forearm: A case report.. International journal of surgery case reports. 2022. DOI: 10.1016/j.ijscr.2022.107048.
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