Contents
pdf Download PDF pdf Download XML
160 Views
111 Downloads
Share this article
Research Article | Volume 18 Issue 3 (July-Sep, 2025) | Pages 15 - 19
An Unwonted Case of Cutaneous Mucormycosis in a De Novo Diabetic Patient
 ,
 ,
1
Junior resident, Department of Pathology, All India Institute of Medical Sciences, Mangalagiri, Andhra, Pradesh, India.
2
Additional Professor, Department of Pathology, All India Institute of Medical Sciences, Mangalagiri, Andhra Pradesh, India
3
Senior resident, Department of Pathology, All India Institute of Medical Sciences, Mangalagiri, Andhra Pradesh, India.
Under a Creative Commons license
Open Access
Received
July 1, 2025
Revised
July 16, 2025
Accepted
July 25, 2025
Published
Aug. 2, 2025
Abstract

Background: Cutaneous mucormycosis is a rare but aggressive fungal infection typically associated with immunocompromised states, particularly uncontrolled diabetes mellitus. The disease can rapidly progress to systemic involvement, requiring prompt diagnosis and intervention.

Case Presentation: A 33-year-old male with no prior medical history presented with right lower limb swelling, ulcerations, and blistering. He was found to have newly diagnosed diabetes mellitus. Despite fasciotomy and broad-spectrum antibiotic therapy, the condition progressed to necrotizing fasciitis requiring a guillotine amputation. Histopathology revealed broad, aseptate, right-angled branching fungal hyphae consistent with mucormycosis. Bacterial cultures grew Proteus mirabilis and Escherichia coli. The patient deteriorated due to septic shock and multi-organ dysfunction and succumbed despite intensive care.

Investigations: Elevated renal parameters and electrolyte imbalances were noted. Histopathology confirmed cutaneous mucormycosis. Culture reports showed a polymicrobial bacterial infection.

Intervention: Right above-knee guillotine amputation, supportive care, antifungal and antibiotic therapy.

Outcome: Despite surgical and medical management, the patient died due to complications of septic shock and multi-organ failure.

Conclusion: Cutaneous mucormycosis, although rare, should be considered in patients with rapidly progressive necrotizing soft tissue infections—even in the absence of classical signs such as black eschar. This case highlights the importance of early recognition, timely histopathological examination, and prompt surgical and antifungal management to improve outcomes.

Keywords
Recommended Articles
Case Report
Concurrent Lepra Reactions; Type 1 and Type 2 in a young male patient with borderline leprosy: Clinical and Histopathological correlation
...
Published: 02/09/2025
Original Article
Comparative Evaluation of Intralesional Corticosteroid Injection and Surgical Excision in Hypertrophic Scar Treatment
...
Published: 04/06/2022
Research Article
Efficacy of supra bioavailable itraconazole and conventional itraconazole at different dosing regimens in glabrous tinea infection
Published: 02/02/2024
Research Article
Multiple eruptive periungual pyogenic granulomas during anti-CD20 monoclonal antibody therapy for rheumatoid arthritis
Published: 19/12/2010
© Copyright Spejalisci Dermatolodzy