Diagnosis and Treatment of Chronic Skin Infection Caused by <em>Scedosporium apiospermum</em>

This case report presents a 77-year-old male with purplish-red, blister-like lesions on the right forearm. A background of long-term corticosteroid therapy for pemphigus led to significant immunosuppression. Initial laboratory investigations, including bacterial and fungal cultures as well as histopathological analysis, yielded inconclusive results. To identify the causative pathogen, next-generation sequencing (NGS) was performed on tissue samples, which confirmed the presence of Scedosporium apiospermum, a rare opportunistic fungus. Based on this result, a targeted treatment strategy was implemented, involving multiple surgical debridements and systemic antifungal therapy with voriconazole. The therapeutic response was favorable, with complete resolution of the infection and no signs of recurrence during an 8-month follow-up period. This case highlights the clinical value of NGS in diagnosing rare and atypical infections, particularly in immunocompromised settings where conventional methods may fail. It also underscores the importance of a multidisciplinary treatment approach that integrates timely surgical intervention with appropriate antifungal therapy to achieve optimal patient outcomes.

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Publication Details

Journal
Journal of Visualized Experiments
Published
2025-11-11
DOI
https://doi.org/10.3791/68901
Primary Topic
Autoimmune Bullous Skin Diseases
Type
article
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article

Diagnosis and Treatment of Chronic Skin Infection Caused by Scedosporium apiospermum

Ahmad Alhaskawi, Haiying Zhou, Yanzhao Dong, Qingqing Zhang et al.
Journal of Visualized Experiments
Autoimmune Bullous Skin Diseases
article

Diagnosis and Treatment of Chronic Skin Infection Caused by Scedosporium apiospermum

Ahmad Alhaskawi, Haiying Zhou, Yanzhao Dong, Qingqing Zhang, Hui Juan Lu, Weijie Zhou, Xiaodi Zou
article en

Abstract

This case report presents a 77-year-old male with purplish-red, blister-like lesions on the right forearm. A background of long-term corticosteroid therapy for pemphigus led to significant immunosuppression. Initial laboratory investigations, including bacterial and fungal cultures as well as histopathological analysis, yielded inconclusive results. To identify the causative pathogen, next-generation sequencing (NGS) was performed on tissue samples, which confirmed the presence of Scedosporium apiospermum, a rare opportunistic fungus. Based on this result, a targeted treatment strategy was implemented, involving multiple surgical debridements and systemic antifungal therapy with voriconazole. The therapeutic response was favorable, with complete resolution of the infection and no signs of recurrence during an 8-month follow-up period. This case highlights the clinical value of NGS in diagnosing rare and atypical infections, particularly in immunocompromised settings where conventional methods may fail. It also underscores the importance of a multidisciplinary treatment approach that integrates timely surgical intervention with appropriate antifungal therapy to achieve optimal patient outcomes.

Journal of Visualized Experiments(225)
People's Liberation Army 401 Hospital (CN), First Affiliated Hospital Zhejiang University (CN)
Openalex Percentile: Top 53%
Autoimmune Bullous Skin Diseases
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Diagnosis and Treatment of Chronic Skin Infection Caused by <em>Scedosporium apiospermum</em> — Ahmad Alhaskawi, Haiying Zhou, et al. · Journal of Visualized Experiments (2025) | TGRS Research Map | TGRS