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一名免疫抑制患者发生由尖端赛多孢菌引起的皮肤感染。

Cutaneous infection due to Scedosporium apiospermum in an immunosuppressed patient.

作者信息

Chaveiro M A, Vieira R, Cardoso J, Afonso A

机构信息

Department of Dermatology, Curry Cabral Hospital, Rua da Beneficiencia, no 8, 1069-166 Lisbon, Portugal.

出版信息

J Eur Acad Dermatol Venereol. 2003 Jan;17(1):47-9. doi: 10.1046/j.1468-3083.2003.00640.x.

Abstract

Scedosporium apiospermum, the anamorphic form of Pseudallescheria boydii, is a filamentous fungus with low inherent virulence. Increasing numbers of cases of this infection have been reported probably related to the rising number of immunosuppressed persons. Apart from mycetoma, cutaneous and subcutaneous infection is rarely encountered in clinical practice. We describe a case of cutaneous infection caused by Scedosporium apiospermum in a subject with rheumatoid arthritis and diabetes mellitus who was submitted to long-term therapy with cyclosporin and corticosteroids. Histopathologic examination of a skin biopsy showed a granulomatous infiltrate with hyaline septate hyphae. Culture of two skin biopsies taken at two different observations of the woman, 3 weeks apart, allowed isolation of Scedosporium apiospermum. Therapy with itraconazole, 400 mg/day, for 3 months was effective in curing the infection.

摘要

阿皮尤斯德氏霉是博伊德假阿利什霉的无性型,是一种固有毒力较低的丝状真菌。据报道,这种感染的病例数量不断增加,这可能与免疫抑制人群数量的上升有关。除了足菌肿外,皮肤和皮下感染在临床实践中很少见。我们描述了一例由阿皮尤斯德氏霉引起的皮肤感染病例,患者为类风湿性关节炎和糖尿病患者,长期接受环孢素和皮质类固醇治疗。皮肤活检的组织病理学检查显示有肉芽肿浸润及透明有隔菌丝。在该女性患者相隔3周的两次不同检查时采集的两份皮肤活检组织进行培养,均分离出了阿皮尤斯德氏霉。采用伊曲康唑400毫克/天治疗3个月,有效治愈了感染。

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