Case Report. Atypical cutaneous pseudallescheriosis refractory to antifungal agents

被引:21
作者
Ginter, G
Petutschnig, B
Pierer, G
Soyer, HP
Reischle, S
Kern, T
de Hoog, S
机构
[1] Graz Univ, Dermatol Klin, Dept Dermatol, A-8036 Graz, Austria
[2] Graz Univ, Dept Transplantat, Div Surg, Graz, Austria
[3] Cent Bur Schimmelcultures, NL-3740 AG Baarn, Netherlands
关键词
Pseudallescheria boydii; cutaneous infection; heart transplant; antimycotic chemotherapy; itraconazole; miconazole; surgical debridement;
D O I
10.1046/j.1439-0507.1999.00480.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
We report on a 65-year-old male heart transplant recipient who was otherwise in good condition. The patient was immunocompromised secondarily due to cyclosporin, prednisolone and azathioprine when widespread pustular skin lesions with erythematous margins subsequently developed on his left forearm. There was no history of trauma or septic temperature. Bacterial cultures were sterile and the results of native and cultural investigation studies were negative. A biopsy specimen of the lesion demonstrated hyalohyphomycosis with numerous septate hyphae within granulomas throughout the dermis. Subcutaneous tissues were not involved. Culture plates inoculated with pus and skin from the punch biopsy showed growth of a mould yielding Pseudallescheria boydii. Sensitivity testing was performed with miconazole, ketoconazole and itraconazole showing the best in vitro activity against P. boydii. In spite of treatment with itraconazole, the erythema and pustules continued to spread and therapy was changed to intravenous miconazole. Due to ongoing progression after 3 months of antifungal therapy surgical debridement was required. After 2 years of follow up, he had no recurrence.
引用
收藏
页码:507 / 511
页数:5
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