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1.
Rev Inst Med Trop Sao Paulo ; 43(3): 163-6, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-11452326

RESUMO

We report a case of cutaneous infection caused by Phialemonium curvatum GAMS et COOKE, 1983, after bone marrow transplantation. The genus Phialemonium was created by GAMS & MCGINNIS in 1983 including three new species: Ph. obovatum, Ph. curvatum and Ph. dimorphosporum, and represents an intermediate genus between Acremonium and Phialophora. Nowadays, the genus Phialemonium is considered to be a pheoid fungus which may cause the eventual lesions observed in pheo- and hyalohyphomycosis. Species of this genus have been described as opportunistic agents in humans and animals, mainly as a result of immunosuppression. In the present case, the patient had multiple myeloma and received an allogenic bone marrow transplant from his HLA-compatible brother. Two months after transplantation, he developed purplish and painful nodular lesions on the right ankle. Some of these lesions drained spontaneously and apparently hyaline mycelial filaments were observed, whose culture was initially identified as Acremonium sp. Subsequent studies showed that the fungus was Phialemonium curvatum. The infection was treated with amphotericin B, followed by ketoconazole. The patient was submitted to surgical debridement followed by two skin grafts to repair the bloody area. The duration of the treatment was 4 months and secondary prophylaxis with ketoconazole alone was maintained for one additional month. No recurrence was observed after discontinuation of treatment. The authors comment on the pathogenicity of the genus Phialemonium.


Assuntos
Transplante de Medula Óssea/efeitos adversos , Dermatomicoses/microbiologia , Fungos Mitospóricos/isolamento & purificação , Infecções Oportunistas/complicações , Adulto , Dermatomicoses/tratamento farmacológico , Humanos , Hospedeiro Imunocomprometido , Masculino
2.
J Clin Microbiol ; 39(6): 2321-4, 2001 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-11376082

RESUMO

A case of phaeohyphomycosis is reported in a male renal transplant recipient with a nodular lesion in the right leg who was treated with immunosuppressing drugs. The lesion consisted of a purulent cyst with thick walls. The cyst was excised surgically, and the patient did not receive any antifungal therapy. One year later he remains well. Histological study of the lesion showed a granulomatous reaction of epithelioid and multinucleate giant cells, with a central area of necrosis and pus. Fontana-Masson staining demonstrated the presence of pigmented hyphal elements. The fungus Colletotrichum crassipes was grown in different cultures from the cyst. The in vitro inhibitory activities of eight antifungal drugs against the isolate were tested. Clotrimazole and UR-9825 were the most active drugs. This case represents the first known reported infection caused by this rare species.


Assuntos
Colletotrichum/isolamento & purificação , Cistos/diagnóstico , Dermatomicoses/diagnóstico , Adulto , Colletotrichum/classificação , Colletotrichum/crescimento & desenvolvimento , Meios de Cultura , Cistos/microbiologia , Cistos/cirurgia , Dermatomicoses/microbiologia , Dermatomicoses/cirurgia , Humanos , Transplante de Rim , Masculino
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