Marques, Silvio Alencar [UNESP]Camargo, R. M. P.Summerbell, R. C.De Hoog, G. S.Ishioka, P.Chambo-Cordaro, L. M.Marques, Mariângela Esther Alencar [UNESP]2014-05-202014-05-202006-11-01Medical Mycology. Abingdon: Taylor & Francis Ltd, v. 44, n. 7, p. 671-676, 2006.1369-3786http://hdl.handle.net/11449/11607A 49-year-old renally transplanted man, under a five-year course of immunosuppressive therapy with prednisone and cyclosporine A, experienced a subcutaneous phaeohyphomycosis caused by Phaeoacremonium parasiticum. The clinical presentation consisted of impressive, large, inflammatory and draining cystic tumors on the left foot that had been present for one year. A significant improvement was obtained with itraconazole plus intralesional injection with amphotericin B. Drug interaction was observed between itraconazole and cyclosporine A causing a severe hypertensive crisis and requiring a temporary sharp reduction in cyclosporine administration. Subcutaneous phaeohyphomycosis caused by P. parasiticum is uncommon among major organ transplant patients but several cases have previously been published and some patterns are emerging, e. g., limbs are generally involved but no known traumatic event has preceded lesion development. The identification of the case isolate was confirmed using a recently published online system based in part on beta-tubulin sequence comparison.671-676engsubcutaneous phaeohyphomycosisPhaeoacremonium parasiticumkidney transplantimmunosuppressive therapyArtigo10.1080/13693780600895181WOS:000242552000014Acesso restrito87894804583775527528116925519142