The case of a 66-year-old woman with Gushing syndrome and a 1-year history
of papulo-nodular lesions on the right leg is reported. Biopsy revealed sep
tate hyphae and yeast-like cells in granulomatous dermo-hypodermal lesions.
Culture of biopsy fragments on Sabouraud glucose agar without cycloheximid
e produced colonies that were olive green on top and greenish black underne
ath. On the basis of microscope findings and scanning electron microscopy o
bservation of fragments of colonies, a diagnosis of cutaneous phacohyphomyc
osis due to Cladosporium oxysporum was made. The patient was initially trea
ted with itraconazole, which led to clinical improvement, but mycological r
ecovery was obtained after a course of ketoconazole, made necessary by the
presence of pituitary adenoma. To our knowledge, this is the first reported
case of subcutaneous phacohyphomycosis due to Cl. oxysporum.