A 7-year-old boy with T cell acute lymphoblastic leukemia developed di
sseminated hyalohyphomycosis due to Fusarium solani. The clinical feat
ures included fever, severe myalgia, documented fungemia with F. solan
i, an ecthyma gangrenosum-like lesion next to a peripheral venous cath
eter, and disseminated pustules. Severe neutropenia due to chemotherap
y was the most revelant risk factor. Histopathologic study of the ecth
yma gangrenosum-like lesion, as well as pustular lesions, revealed epi
dermal necrosis and an inflammatory infiltrate in the upper dermis, wi
th numerous septate hyphae demonstrated by periodic acid-Schiff stain.
Clinical resolution was achieved with granulocyte colony-stimulating
factor and amphotericin a administration. Our case suggests that the p
eripheral venous access was probably the portal of entry of the fungus
.