Cutaneous aspergillosis commonly occurs in immunocompromised hosts and may
also complicate burn wounds. Pseudoepitheliomatous hyperplasia (PH) is a hi
stologic reaction secondary to a wide range of stimuli, including fungal in
fection. We describe a case of an 18-year-old man, status-post burns over 7
0% of his total body surface area, with cutaneous aspergillosis of the axil
la and secondary PH. A single case of PH secondary to primary aspergillosis
has been described in the larynx but, to our knowledge, has never been des
cribed cutaneously. Histologic examination of the lesion reveals an irregul
arly acanthotic epidermis with deep invaginations within the dermis. There
is an intense inflammatory reaction within the superficial and deep dermis.
Numerous fungal forms are identified within the dermis. Special stains dem
onstrate septate hyphae with dichotomous branching, which is morphologicall
y consistent with Aspergillus. Therefore, we conclude that cutaneous asperg
illosis should be included in the differential diagnosis of causes of PH, e
specially in a patient population at risk for this infection.