Mh. Lowitt et al., CUTANEOUS MALACOPLAKIA - A REPORT OF 2 CASES AND REVIEW OF THE LITERATURE, Journal of the American Academy of Dermatology, 34(2), 1996, pp. 325-332
Malacoplakia, an inflammatory disease characterized by accumulations o
f phagocytic macrophages, occurs primarily in immunocompromised indivi
duals. Cutaneous involvement is rare. Two men, each with a renal allog
raft, had expanding nodules on the temple and perianal area (case 1) a
nd perianal, inguinal, and scrotal skin (case 2). Lesions resolved aft
er combined surgical and antibiotic therapy. Histopathologic examinati
on showed dense infiltration with large phagocytic macrophages contain
ing round, concentric, laminar Von Kossa stain-positive inclusion bodi
es. Histiocytes had positive results for CD 68, lysozyme, and alpha(1)
-antitrypsin. Electron microscopic examination demonstrated rare intra
cytoplasmic inclusion bodies with concentric electron-dense lamination
s of calcium (Michaelis-Gutmann bodies.) Cutaneous malacoplakia should
be considered in the differential diagnosis of nodules or draining ul
cers, particularly in immunocompromised patients. Because Michaelis-Gu
tmann bodies are difficult to identify, specimens should be evaluated
for cutaneous malacoplakia by immunohistochemical or electron microsco
pic means.