Malakoplakia is a rare granulomatous infectious process that affects patients with primary or secondary immunodeficiency. 1 Abnormal macrophage bactericidal activity leads to mass-forming aggregates of histiocytes containing bacteria and pathognomonic basophilic inclusions called Michaelis-Gutmann bodies (MGB). [2][3][4][5][6] The latter are concentrically laminated, round to ovoid concretions of calcium and iron that form within phagolysosomes with bacteria. Histiocytes containing MGB are called "von Hansemann cells" in honor of the pathologist who first described them. The most common site of involvement is the genitourinary (GU) tract, but lesions have been documented in the gastrointestinal (GI) tract, lungs, skin, bone, conjunctiva, adrenal gland, and very rarely in the liver. 7 Of approximately 40 cases of cutaneous malakoplakia documented in the literature, just 4 affected pediatric patients. 1,5,[8][9][10] Only 7 cases of