A case of cutaneous malakoplakia in an 81-year-old woman in reported. A reddish slowly growing plaque had appeared on her forehead 13 years previously. Histopathology revealed a dense dermal granulomatous infiltrate consisting of lymphocytes and numerous histiocytes containing Michaelis-Gutmann bodies. Ciprofloxacin treatment resulted in partial involution of the lesion.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1159/000246136 | DOI Listing |
J Dermatol
January 2025
Department of Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan.
JAAD Case Rep
August 2024
SkinPath Solutions, Smyrna, Georgia.
Head Neck Pathol
June 2024
Division of Dental and Oral Medicine, New York-Presbyterian/Queens, Flushing, New York, USA.
BMJ Case Rep
June 2024
Obstetrics and Gynaecology, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
BMC Nephrol
June 2024
Department of Medicine, Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Malakoplakia is a rare inflammatory disorder believed to result from a defect in macrophage phagocytic function triggering a granulomatous reaction. It can present with genitourinary, gastrointestinal, or cutaneous manifestations in immunocompromised or, less commonly, immunocompetent hosts. We describe a case of renal malakoplakia in a young, otherwise healthy patient presenting with nephromegaly and sepsis following an E.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!