| Literature DB >> 18062216 |
Isao Taguchi1, Tomoaki Terakawa, Hiroyuki Tsunemori, Osamu Imanishi, Nozomu Yamanaka, Takeshi Kondo, Rieko Ito.
Abstract
Malacoplakia is a relatively rare form of chronic granulomatous inflammation. Which occurs most frequently in the genito-urinary system, but renal parenchymal involvement is rare. We present a case of malacoplakia of the renal parenchyma. A 69-year-old woman with left renal mass was referred to our department. Abdominal enhanced CT scan revealed heterogeneous mass in the left kidney (50 x 45 mm). CT-guided percutaneous left renal needle biopsy confirmed the diagnosis of renal malakoplakia. We successfully treated her with oral levofloxacin. The lesion resolved after the 4-months-therapy, and there has been no recurrence for 22 months since the treatment.Entities:
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Year: 2007 PMID: 18062216 DOI: 10.5980/jpnjurol1989.98.839
Source DB: PubMed Journal: Nihon Hinyokika Gakkai Zasshi ISSN: 0021-5287