| Literature DB >> 25550882 |
Ye Wang1, Xiang-Chun Han2, Li-Qiang Zheng3, Wen-Long Miao4.
Abstract
Xanthogranulomatous cystitis is a rare, benign chronic inflammatory disorder with unclear etiology. Since its similar features to bladder neoplasm, it is extremely easy to be mistaken for malignant tumor. We herein reported a case of xanthogranulomatous cystitis in a 54-year-old male who presented with low abdominal pain and painless, total macrohematuria. Microscopy showed proliferation of large foam histiocytes which expressed CD68 and vimentin. Ki-67 showed a lower proliferation index (< 10%). Histopathology and immunohistochemical findings confirmed the diagnosis. This case highlighted the significance of recognizing this unusual lesion and differentiating it from its histological mimics by immunohistochemical staining.Entities:
Keywords: CD68; Ki-67; Xanthogranulomatous cystitis; neoplasm; vimentin
Mesh:
Substances:
Year: 2014 PMID: 25550882 PMCID: PMC4270612
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625