Wang Ye, Han Xiang-Chun, Zheng Li-Qiang, Miao Wen-Long
Department of Urinary Surgery, Tangshan Gongren Hospital Tangshan, P. R. China.
Department of Pathology, The First Affiliated Hospital to Hebei North University Zhangjiakou, P. R. China.
Int J Clin Exp Pathol. 2014 Oct 15;7(11):8255-8. eCollection 2014.
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.
黄色肉芽肿性膀胱炎是一种罕见的良性慢性炎症性疾病,病因不明。由于其与膀胱肿瘤有相似特征,极易被误诊为恶性肿瘤。我们在此报告一例54岁男性黄色肉芽肿性膀胱炎病例,该患者表现为下腹部疼痛及无痛性全程肉眼血尿。显微镜检查显示大量泡沫状组织细胞增生,这些细胞表达CD68和波形蛋白。Ki-67显示增殖指数较低(<10%)。组织病理学和免疫组化结果确诊了该病。该病例强调了认识这种不寻常病变并通过免疫组化染色将其与组织学上相似的病变相鉴别的重要性。