Sirithanaphol Wichien, Sangkhamanon Sakkarn, Netwijitpan Sittichai, Foocharoen Chingching
Division of Urology, Department of Surgery, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
Pathology Department, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.
J Endourol Case Rep. 2018 Jun 1;4(1):91-93. doi: 10.1089/cren.2018.0038. eCollection 2018.
Malakoplakia, an anecdotal reactive granulomatous lesion, is a rare pathologic entity but relatively more common in genitourinary tracts. Here we report a case of malakoplakia in the urinary bladder in systemic sclerosis. The patient was a 66-year-old female treated with long-term corticosteroid and cyclophosphamide. She presented with gross hematuria, and cystoscopy and biopsy revealed malakoplakia. There was no tumor and the stains for infectious organism were all negative. To the best of our knowledge, this is the first case report of malakoplakia in a systemic sclerosis patient.
软斑病是一种罕见的病理实体，是一种偶见的反应性肉芽肿性病变，但在泌尿生殖道相对更为常见。在此，我们报告一例系统性硬化症患者膀胱软斑病的病例。该患者为66岁女性，长期接受皮质类固醇和环磷酰胺治疗。她出现肉眼血尿，膀胱镜检查和活检显示为软斑病。未发现肿瘤，感染性生物体染色均为阴性。据我们所知，这是系统性硬化症患者软斑病的首例病例报告。
