Aboelkheir Abdalla, Hesham Bahaaeldeen, Subramanian Senthilkumar, Mahjoor Elham, Farouk Amgad, Hotait Hassan, Bagheri Fariborz
Department of Urology, Dubai Hospital, Dubai, ARE.
Department of Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, ARE.
Cureus. 2025 May 27;17(5):e84915. doi: 10.7759/cureus.84915. eCollection 2025 May.
Malakoplakia is a rare inflammatory disorder primarily affecting the urinary tract, characterized by granulomatous reactions and Michaelis-Gutmann bodies. It typically presents with nonspecific urinary symptoms, mimicking malignancies radiologically and histologically, thereby complicating diagnosis. This case describes an uncommon presentation in an 18-year-old male with hematuria and dysuria, initially misdiagnosed as a urothelial neoplasm. Accurate diagnosis required extensive histopathological analysis, revealing classic malakoplakia features. Management included endoscopic resection and ureteral stenting. This emphasizes the diagnostic challenges posed by malakoplakia, the importance of careful multidisciplinary evaluation, detailed histopathology for correct identification, and the need for early intervention and follow-up to avoid renal complications.
软斑病是一种罕见的炎症性疾病,主要影响泌尿系统,其特征为肉芽肿反应和米氏小体。它通常表现为非特异性泌尿系统症状,在影像学和组织学上类似恶性肿瘤,从而使诊断复杂化。本病例描述了一名18岁男性出现血尿和排尿困难的不寻常表现,最初被误诊为尿路上皮肿瘤。准确诊断需要广泛的组织病理学分析,结果显示出典型的软斑病特征。治疗包括内镜切除和输尿管支架置入。这强调了软斑病带来的诊断挑战、仔细的多学科评估的重要性、进行详细组织病理学检查以正确识别的必要性,以及早期干预和随访以避免肾脏并发症的必要性。