Yoshimura Shohei, Hattori Kengo, Tsuji Emi, Tsugawa Jiro
Department of Pediatric Surgery, Takatsuki General Hospital, Takatsuki, JPN.
Department of Pediatric Surgery, Hyogo Prefectural Kobe Children's Hospital, Kobe, JPN.
Cureus. 2025 May 21;17(5):e84576. doi: 10.7759/cureus.84576. eCollection 2025 May.
A six-year-old girl was admitted to our hospital with rectal prolapse, urinary frequency, urinary stone drainage, and recurrent febrile urinary tract infections. A urinary culture identified , and an ultrasonography demonstrated mucosal calcification of the bladder wall, leading to the diagnosis of encrusted cystitis. Antibiotic administration and transurethral resection of bladder calcification were performed, and her symptoms gradually disappeared. Encrusted cystitis is extremely rare in childhood and is frequently observed in patients with post-renal transplantation, urological interventions, and immunosuppressive status. She did not have these predisposing factors; thus, bladder and bowel dysfunction may be a potential risk factor for encrusted cystitis.
一名六岁女孩因直肠脱垂、尿频、尿路结石排出及反复发热性尿路感染入院。尿液培养鉴定出……,超声检查显示膀胱壁黏膜钙化,从而诊断为结痂性膀胱炎。给予抗生素治疗并经尿道切除膀胱钙化,她的症状逐渐消失。结痂性膀胱炎在儿童期极为罕见,常见于肾移植术后、泌尿外科干预及免疫抑制状态的患者。她没有这些易感因素;因此,膀胱和肠道功能障碍可能是结痂性膀胱炎的一个潜在危险因素。