Bougrine Imad, Imrani Kaoutar, Naggar Amine, Retal Hamza, Billah Nabil Moatassim, Nassar Ittimade
Radiology department, Ibn Sina University Hospital, Mohammed V University, Rabat Morocco.
Radiol Case Rep. 2024 Mar 23;19(6):2357-2361. doi: 10.1016/j.radcr.2024.02.114. eCollection 2024 Jun.
Cystitis glandularis is a rare benign condition, occurring in only 1% of the general population, and it tends to affect males more frequently. This pathology is characterized by reactive metaplasia of the bladder's urothelium, which results from chronic and recurrent irritation of the bladder wall. Symptoms are nonspecific and primarily marked by an irritative urinary syndrome accompanied by hematuria. We present a case of a young male patient with cystitis glandularis, discovered as a result of bilateral uretero-hydronephrosis detected during an ultrasound examination subsequent to an irritative urinary syndrome. The diagnosis was initially suggested by a CT scan; it was ultimately histologically confirmed following the endoscopic resection of the tumor.
腺性膀胱炎是一种罕见的良性疾病，仅在1%的普通人群中出现，且男性更易患病。这种病理状况的特征是膀胱尿路上皮的反应性化生，它是由膀胱壁的慢性和反复刺激引起的。症状不具特异性，主要表现为刺激性尿路综合征并伴有血尿。我们报告一例年轻男性腺性膀胱炎患者，该病例是在出现刺激性尿路综合征后进行超声检查时发现双侧输尿管肾积水而被诊断出来的。最初通过CT扫描提出诊断；最终在肿瘤内镜切除后经组织学确诊。
