3.8 Article

Understanding an unusual urothelial disorder: cystitis cystica et glandularis

Journal

JOURNAL OF CLINICAL UROLOGY
Volume 16, Issue 5, Pages 526-532

Publisher

SAGE PUBLICATIONS LTD
DOI: 10.1177/20514158211032819

Keywords

Cystitis cystica; cystitis glandularis; bladder tumour; intestinal metaplasia; lower urinary tract symptoms

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Cystitis cystica et glandularis is a rare clinic pathological entity that often mimics bladder tumors. It is more common in men and presents with lower urinary tract symptoms. Transurethral resection is the main treatment method, but it is often associated with upper tract hydronephrosis. Close surveillance is necessary due to its controversial premalignant nature, recurrence, and risk of upper tract deterioration.
Objectives: To study the presentation and natural course of cystitis cystica et glandularis. Methods: A retrospective analysis of patients with histopathologically confirmed cystitis cystica et glandularis from March 2016 to March 2018 who at least completed their 2 years' follow-up was performed. Perioperative details along with the last available follow-up were included in the analysis. Results: A total of 10 patients were included. The mean age (+/- standard deviation) was 33.4 (+/- 14.0) years and nine (90%) were men. The most common presentation was storage and voiding lower urinary tract symptoms (80%) along with haematuria (40%) and dysuria (20%). Four patients had the presence of hydronephrosis in preoperative imaging, of which three patients had bilateral mild hydroureteronephrosis. All the patients underwent transurethral resection the bladder tumour as all were diagnosed with urinary bladder mass on preoperative imaging. All the patients had a trigonal lesion with a bullous appearance partially obstructing the bladder neck. Six patients underwent double J stenting in the perioperative period. The mean (+/- standard deviation) follow-up duration was 32.8 (+/- 7.5) months. Patients were kept on regular surveillance with imaging and cystoscopy as indicated. Eight patients (80%) developed recurrence in the follow-up period. The mean number of recurrences was 1.5 (+/- 1.1). One of the patients had to undergo augmentation ileocystoplasty with bilateral ureteric reimplantation because of the recurrent lesion with small contracted bladder, while another patient underwent cystectomy with urinary diversion owing to recurrence and refractory lower urinary tract symptoms. Besides, there was no evidence of malignancy after this entity in any of the patients. Conclusion: Cystitis cystica et glandularis is a rare clinic pathological entity which often mimics bladder tumour. Cystitis cystica et glandularis is common in men and often presents with lower urinary tract symptoms. Transurethral resection forms the mainstay of treatment. However, it is often associated with upper tract hydronephrosis. Its controversial premalignant nature compounded with recurrence and risk of upper tract deterioration warrants close surveillance.

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