Introduction
Brunn’s cysts originate from Von Brunn’s nests, which are considered a normal variation of urothelium formed by the sequestering of epithelial nests from urothelial buds.1 Von Brunn’s nests are not visible endoscopically, but may be present in up to 90% of bladders and consist histologically of solid nests of benign urothelial cells found within the lamina propria or submucosa at the trigone.1 Bladder outlet obstruction caused by Brunn’s cysts is rare, with limited reported cases in the literature, all of which are described in males.2–4
Case report
A previously healthy 37-year-old male was referred with new-onset obstructive voiding symptoms. He had been complaining of weak stream, hesitancy, straining, and incomplete emptying for two months, with an International Prostate Symptom Score (IPSS) of 10 and bother score of 5. He denied gross hematuria, dysuria, nocturia, urinary incontinence, urinary tract infections, or any history of smoking or bladder irritants. Urinalysis, urine culture, and renal function studies were normal. Ultrasound of the kidneys, ureter, and bladder showed a 1.7 cm thin-walled midline cystic structure in the bladder neck, abutting the ureteric orifice (Fig. 1) without hydronephrosis. He had an elevated post-void residual (PVR) volume of 110 ml.
Fig. 1.
Bladder ultrasound depicting cystic mass at anterior bladder neck.
Cystoscopic examination demonstrated a spherical mass at the 12 o’clock position anteriorly on the bladder neck, seen best on retroflexion (Fig. 2A). The mass can be seen causing a ball-valve effect at the bladder neck (Fig. 2B). The rest of bladder was found to be unremarkable, with normal urothelium and ureteric orifices. The mass was separate from the prostate, which was small and non-obstructing (Fig. 2C). The patient was taken to the operating room for a transurethral resection of the bladder neck lesion (Fig. 2D). The mass deflated upon resection and there was no evidence of any solid components. At followup one month after surgery, the patient’s obstructive voiding symptoms had completely resolved and his PVR was 0 ml. The patient’s repeat IPSS score was 2 with a bother score of 1. Final pathology report was consistent with a Brunn’s cyst with no evidence of dysplasia or malignancy.
Fig. 2.
Cystoscopic evaluation of patient. (A) Brunn’s cyst seen on retroflexion; (B) anterior cyst seen at bladder neck; (C) verumontanum and normal prostatic urethra; and (D) retroflexion view post-transurethral resection.
The differential diagnosis of other cystic lesions near the bladder neck should always be considered. Cystitis cystica — reactive chronic inflammation secondary to bladder irritants — typically leads to small filling defects within the bladder wall, and can also manifest as a large cystic lesion.5 In these patients, inflammatory cells are commonly seen on urine cytology and the bladder mucosa has an inflammatory appearance.6 Cystitis glandularis is also associated with chronic inflammation leading to glandular metaplasia. Cystitis glandularis can also cause hematuria and has been reported to cause acute urinary retention.7 Infravesical cystic lesions in the prostate are rare, but have been reported to be associated with lower urinary tract symptoms as well.8 Most prostatic cystic lesions are found incidentally on imaging and can been classified as medial cysts, cysts of the ejaculatory duct, parenchymal cysts, infectious cysts, cystic tumors, or cysts secondary to parasitic disease.9 Ureteroceles from ectopic ureteric insertions can also appear as cystic structures near the bladder neck. However, the majority are congenital, associated with duplex collecting systems, and present in childhood.10
Conclusions
Brunn’s cyst is a rare cause of bladder outlet obstruction and can be considered in young patients with new-onset obstructive lower urinary tract symptoms. First-line treatment has been universally described as transurethral deroofing and resection, which results in durable resolution of voiding symptoms with no reported recurrences.2–4 Given the benign nature of the pathology, routine surveillance in the absence of symptoms appears to be unnecessary.
Footnotes
Competing interests: The authors report no competing personal or financial interests related to this work.
This paper has been peer-reviewed.
References
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