Bladder stone causing vesicovaginal fistula and migration into the vagina
- Parag Sonawane ,
- Vyshnavi Sathish and
- Mehwash Nadeem
- Department of Urology, James Cook University Hospital, Middlesbrough, UK
- Correspondence to Dr Parag Sonawane; drparag.sonawane@gmail.com
Abstract
Bladder stone is a known complication in a neurogenic bladder that can very rarely cause vesicovaginal fistula (VVF). We are presenting the case of a woman in her late 70s, bed bound with progressive multiple sclerosis (MS), who was referred to urology for consideration of suprapubic catheter due to difficulty in managing her indwelling urethral catheter. The ultrasonogram (USG) identified a 4.7 cm bladder stone with right-sided hydronephrosis (HN) and left atrophic kidney. A CT scan later showed that a 5 cm bladder stone has migrated through a VVF into her vagina. She had a cystoscopy and transvaginal retrieval of the stone. Given her performance status and intraoperative finding of a small contracted bladder, it was agreed to manage her VVF conservatively.
To the best of our knowledge, this is the first case of a primary bladder stone migrating into the vagina through a VVF.
Background
Neurogenic bladder is commonly associated with urinary stasis and urinary tract infections that can lead to bladder stone formation, more so, in patients managed with indwelling urinary catheters. It can present with frequent catheter blockages and pericatheter leaks.
This case report highlights a very rare complication of bladder stone where it caused pressure necrosis of the bladder wall leading to vesicovaginal fistula (VVF) formation. The stone then migrated in the vagina and was causing rectal pain and bleeding and if left untreated could result in rectovaginal fistula, sepsis and significant risk of mortality.
This case emphasises the importance of understanding the common and serious complications associated with neurogenic bladder especially in patients with indwelling catheters. If there is a persistent problem with catheter management, further evaluation by a urologist must be considered.
Case presentation
We present a case of a woman in her late 70s with a background of progressive multiple sclerosis (MS); severely affecting her mobility (WHO performance status 4) and quality of life. Other comorbidities included insulin-dependent diabetes mellitus and Crohn’s disease.
She was managed with an indwelling urethral catheter for the past 20 years but was never under urology review. For the last 18 months, her carers were experiencing difficulty in managing her catheters, such as pericatheter leaks and blockages requiring frequent catheter change. She was referred to urology in early 2021 for consideration of a suprapubic catheter (SPC). An urgent referral for general surgery review was also made by the general practitioner (GP) at the same time, for evaluation of per rectal bleeding and a possible rectal mass on digital rectal examination.
Investigations
A ultrasonogram (USG) was done for initial evaluation that demonstrated a 4.7 cm bladder stone (figure 1). There was right-sided hydronephrosis (HN) and an almost atrophic left kidney. The blood results showed a white blood cell count (WBC) of 9.2, haemoglobin of 117 g/L and the inflammatory marker, C reactive protein was 8 mg/L. Though the renal function was stable at the time of presentation with an estimated glomerular fraction rate of 73 mL/min and serum creatinine of 69 µmol/L;, the patient was deemed to be at risk high risk of losing the function of the solitary functioning right kidney as a complication of long-standing bladder stone.
A ultrasonogram image showing bladder calculus.
In the meantime, the general surgery team requested a CT scan for evaluation of suspected rectal mass. The CT scan showed that the stone is actually in the vagina along with a few small calculi in the bladder (figure 2).
(A) CT scan sagittal image showing a large stone in the vagina, small bladder calculus and Foley bulb at the level of vesicovaginal fistula (VVF); (B) Line diagram showing the relevant pelvic anatomy (figure 2B created by authors).
Since this was her first presentation at our institute, access to previous scans was difficult but was made possible after due diligence by our team and the consultant radiologist, finally scans dating back to 2010 could be successfully retrieved and reviewed. These scans were done for non-urological indications and the patient was never referred to urology in the past.
It was then concluded that her bladder stone was seen on the scans dating from 2010 to 2014 which then migrated into the vagina where it continued to grow in size (figure 3). This could be from pressure necrosis, leading to VVF. This fairly big size stone likely obstructed both ureteric orifices leading to an atrophic left kidney and right HN (figure 4).
Previous CT scan showing bladder stone.
CT scan showing left atrophic kidney and right hydronephrosis.
The case was rediscussed in the endourology and pelvic floor multidisciplinary team meetings and the teams were in agreement that the upper tract dilation is most likely caused by the thick-walled bladder and extraluminal compression from the stone. There was no filling defect in the right ureter on delayed CT urogram images. A further discussion was held with the patient and her next of kin. Concerns surrounding the size of the vaginal stone were expressed to the family, with the acknowledgement that if left alone it could lead to a rectovaginal fistula due to ongoing pressure. Due to the fragility of the tissue, it was agreed that simultaneous VVF repair might not provide the best outcome.
Differential diagnosis
Bladder stones can cause frequent blockages and pericatheter leaks in patients with long-term catheters. Further evaluation with examination and imaging helped in reaching the diagnosis of an underlying VVF with a significant size bladder stone which was initially thought to be a rectal mass.
Treatment
On cystoscopy, the urethra was wide open due to long-term indwelling urethral catheter. VVF was found to be extending from the bladder neck up to the trigone and leading to the vagina posteriorly (figure 5). The bladder mucosa was assessed after blocking the VVF with the finger and appeared normal with no squamous metaplasia. Bladder capacity was less than 50 mL. On speculum examination, a large stone in the vagina was identified which was subsequently retrieved transvaginally with the use of cystolithotomy forceps (figure 6). The remaining small vesicle calculi were also removed. The patient was discharged home without a catheter with the advice of managing her urinary incontinence with continence pads.
Vesicovaginal fistula with a probe across.
Calculus in vagina (A) and postsurgical removal (B).
Outcome and follow-up
At 4 week follow-up, the patient was recovering well. On examination, it was noted that the fistulous communication was still present, though has become slightly smaller in size. Further discussion was conducted in the outpatient clinic regarding the long-term management of the VVF. The pros and cons of surgical repair of fistula versus conservative management were discussed in detail. It was explained to the patient and her next of kin, that due to the quality of tissue and a very small capacity bladder, the chances of success are limited. It is quite likely that her VVF is acting as a safety net for her upper renal tract and hence closing the VVF may lead to compromise of her solitary kidney. In addition to this, the patient is bed-bound so even after VVF repair will need either long term catheter (LTC) or continence pads to manage her bladder.
On a balance, it was agreed to manage her VVF conservatively. On 6 monthly follow-up, the patient is keeping well and has stable renal function. She will be on annual surveillance with USS and renal function test, given her solitary functioning right kidney.
Discussion
Bladder stones are common in patients with neurogenic lower urinary tract dysfunction.1 In one study the incidence of bladder stones in patients with spinal cord injury was 3.3%, with higher incidence, in those with suprapubic and transurethral catheter than those practicing intermittent catheterisation or reflex voiding.2 In MS, the central nervous system (CNS) lesions disrupt the nerve pathways between the pons and the sacral nerves that result in a neurogenic bladder. This manifests in the form of urinary symptoms such as increased urgency, frequency, urge incontinence, voiding dysfunction and urinary retention.3 4 These patients may require long-term urethral or SPC.5 Bladder stones are a well-known complication of an indwelling catheter. Roughly 36% of patients with a catheter in situ have bladder stones within an 8-year life span. This is often due to catheter encrustation; the catheter is a foreign body and therefore bacteria initiate the formation of a biofilm, which is composed of bacterial glycocalyces and host proteins.6
VVF is the most common type of urogenital fistula and is a known complication of gynaecological, urological or other pelvic surgeries.7 Other causes of VVF include postradiation therapy, locally advanced malignancies, urological or gynaecological instrumentation, including percutaneous procedure, retroperitoneal, vascular or pelvic surgery, infectious and inflammatory diseases, foreign bodies (including neglected pessaries), sexual trauma, vaginal laser procedures and external violence.8
However, it is very rare for VVF to develop from pressure necrosis from a large vesical calculus(figure 7). Looking through the published case reports, there has been no similar case in the UK or any of the western countries. There was one case of bladder stone associated with VVF and two with rectourethral fistula, reported by Mukerji et al in 1970 from India.9 A recent case report of a 56-year-old woman presenting with dysuria and urinary incontinence in Indonesia was reported by Francisca et al. On evaluation, she was noted to have a fistula and stone. USG of the urinary tract revealed a hyperechoic shadow in the vesica-urinary and an X-ray KUB showed a radioopaque shadow in the pelvis. In this case, the stone was removed through an open cystolithotomy and a fistula repair was performed.10
Pathophysiology of fistulation and stone migration (figure created by authors).
Our case was unique in the fact that it is the first case of a VVF secondary to a vesicle calculus in a patient with MS. This case is also unique in the fact that the bladder stone migrated into the vagina due to the VVF. The VVF defect could not be closed in the same setting because of the inflamed bladder mucosa and the large size of the defect.
It is intriguing to think as to why the bladder stone was missed long enough for it to erode into the vagina. Retrospectively it can be concluded that the patients’ urinary symptoms could have been investigated with imaging at an early stage or a timely referral to urology could have prevented this complication.
Patient’s perspective
We understand that this complication of a VVF forming due to a long standing bladder stone is extremely rare. We are in agreement that conservative management of the VVF is the better option given the size of the VVF and the general health condition.
Learning points
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Bladder stones are a common phenomenon in a neurogenic bladder and can present with variety of symptoms.
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It is important to recognise that indwelling catheters can become encrusted increasing the incidence of bladder stones that can present with recurrent catheter blockage and leak.
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If left untreated bladder stones can lead to urinary tract infection, urosepsis, upper urinary tract compromise resulting in renal failure and on very rare occasion can lead to pressure necrosis of bladder wall leading to vesicovaginal fistula.
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This case report highlights the importance of early referral of bladder stones to urology for appropriate management and follow-up.
Ethics statements
Patient consent for publication
Footnotes
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Twitter @iamdrparag, @Mehwash_Nadeem
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Contributors MN proposed, contributed and reviewed the manuscript. VS produced the first draft, obtained the necessary consent. PS contributed, revised and prepared the final draft of the manuscript.
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Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
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Case reports provide a valuable learning resource for the scientific community and can indicate areas of interest for future research. They should not be used in isolation to guide treatment choices or public health policy.
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Competing interests None declared.
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Provenance and peer review Not commissioned; externally peer reviewed.
- © BMJ Publishing Group Limited 2022. No commercial re-use. See rights and permissions. Published by BMJ.
References
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