Enterovesical fistula is an abnormal communication between the intestine and the bladder and may markedly affect patients quality of life [1] . Historically, enterovesical fistula was described by Rufus of Ephesus as early as the second century AD [2] . It is an uncommon disease which occurs most frequently in advanced stage malignancies or from traumatic or iatrogenic injuries [1] . Based on the bowel segment involved, it can be divided into colovesical (the commonest form), rectovesical, ileovesical and appendicovesical fistula [3] . Diverticulitis is the most common aetiology which accounts for 50% - 70% of cases [3] .

Although the pathology is usually of intestinal origin, the majority of problems are referred to the urologist because of urological symptoms [4] . Pneumaturia, fecaluria and recurrent urinary tract infections are common methods of presentation in enterovesical fistula [5] [6] . Diagnosis of this disease is sometimes challenging and patients may be monitored for months before recognition of this disease [3] .

Myomectomy involves surgical removal of uterine fibroid. Several complications could follow this procedure but enterovesical fistula is an uncommon com- plication. Our aim is to present a case of enterovesical fistula following myomectomy.

She is a 33-year-old nullipara who presented at the National Obstetric Fistula Centre, Abakaliki, Ebonyi State, South-Eastern Nigeria with a history of fecaluria and pneumaturia which started a year after myomectomy. She had myomectomy for symptomatic uterine fibroid in a tertiary health facility in Nigeria and subsequently presented to our health facility three years later with these symptoms. She also gave a history of associated lower abdominal pain. There were no other co-morbidities.

On examination, patient was pale (packed cell volume was 29%). Pfannensteil scar was noted. The uterus was eighteen-week size. Feculent fluid was obtained on urethral catheterization. Based on the above findings, an assessment of enterovesical fistula was made. She was placed on haematinics and packed cell volume appreciated to 31% after three weeks.

Cystogram done for her showed leakage of contrast into the bowel. There was no leakage into the uterus. The diagnosis of enterovesical fistula was sustained. Abdominopelvic ultrasound done showed multiple uterine fibroid. Hysterosalpingogram showed that there was no spillage of contrast in both tubes.

Patient was counselled and subsequently had laparatomy for repair of enterovesical fistula after adequate bowel preparation. Findings at surgery were extensive adhesion of the gut, bladder, uterus and anterior abdominal wall. Enterovesical fistula was demonstrated and uterine myoma was also noted. Adhesiolysis was done. The bladder, bowels and uterus were separated. The bowel and bladder were repaired separately in two layers with absorbable suture. The peritoneum was irrigated with normal saline. Rectus sheath and abdomen were then closed. Patient was placed on analgesics and antibiotics in the postoperative period.

The intestinal origin of enterovesical fistula includes the sigmoid colon, rectum, ileum, descending colon, transverse colon and ascending colon [5] . Majority of cases of colovesical fistula are from diverticular disease [6] . Other causes include colon cancer, crohn’s disease, surgeries and actinomycosis [5] [6] [7] [8] . It is less common in females because there is interposition of the female reproductive organs between the colon and the bladder [9] .

Enterovesical fistula is diagnosed primarily by clinical findings [5] . Presenting features include fecaluria, pneumaturia and recurrent urinary tract infection [5] [6] [7] . Other symptoms are dysuria, urinary frequency, haematuria, haematochezia, diarrhoea, alteration of bowel habit, urinary flow via the rectum and abdominal pain [5] [7] [10] . Our patient had fecaluria, pneumaturia and lower abdominal pain. Based on these findings, a clinical diagnosis of enterovesical fistula was made.

A high index of suspicion is required to prevent a delay in the diagnosis of this disease condition. As seen in this case report, diagnosis and surgical repair of enterovesical fistula was done three years after myomectomy. She made several hospital visits in other health facilities with these complaints but the diagnosis was not made. Being a rare complication of myomectomy, a surgeon may not entertain this diagnosis early enough, unless from a high index of suspicion.

Imaging studies for enterovesical fistula includes cystography, computerized tomography, ultrasonography and magnetic resonance imaging [1] [3] [11] . The cystogram of our patient showed leakage of contrast into the bowel which was indicative of enterovesical fistula.

Treatment of enterovesical fistula can be conservative or surgical. Non operative management of enterovesical fistula may be an option in non toxic, minimally symptomatic patients with non malignant disease [1] . Operative management of enterovesical fistula is dependent on the aetiology, site of the bowel lesion, and patients preoperative status [1] . Our patient had surgical repair of enterovesical fistula and was lost to follow up.

Enterovesical fistula is an uncommon but possible complication of myomectomy. Diagnosis can be made clinically. However, a high index of suspicion is needed to prevent delay in this disease condition. Typical symptoms of this disease are fecaluria and pneumaturia.

Consent was obtained from the patient for publication of this article.

Ekwedigwe, K.C., Sunday-Adeoye, I., Lengman, S., Isikhuemen, M.E., Daniyan, A.B.C., Yakubu, E.N., Eliboh, M.O. and Uguru, I.E.A. (2017) Enterovesical Fistula Complicating Myomectomy: A Case Report. Open Journal of Urology, 7, 75-78. https://doi.org/10.4236/oju.2017.74010