- Case report
- Open Access
Asynchronous bilateral anastomosis site sigmoid colon cancer after ureterosigmoidostomy: a case report
© The Author(s). 2016
- Received: 9 February 2016
- Accepted: 28 June 2016
- Published: 7 July 2016
We present a case of asynchronously occurring adenocarcinomas 29 and 36 years after ureterosigmoidostomy for bladder cancer, respectively, at both anastomosis sites.
A colonoscopy that was performed on a 69-year-old man because of bloody stool and an elevated carcinoembryonic antigen (CEA) level revealed a polypoid lesion at the right ureterosigmoid anastomosis site 29 years after the patient’s ureterosigmoidostomy. Endoscopic resection was performed, and the lesion was diagnosed as adenocarcinoma. Seven years later (36 years after ureterosigmoidostomy), an elevated lesion was detected at the left ureterosigmoid anastomosis site by colonoscopy performed after detection of high CEA levels. Biopsy revealed an adenocarcinoma that was immunohistologically positive for CDX2; sigmoidectomy and ureterectomy were subsequently performed. The pathological diagnosis of the second tumor was adenocarcinoma arising in the ureterosigmoid anastomosis site and invading the left ureter.
Diligent long-term follow-up of patients who underwent ureterosigmoidostomy is essential.
- Colon cancer
Ureterosigmoidostomy used to be commonly performed to treat bladder cancer. However, the procedure was recently abandoned because of complications such as hyperchloremia, renal failure, urinary infection, and adenocarcinoma at the ureterosigmoid anastomosis site. We herein discuss a rare case of adenocarcinoma occurring at both ureterosigmoid anastomosis sites; one was detected 29 years after the procedure while the other was detected 36 years afterwards.
Ureterosigmoidostomy is a valid method for urinary diversion, as it is not associated with urinary incontinence. However, as exemplified by our patient, it is associated with urinary infection, renal dysfunction, acidosis from hyperchloremia, and colon cancer. In general, cancers that develop at the anastomosis site of a ureterosigmoidostomy tend to be one-sided. The patient in this case developed cancer at both anastomosis sites, which is rare. As such, this case highlights the importance of careful follow-up examinations after ureterosigmoidostomy. Because the pathological margin of the endoscopic resection was negative in our patient, the tumor at the left anastomosis site was deemed to have developed independently. The colon cancer was almost fatal for this patient.
Carcinoma at the site of the ureterocolic anastomosis was first reported in 1929 by Hammer . Kälble et al. reported that the occurrence of colon cancer in patients who had undergone ureterosigmoidostomy was eight to ten times higher than that in the general population . Urdaneta et al. calculated that the incidence of carcinoma after ureterosigmoidostomy was 13,300 per 100,000 cases . The mean lag period for the development of colon carcinoma after surgery was 8.7 and 21.4 years for patients who were over and under the age of 40 years at the time of the operation, respectively . The lesions were reported to be distal to the ureterosigmoidostomy site or involved the ureterocolonic junction . Histological evaluations revealed the growth to be malignant twice as often as it was benign, with adenocarcinoma of the colon being the most frequent diagnosis .
The treatment for such tumors has changed over time. In the 1970s, sigmoid colon cancer arising at anastomosis sites after ureterosigmoidostomy was managed by local extirpation of the lesion, with re-implantation of one or both ureters back into the sigmoid. Currently, the preferred treatment is either endoscopic resection or more extensive surgical resection of the involved bowel segment combined with cutaneous loop diversions for an obvious malignant lesion. In this case, the patient opted for endoscopic therapy, and the right-sided tumor at the anastomosis site was completely resected endoscopically. However, the left-sided tumor was suspected of being an infiltrating cancer; therefore, surgical resection was performed. Mortality from this type of carcinoma is reportedly 33 % in cases of late detection that exhibit prominent metastases to regional lymph nodes .
One theory to explain the carcinogenesis of colonic carcinoma after ureterosigmoidostomy is the formation of nitrosamines from bacterially reduced urinary nitrates and from endogenous amines in feces and urine [2, 7–9]. Another theory is the urine-stool admixture concept, which suggests that hydrolytic enzymes in the urine activate conjugated carcinogens in the stool. These carcinogens are most active at the junction of the two streams where the greatest concentration exists [5, 10, 11]. Other factors, such as chronic irritation of the bowel epithelium, instability of the borderline between the urothelium and colonic epithelium, metabolic changes, and the presence of a fresh colonic suture line may contribute to the induction of colon carcinoma after ureterosigmoidostomy [2, 10–13]. Any one of these factors may be responsible for tumor development in our patient. To detect cancer before it attains advanced stage, surveillance colonoscopy should be performed at regular intervals after ureterosigmoidostomy because cancer or polyps can develop as early as 2 years after surgery and progress over a few decades . The present case highlights the risk of cancer development after ureterosigmoidostomy as well as the importance of surveillance for early tumors. Based on the mechanism of tumorigenesis after ureterosigmoidostomy, tumors can develop either on the same or opposite side after resection, as in this case. Thus, follow-up examinations should be performed judiciously and at short intervals.
We presented a case of adenocarcinomas occurring at both anastomosis sites after ureterosigmoidostomy that were detected 29 and 36 years after the original surgery, respectively. Our experience suggests that adenocarcinoma at both anastomosis sites can occur asynchronously; therefore, long-term attentive follow-up is necessary.
CEA, carcinoembryonic antigen; CT, computed tomography
Other than the authors, no individuals or funding sources substantially contributed to the article, whether in the conception, design, acquisition of data, or analysis and interpretation of data. Furthermore, other than the authors, no individuals were involved in drafting the manuscript or revising it critically for important intellectual content.
This study was not supported by any external sources of funding.
Availability of data and materials
All the data on which the conclusions of this case report are based are included in this manuscript.
KA, SI, KK, JS, KO, KY, TN, TT, TK, KH, HY, HN, ES, JK, and TW were all involved in this report’s conception and coordination and helped to draft the manuscript. Additionally, all authors read and approved of the final version.
The authors declare that they have no competing interests.
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Written informed consent was obtained from the patient for the publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
Ethics approval and consent to participate
The requirement for institutional review board approval was waived because this case report did not contain the content of requirement to ethics approval.
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