Adenocarcinoma following urinary diversion.
|Abstract:||The use of bowel segments in urinary diversions has been associated with an increased risk of neoplasia. This report describes three cases of intestinal adenocarcinoma following urinary diversion. In the first case, a 73-year-old woman developed moderately-differentiated colonic adenocarcinoma in her Indiana pouch 10.5 years after cystectomy. The second case involved a 77-year-old man with well-differentiated adenocarcinoma in his Indiana pouch 9 years after radical cystoprostatectomy and en bloc urethrectomy. The third case involved a 38-year-old man with moderately-differentiated adenocarcinoma arising in his ileal conduit 33 years after the creation of the conduit. These cases highlight the diagnostic signs of adenocarcinoma arising in urinary diversions and emphasize the importance of lifelong surveillance in these patients.|
|Article Type:||Clinical report|
(Complications and side effects)
Adenocarcinoma (Care and treatment)
Adenocarcinoma (Case studies)
Jian, Peter Yicum
Ro, Jae Y.
Zhai, Qihui "Jim"
Lerner, Seth P.
|Publication:||Name: Canadian Urological Association Journal (CUAJ) Publisher: Canadian Urological Association Audience: Academic Format: Magazine/Journal Subject: Health Copyright: COPYRIGHT 2012 Canadian Urological Association ISSN: 1911-6470|
|Issue:||Date: April 1, 2012 Source Volume: 6 Source Issue: 2|
|Geographic:||Geographic Scope: Canada Geographic Code: 1CANA Canada|
Author(s): Peter Yicum Jian, MD, Guilherme Godoy, MD, Michael Coburn,
MD, Garrett Lynch, MD, Jae Y. Ro, MD, Qihui "Jim" Zhai, MD,
Michiya Nishino, MD, Seth P. Lerner, MD, FACS
Exposure of intestinal mucosa to urine has been associated with an increased risk of tumorigenesis.[sup.1] Although the pathogenesis of these tumours has not been well-established, many possible explanations exist. First, in patients with ureterosigmoidostomy, the blending of fecal and urinary materials is thought to increase the production of nitrosamines at the site of the uretero-colonic anastamosis.[sup.2] Second, in the absence of fecal and urinary blending, chronic inflammation, irritation, presence of stones and elevation of a variety of substances have been implicated in carcinogenesis within the intestinal segment.[sup.1] The carcinogenic substances currently being investigated include nitrosamine, reactive oxygen species, epidermal growth factor, transforming growth factor, cyclo-oxygenase, mucin and ornithine transcarbamylase.[sup.1] Many of these substances have also been suggested as potential causes of adenocarcinoma in not only Indiana pouches and ileal conduits, but also in neobladders. In the absence of mixing of the urinary and fecal streams, there does not appear to be any increased risk per se in a urinary diversion beyond that inherent in the bowel segment in a non-diverted patient. Third, de novo adenocarcinoma may develop in any bowel segment, including the portion used in urinary diversions.[sup.3] Thus, the origin of these tumours is likely to be multifactorial. The following uncommon presentations of adenocarcinoma following urinary diversion surgery emphasize the diverse circumstances in which these malignancies can develop.
A 73-year-old female with a history of recurrent non-muscle invasive urothelial carcinoma of the bladder came to urology clinic. Her chief complaint was hematuria 10.5 years after radical cystectomy, extended lymph node dissection and continent urinary diversion with an Indiana pouch. Final pathology of the cystectomy showed a pTaG2_urothelial carcinoma of the bladder and carcinoma in situ. She had been in continuous follow-up postoperatively without evidence of recurrence. Magnetic resonance imaging (MRI) of the abdomen demonstrated a solid 2.5-cm mass localized in the posterior-inferior wall inside the Indiana pouch (Fig. 1, panel A). Endoscopy of the pouch revealed a sessile mucinous mass, and biopsy of the lesion was consistent with adenocarcinoma of the colon. Colonoscopy did not show any primary lesions in the large bowel, and an extensive metastatic workup was negative. The Indiana pouch was resected en bloc with the mesentery which was equivalent to a right hemicolectomy, which is standard of care. The urinary diversion was replaced by an ileal conduit.
The pouchectomy specimen contained a 3.5 x 2.5 cm, firm, off-white, polypoid lesion in a segment of large bowel (Fig. 1, panel B). The lesion was located 2.5 cm and 3 cm from each of the inner ureteral orifices and 4 cm from the ileocecal valve. Histological examination of the tumour revealed moderately-differentiated colonic adenocarcinoma invading into the submucosa (Fig. 1, panel C). No lymphovascular invasion was detected. Nineteen benign lymph nodes were identified, and resection margins were free of tumour. The final stage of the adenocarcinoma was T1, N0, M0. The patient recovered uneventfully from surgery, and is alive and free of disease 3 years after surgery.
A 77-year-old male with a history of recurrent non-muscle invasive urothelial carcinoma of the bladder came to the urology clinic. His chief complaint was hematuria 9 years after treatment with radical cystoprostatectomy, en bloc urethrectomy, extended lymph node dissection and continent urinary diversion with an Indiana pouch. His final pathology showed carcinoma in situ of the bladder and prostatic urethra. He had been in continuous follow-up postoperatively without evidence of recurrence. Endoscopy of the pouch revealed a sessile mass, and biopsy of the lesion was consistent with adenocarcinoma of the colon. The Indiana pouch was resected, and the urinary diversion was replaced by an ileal conduit, similar to the first case.
The pouchectomy specimen contained a 3.0 x 2.3 cm, firm, fungating mass in the large bowel segment (Fig. 2, panel A). This mass was located 3.1 cm from the right ureter, 5.5 cm from the left ureter and 12 cm from the ileocecal valve. Histological examination of the tumour revealed a well-differentiated colonic adenocarcinoma invading into the superficial muscularis propria (Fig. 2, panel B). No lymphovascular invasion was detected. Ten benign lymph nodes were identified, and resection margins were free of tumour. The final stage of the adenocarcinoma was T2, N0, M0. The patient died 3 months after surgery from infection-related complications associated with a fistula of the small bowel.
A 38 year-old male with a history of rhabdomyosarcoma of the bladder came to the urology clinic with a 3-week history of progressive episodic lower abdominal pain and hematuria. His surgical history included cystectomy and urinary diversion with an ileal conduit at the age of 5 years. His medical history included chronic nephrolithiasis, urinary tract infections and three episodes of small bowel obstruction managed with extensive enterectomy. A computed tomography (CT) scan and renal ultrasound revealed severe left hydronephrosis and hydroureter without suspicious mass or renal calculi. Cystoscopy showed two masses within the ileal conduit, and biopsy of the tumours showed intestinal tubular adenoma with high-grade dysplasia and focal intramucosal adenocarcinoma. The patient underwent left nephrectomy, right hemicolectomy and complete resection of his ileal conduit. A right hemicolectomy was chosen because it is the standard of care for adenocarcinoma of the distal ileum. A segment of the transverse colon was used to construct the urinary diversion because only 120 cm of the small bowel remained after the patient's previous operations.
The resected ileal conduit contained a fungating lesion measuring 2.5 cm in greatest dimension located 0.3 cm and 2.5 cm, respectively from the ureteral orifices. Histological examination of the tumour revealed moderately-differentiated adenocarcinoma invading into the submucosa and muscularis propria (Fig. 3). Vascular and ureteral margins were free of tumour, and no lymphovascular invasion was identified. Twenty-nine benign lymph nodes were identified, and no evidence of tumour was seen in the left nephrectomy and right hemicolectomy specimens. The final stage of the disease was T2, N0, M0.
In case reports and experimental studies, investigators have long hypothesized about the association between the presence of urinary diversion and malignancies in the intestinal tract. The three cases emphasize the diagnostic insights and treatment options associated with adenocarcinoma arising in the urinary diversions and underline the importance of lifelong surveillance in these patients.
In Cases 1 and 2, the patients' adenocarcinomas arose in Indiana pouches. Seven cases have been described in the literature (Table 1, Table 2).[sup.3]-[sup.19] The most common initial symptom is gross hematuria. Other signs and symptoms include particulate discharge from the pouch, stones in the pouch, difficulty with catheterization, pouch distention and overflow incontinence. The treatment of choice is complete resection of the Indiana pouch, equivalent to a right hemicolectomy, which is the standard of care for adenocarcinomas arising in the right colon. Case 3 is an example of an adenocarcinoma arising in an ileal conduit. Again, the main presenting symptom was gross hematuria.[sup.20]-[sup.22] The length of time between the creation of the ileal conduit and tumour detection as reported in the literature ranged from 14 to 30 years.
Adenocarcinomas can arise in a variety of circumstances in which intestinal segments are used for urinary diversions. Importantly, latent tumours can arise in a defunctionalized ureterosigmoidostomy, as well as in isolated portions of ileum or colon used for the urinary diversion. Therefore, patients undergoing any type of urinary diversion involving intestinal mucosa should undergo close surveillance following surgery. In patients with colonic reservoirs, consideration should be given to pouchoscopy along with routine colonoscopy when screening for colon cancer. Gross hematuria is the most common symptom and should always be actively investigated. Other signs and symptoms, such as particulate discharge, stones in the pouch, difficulty with catheterization, pouch distention, overflow incontinence, rectal bleeding, changes in bowel habits and abdominal pain should not be overlooked. Detection of localized cancer allows for primary resection of the bowel segment and mesentery, which should be curative.
The authors would like to thank Dr. Mukul K. Divatia for coordinating retrieval of pathology images.
Competing interests: None declared.
This paper has been peer-reviewed.
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Figures and Tables
Fig. 1.: A. Post-gadolinium T2 weighted magnetic resonance imaging of the abdomen in case 1 demonstrates a solid 2.5 cm mass in the posterior-inferior wall inside the Indiana pouch as indicated by the arrow. B. The resected Indiana pouch contains a 3.5 x 2.5 cm, firm, off-white, polypoid lesion in a segment of the large bowel. C. Histological examination of the tumor reveals moderately differentiated colonic adenocarcinoma that invades into the submucosa. (Hemotoxin & Eosin, low power magnification). [Figure omitted]
Fig. 2.: A. The resected Indiana pouch in case 2 contains a 3.0 x 2.3 cm, firm, fungating mass in a segment of the large bowel. B. Histological examination of the tumour under high power magnification reveals well differentiated colonic adenocarcinoma that invades into the superficial muscularis propria. (Hemotoxin & Eosin, low power magnification). [Figure omitted]
Fig. 3.: Histologic examination of resected ileal conduit in case 3 demonstrates moderately-differentiated adenocarcinoma that invades into the muscularis propria. (Hemotoxin & Eosin, low power magnification). [Figure omitted]
Table 1.: Review of clinical characteristics of reported colonic adenocarcinoma arising in Indiana pouch [Table omitted]
Table 2.: Review of pathological characteristics and outcomes of reported colonic adenocarcinoma arising in Indiana pouch [Table omitted]
 Scott Department of Urology, Baylor College of Medicine, Houston, TX;
 Margaret M. and Albert B. Alkek Department of Medicine, Baylor College of Medicine, Houston, TX;
 Department of Pathology, The Methodist Hospital, Houston, TX;
 Department of Pathology, University of Cincinnati, Greater Cincinnati Pathologists, Inc. Cincinnati, OH;
 Medical Scientist Training Program, Baylor College of Medicine, Houston, TX
Correspondence: Dr. Seth P. Lerner, Professor of Urology, Beth and Dave Swalm Chair of Urologic Oncology, Scott Department of Urology, Baylor College of Medicine, 6620 Main, Suite 1325, Houston, Texas 77030; fax: 713-798-5553; email@example.com
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