Metachronous, colitis-associated rectal cancer that developed after sporadic adenocarcinoma in an adenoma in a patient with longstanding Crohn’s disease: a case report
- Hiroshi Takeyama1,
- Tsunekazu Mizushima1Email author,
- Kiyokazu Nakajima1,
- Mamoru Uemura1,
- Naotsugu Haraguchi1,
- Junichi Nishimura1,
- Taishi Hata1,
- Ichiro Takemasa1,
- Hirofumi Yamamoto1,
- Yuichiro Doki1 and
- Masaki Mori1
© Takeyama et al.; licensee BioMed Central Ltd. 2013
Received: 30 April 2013
Accepted: 9 November 2013
Published: 19 November 2013
Colorectal cancer associated with Crohn’s disease (CD) is increasing in proportion to the number of patients with CD in Japan. There are two subtypes of colorectal cancer with CD: sporadic cancer and colitis-associated cancer. Early diagnosis of colitis-associated cancer is sometimes difficult; when colorectal cancer is found in patients with CD, both colitis-associated cancer and sporadic cancer should be kept in mind. Here, we describe a case of metachronous, colitis-associated rectal cancer that developed after the complete resection of an adenoma that became a sporadic adenocarcinoma in a patient with longstanding CD. To the best of our knowledge, this is the first report of colitis-associated cancer in a patient with CD after removal of a sporadic cancer.
We describe a 51-year old man with CD who had difficulty in defecation. A rectal polyp was detected and a transanal resection of the polyp was performed. A histopathological examination showed an adenoma with sporadic adenocarcinoma. After three years, a follow-up colonoscopy revealed a reddish, elevated lesion in the patient’s rectum. A colonoscopic biopsy showed a signet ring cell carcinoma. We performed an abdominoperineal resection of the rectum and a bilateral pelvic lymph node dissection. A histopathological examination revealed a mucinous adenocarcinoma with signet ring cell carcinoma and lymph node metastasis. The patient received adjuvant chemotherapy with oral uracil 224 mg combined with tegafur 100 mg plus leucovorin. No signs of recurrence were noted at a follow-up 18 months after the third surgery and 60 months after the second surgery.
KeywordsColitis-associated cancer Crohn’s disease Sporadic cancer
- H & E:
Hematoxylin and eosin
Inflammatory bowel disease
Colorectal carcinoma (CRC) is a serious complication of inflammatory bowel disease (IBD). CRC accounts for approximately 15% of all deaths associated with IBD . CRC has been thoroughly studied in conjunction with ulcerative colitis (UC) , but CRC is not well understood in conjunction with Crohn’s disease (CD). Several reports have described an increased incidence of CRC in CD [3–5]. However, relatively few studies have focused on CRCs in CD. No well-defined risk factors have been associated with the development of CRC in CD. Moreover, we lack clear recommendations for surveillance and surgical strategies for addressing CRC in CD . CRC in patients with IBD can be classified into two subtypes, colitis-associated cancer and sporadic cancer, with different pathogenic and clinicopathological characteristics . Few reports have precisely described each type of CRC in CD. To the best of our knowledge, no report has described metachronous sporadic and colitis-associated cancers in the same patient. This study is the first to report colitis-associated adenocarcinoma in a patient with CD after the removal of a sporadic adenocarcinoma.
The patient was a 51-year old man with CD. He was initially diagnosed with CD at 23 years old. He had undergone ileocecal resection, owing to a stricture of the terminal ileum, at 36 years old, and the residual small intestine was 230 cm long. After the initial operation, he was prescribed 5-aminosalicylic acid and home parenteral nutrition. He did not accept a recommended colonoscopy examination, owing to anal pain.
Postoperatively, the patient received adjuvant chemotherapy with 224 mg oral uracil combined with100 mg tegafur plus leucovorin for 6 months. The patient has continued with regular follow-ups over the last 18 months after the third surgery and over the last 60 months after the second surgery. He has also undergone regular examinations. A regular colonoscopy examination was performed every 6 months, and no relapse of colonic inflammation or dysplasia was detected.
CRC accounts for approximately 15% of all deaths in patients with IBD [6, 7]. The risk of CRC for patients with IBD increases by 0.5% to 1% yearly from 8 to 10 years after the IBD diagnosis. A meta-analysis of published studies that focused on the CRC risk in UC showed that the risk of CRC for patients with colitis was 2% at 10 years, 8% at 20 years, and 18% after 30 years of colitis . Previously, CD was not considered a risk factor for CRC; however, recent studies have shown that the CRC risk in patients with colonic CD is similar to that of patients with UC [7, 9].
In patients with IBD, CRC can take the form of sporadic cancer or colitis-associated cancer. In patients with UC who develop colitis-associated cancer, total proctocolectomy is the standard treatment; however, when sporadic cancer occurs, total proctocolectomy is not always necessary. In patients with CD, an indication for total proctocolectomy has been controversial. However, it was also reported that, when a diagnosis of colitis-associated cancer is known in advance of surgery, a total proctocolectomy should be seriously considered, to eliminate the risk of metachronous disease. In 44% of these patients, dysplasia occurred at a site remote from the site of the cancer . However, this patient had already undergone ileocecal resection and the residual small intestine was 230 cm long, resulting in intestinal failure syndrome requiring home parental nutrition. For these reasons, we chose abdominoperineal resection with colostomy, not total proctocolectomy with ileostomy, in order to preserve the colon and maintain absorption of water and electrolytes. After the last surgery, we conducted intensive cancer surveillance and neither a recurrence nor another lesion has been detected at this time.
However, the site of inflammation should be resected, owing to the risk of dysplasia. When the colon and rectum are preserved in surgery, a scheduled, annual surveillance with biopsies is strongly recommended . It is very important, when planning therapy and surveillance after surgery, to perform a differential diagnosis to distinguish between colitis-associated CRC and sporadic CRC. However, it is often difficult to achieve this differential diagnosis in patients with IBD, particularly before surgery [11, 12].
The American Gastroenterological Association and the British Society for Gastroenterology surveillance guidelines have recommended beginning surveillance after 8 to 10 years of disease in cases of CD or extensive UC, and after 15 to 20 years of disease in cases of left-sided UC [13–15]. However, the evidence on which this is based on is poor. It was reported that cancer has occurred in a substantial number of patients with IBD (17% to 28%) before the recommended time intervals for surveillance .
Clinically, endoscopic examination is the most useful screening method. However, even with endoscopic examination, it is often difficult to detect dysplastic changes. Colitis-associated dysplasia may show subtle macroscopic features that mimic a broad variety of lesions, ranging from inflammation to carcinoma. Previous reports have indicated that dysplastic lesions were not visible upon endoscopy in 50% to 80% of cases with colitis-associated cancers . Conversely, sporadic cancer mainly develops from polyps that are on the pathway to becoming adenoma-carcinomas, and a polyp is easily detectable, even in a normal endoscopy examination. In contrast, the gross appearance of colitis-associated neoplasms varies from case to case, as the neoplasm develops from dysplasia to become a carcinoma. Dysplastic lesions may be irregularly delineated, plaque-like, irregularly elevated, or verrucous structures; therefore, they are difficult to identify with normal endoscopy .
This case should make surgeons and endoscopists aware of the possibility that patients with CD may develop either colitis-associated cancer or sporadic cancer. This report should alert surgeons and endoscopists to look for colitis-associated cancers that are in a precancerous or early stage. In this case study, although we performed annual colonoscopic surveillance, we did not detect the second lesion, the colitis-associated cancer, until it reached an advanced cancerous stage. Early detection is highly important for avoiding surgeries, including colectomy or proctectomy. However, it is often difficult to detect colitis-associated cancers in dysplastic, precancerous, or early stages. We need further investigation to discover novel biomarkers that make it possible to detect cancer in blood samples or biopsies.
To the best of our knowledge, this is the first case report of a metachronous colitis-associated rectal cancer that arose in a patient with CD after removal of a sporadic cancer. This case emphasized the importance for clinicians to bear in mind the possibilities of both sporadic cancer and colitis-associated cancer when following-up patients with CD. It is also important to consider surgical therapy and surveillance after surgery, and to perform a differential diagnosis to distinguish between colitis-associated cancer and sporadic cancer. CRC associated with CD remains a rare occurrence, and there is no defined surveillance strategy. However, patients with longstanding CD should receive cancer surveillance as frequently as do patients with UC.
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the editor-in-chief of this journal.
- Munkholm P: Review article: the incidence and prevalence of colorectal cancer in inflammatory bowel disease. Aliment Pharmacol Ther 2003,18(2):1–5.PubMedView Article
- Maratka Z, Nedbal J, Kocianova J, Havelka J, Kudrmann J, Hendl J: Incidence of colorectal cancer in proctocolitis: a retrospective study of 959 cases over 40 years. Gut 1985, 26:43–49.PubMedView Article
- Averboukh F, Ziv Y, Kariv Y, Zmora O, Dotan I, Klausner JM, Rabau M, Tulchinsky H: Colorectal carcinoma in inflammatory bowel disease: a comparison between Crohn’s and ulcerative colitis. Colorectal Dis 2011, 13:1230–1235.PubMedView Article
- Mpofu C, Watson AJ, Rhodes JM: Strategies for detecting colon cancer and/or dysplasia in patients with inflammatory bowel disease. Cochrane Database Syst Rev 2004, 2:CD000279.PubMed
- Ruffolo C, Scarpa M, Polese L, D’Amico FE, Boetto R, Pozza A, D’lnca R, Checchin D, Sturniolo GC, Bassi N, Angriman I: Clinical presentation and diagnosis of intestinal adenocarcinoma in Crohn’s disease: analysis of clinical predictors and of the life-time risk. J Gastrointest Surg 2010, 14:1746–1751.PubMedView Article
- Itzkowitz SH, Harpaz N: Diagnosis and management of dysplasia in patients with inflammatory bowel diseases. Gastroenterology 2004, 126:1634–1648.PubMedView Article
- Vagefi PA, Longo WE: Colorectal cancer in patients with inflammatory bowel disease. Clin Colorectal Cancer 2005, 4:313–319.PubMedView Article
- Eaden JA, Abrams KR, Mayberry JF: The risk of colorectal cancer in ulcerative colitis: a meta-analysis. Gut 2001, 48:526–535.PubMedView Article
- Bernstein CN, Blanchard JF, Kliewer E, Wajda A: Cancer risk in patients with inflammatory bowel disease: a population-based study. Cancer 2001, 91:854–862.PubMedView Article
- Kiran RP, Nisar PJ, Goldblum JR, Fazio VW, Remzi FH, Shen B, Lavery IC: Dysplasia associated with Crohn’s colitis: segmental colectomy or more extended resection? Ann Surg 2012, 256:221–226.PubMedView Article
- Nagasako K, Iizuka B, Ishii F, Miyazaki J, Fujimori T: Colonoscopic diagnosis of dysplasia and early cancer in longstanding colitis. J Gastroenterol 1995,30(8):36–39.PubMed
- Riddell RH, Goldman H, Ransohoff DF, Appelman HD, Fenoglio CM, Haggitt RC, Ahren C, Correa P, Hamilton SR, Morson BC, Sommers SC, Yardley JH: Dysplasia in inflammatory bowel disease: standardized classification with provisional clinical applications. Hum Pathol 1983, 14:931–968.PubMedView Article
- Eaden JA, Mayberry JF: Guidelines for screening and surveillance of asymptomatic colorectal cancer in patients with inflammatory bowel disease. Gut 2002,51(5):V10-V12.PubMedView Article
- Kornbluth A, Sachar DB: Ulcerative colitis practice guidelines in adults: American College of Gastroenterology, Practice Parameters Committee. Am J Gastroenterol 2010, 105:501–523. quiz 24PubMedView Article
- Winawer S, Fletcher R, Rex D, Bond J, Burt R, Ferrucci J, Ganiats T, Levin T, Woolf S, Johnson D, Kirk L, Litin S, Simmang C: Colorectal cancer screening and surveillance: clinical guidelines and rationale-update based on new evidence. Gastroenterology 2003, 124:544–560.PubMedView Article
- Lutgens MW, Vleggaar FP, Schipper ME, Stokkers PC, van der Woude CJ, Hommes DW, der Jong DJ, Dijkstra G, van Bodegraven AA, Oldenburg B, Samsom M: High frequency of early colorectal cancer in inflammatory bowel disease. Gut 2008, 57:1246–1251.PubMedView Article
- Bernstein CN, Shanahan F, Weinstein WM: Are we telling patients the truth about surveillance colonoscopy in ulcerative colitis? Lancet 1994, 343:71–74.PubMedView Article
- Neumann H, Vieth M, Langner C, Neurath MF, Mudter J: Cancer risk in IBD: how to diagnose and how to manage DALM and ALM. World J Gastroenterol 2011, 17:3184–3191.PubMed
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