An intestinal polyp is any mass of tissue that arises from the bowel wall and protrudes into the lumen. Most are asymptomatic except for minor bleeding, which is usually occult. The main concern is malignant transformation; most colon cancers arise in a previously benign adenomatous polyp. Diagnosis is by endoscopy. Treatment is endoscopic removal.
(See also the American College of Gastroenterology's practice guidelines for diagnosis, treatment, and surveillance for patients with colorectal polyps.)
Polyps may be sessile or pedunculated and vary considerably in size. Incidence of polyps ranges from 7 to 50%; the higher figure includes very small polyps (usually hyperplastic polyps or adenomas) found at autopsy. Polyps, often multiple, occur most commonly in the rectum and sigmoid and decrease in frequency toward the cecum. Multiple polyps may represent familial adenomatous polyposis (see Tumors of the GI Tract: Familial Adenomatous Polyposis). About 25% of patients with cancer of the large bowel also have satellite adenomatous polyps.
Adenomatous (neoplastic) polyps are of greatest concern. Such lesions are classified histologically as tubular adenomas, tubulovillous adenomas (villoglandular polyps), or villous adenomas. The likelihood of cancer in an adenomatous polyp at the time of discovery is related to size, histologic type, and degree of dysplasia; a 1.5-cm tubular adenoma has a 2% risk of containing a cancer vs a 35% risk in 3-cm villous adenomas. Serrated adenomas, a somewhat more aggressive type of adenoma, may develop from hyperplastic polyps.
Nonadenomatous (nonneoplastic) polyps include hyperplastic polyps, hamartomas (see Tumors of the GI Tract: Peutz-Jeghers Syndrome), juvenile polyps, pseudopolyps, lipomas, leiomyomas, and other rarer tumors. Juvenile polyps occur in children, typically outgrow their blood supply, and autoamputate some time during or after puberty. Treatment is required only for uncontrollable bleeding or intussusception. Inflammatory polyps and pseudopolyps occur in chronic ulcerative colitis and in Crohn disease of the colon. Multiple juvenile polyps (but not sporadic ones) convey an increased cancer risk. The specific number of polyps resulting in increased risk is not known.
Symptoms and Signs
Most polyps are asymptomatic. Rectal bleeding, usually occult and rarely massive, is the most frequent complaint. Cramps, abdominal pain, or obstruction may occur with a large lesion. Rectal polyps may be palpable by digital examination. Occasionally, a polyp on a long pedicle may prolapse through the anus. Large villous adenomas may rarely cause watery diarrhea that may result in hypokalemia.
Diagnosis is usually made by colonoscopy. Barium enema, particularly double-contrast examination, is effective, but colonoscopy is preferred because polyps also may be removed during that procedure. Because rectal polyps are often multiple and may coexist with cancer, complete colonoscopy to the cecum is mandatory even if a distal lesion is found by flexible sigmoidoscopy.
Polyps should be removed completely with a snare or electrosurgical biopsy forceps during total colonoscopy; complete excision is particularly important for large villous adenomas, which have a high potential for cancer. If colonoscopic removal is unsuccessful, laparotomy should be done. Tattooing the distal margin of the polyp with India ink helps the surgeon locate the polyp during laparotomy.
Subsequent treatment depends on the histology of the polyp. If dysplastic epithelium does not invade the muscularis mucosa, the line of resection in the polyp's stalk is clear, and the lesion is well differentiated, endoscopic excision and close endoscopic follow-up should suffice. Patients with deeper invasion, an unclear resection line, or a poorly differentiated lesion should have segmental resection of the colon. Because invasion through the muscularis mucosa provides access to lymphatics and increases the potential for lymph node metastasis, such patients should have further evaluation (as in colon cancer—see Tumors of the GI Tract: Colorectal Cancer).
The scheduling of follow-up examinations after polypectomy is controversial. Most authorities recommend total colonoscopy annually for 2 yr (or barium enema if total colonoscopy is impossible), with removal of newly discovered lesions. If 2 annual examinations are negative for new lesions, colonoscopy is recommended every 2 to 3 yr. Current cost containment recommendations extend the interval between colonoscopies to 5 yr or longer.
Aspirin and COX-2 inhibitors may help prevent formation of new polyps in patients with polyps or colon cancer.
(See also the Cochrane review abstracts: dietary fibre, calcium supplementation, and aspirin and NSAIDs for the prevention of colorectal adenomas and carcinomas.)
Last full review/revision October 2012 by Elliot M. Livstone, MD