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Colonic Polyps

para>JPS impose a higher risk of CRC, although juvenile polyps are not premalignant.  

DIAGNOSIS


HISTORY


  • Usually normal
  • Generally asymptomatic
  • Painless rectal bleeding, bright or dark red, mixed with stools, dripping, or on wiping
  • Diarrhea or mucous stool
  • Abdominal pain
  • Constipation
  • Chronic bleeding resulting in iron deficiency anemia
  • McKittrick-Wheelock syndrome; large hypersecretory rectosigmoid villous adenoma, resulting in persistent severe diarrhea, electrolyte disorder, dehydration, and prerenal acute renal failure
  • Social and family history

PHYSICAL EXAM


  • Usually normal
  • Rectal polyps noted as prolapsed or palpated on DRE
  • FOBT by DRE is less effective than FOBT by stool passed spontaneously.

DIAGNOSTIC TESTS & INTERPRETATION


Initial Tests (lab, imaging)
  • CBC; anemia with chronic bleeding
  • Basic metabolic panel; electrolyte disorder with hypersecretory adenomas
  • Fecal occult blood test (FOBT), an insensitive screening test, as small polyps don't usually bleed, includes:
    • Guaiac (gFOBT)-uses a chemical indicator with color change in presence of blood
    • Immunochemical (iFOBT or fecal immunochemical test [FIT])-uses antibodies against human hemoglobin
  • Stool DNA test is more sensitive and less specific than fecal immunochemical test (FIT).

Diagnostic Procedures/Other
  • Colonoscopy is the gold standard test for detection of polyps and polypectomy. Not a perfect screening test, with increased miss rate with right-sided colon polyps, smaller polyp size, low quality of colon prep, less endoscopist experience
  • Computed tomographic colonography (CTC) is less sensitive with flat polyps and requires excellent bowel preparation.
  • Double-contrast barium enema
  • Colon capsule endoscopy
  • Enhanced optical technologies can potentially differentiate between neoplastic and non-neoplastic colonic lesions (4)[A].
  • Enhanced optical technologies include:
    • Narrowed spectrum endoscopy (narrow-band imaging [NBI])
    • Image-enhanced endoscopy (i-scan)
    • Fujinon intelligent chromoendoscopy (FICE)
    • Confocal laser endomicroscopy (CLE)
  • Patients with >10 colorectal adenomas should get genetic testing for APC and MUTYH (5)[C].

Test Interpretation
  • Tubular adenoma
    • Gross: tend to be polypoid
    • Micro: dysplastic epithelium with a tubular architecture
  • Villous adenoma:
    • Gross: tend to be sessile
    • Micro: dysplastic epithelium with fine finger-like projections
  • Tubulovillous adenomas have a combination of tubular and villous architecture.
  • Hyperplastic polyps are composed of hyperplastic colonic mucosa.
  • Hamartomatous polyps include muscularis mucosa.
  • Juvenile polyp
    • Gross: pedunculated, smooth, red mass, 1 to 3 cm (2).

TREATMENT


SURGERY/OTHER PROCEDURES


  • Colonic polypectomy; diagnostic, therapeutic
  • Techniques are as follows:
    • Snare polypectomy with electrocautery for pedunculated polyps
    • Endoscopic mucosal resection for sessile polyps
    • Endoscopic submucosal dissection
  • Colorectal surgery; prophylactic in FAP and MAP and when there are numerous polyps or persistent bleeding (2,5)[C]:
    • Total colectomy ileorectal anastomosis
    • Proctocolectomy ileal pouch anal anatomosis
  • Chemoprevention: NSAIDs and calcium may reduce incidence and recurrence of polyps in patients with FAP and MAP (3)[A].

ONGOING CARE


FOLLOW-UP RECOMMENDATIONS


Follow-up colonoscopy in:  
  • 10 years if no polyps or distal small hyperplastic polyps (<10 mm) (1)[B]
  • 5 to 10 years if 1 to 2 small tubular adenomas (<10 mm) (1)[B]
  • 3 years if 3 to 10 adenomas if any polyp ≥6 mm (1)[B] or if all polyps <6 mm (1)[C]
  • <3 years if >10 adenomas (1)[B]
  • 3 years if one or more adenomas ≥10 mm (1)[A]
  • 3 years if one or more adenomas with villous features of any size or with HGD (1)[B]
  • 5 years if sessile serrated polyp(s) <10 mm with no dysplasia (1)[C]
  • 3 years if sessile serrated polyp(s) ≥10 mm or with dysplasia or traditional serrated adenoma (1)[C]
  • 1 year if serrated polyposis syndrome (1)[B]

Patient Monitoring
  • Colonoscopy for CRC screening starts at age 50 years and earlier for at-risk patients.
  • Stop screening if life expectancy is <10 years.
  • In CFAP and AFAP, screen for extracolonic manifestations: thyroid cancer, desmoid tumors, and gastroduodenal polyposis (every 6 months to 5 years) (5)[C]
  • In families, lifetime screening is indicated in mutation carriers (5)[C]:
    • In CFAP: with sigmoidoscopy or colonoscopy every 1 to 2 years starting at age of 10 to 11 years
    • In AFAP and MAP: with colonoscopy every 1 to 2 years starting at age of 18 to 20 years
  • After colorectal surgery, surveillance of the rectum (every 6 to 12 months) or pouch (every 6 months to 5 years) is indicated (5)[C].
  • First-degree relatives of patients with JPS require screening by colonoscopy and upper endoscopy after age 12 (2)[C].

DIET


Low-fat, high-fiber diet has been recommended but with insufficient evidence.  

PATIENT EDUCATION


Importance of colonoscopy as a screening tool for reduction of incidence of colorectal cancer  

PROGNOSIS


  • Regression or no change in size, more with small hyperplastic polyps and with patients on NSAIDs
  • Recurrence: Juvenile polyps recur in 45% of children with multiple polyps and 17% of children with solitary polyps (2).
  • Increase in size, more with large adenomas
  • Progression to cancer
  • Risk factors for colon cancer (6)[A]:
    • Polyp pathology
      • Adenomatous
      • Serrated
      • With high-grade dysplasia
      • With >25% villous histology
      • Polyp size >1 cm in diameter
      • Polyps located in proximal colon
      • More than three polyps
  • Recurrence rates <10% postpolypectomy

COMPLICATIONS


  • Polyps: progression to cancer
  • Polypectomy: bleeding 2-11%, perforation 0-1%, higher with endoscopic submucosal dissection
  • Colonoscopy: complications related to anesthesia and procedure itself

REFERENCES


11 Lieberman  DA, Rex  DK, Winawer  SJ, et al. Guidelines for colonoscopy surveillance after screening and polypectomy: a consensus update by the US Multi-Society Task Force on Colorectal Cancer. Gastroenterology.  2012;143(3):844-857.22 Thakkar  K, Fishman  DS, Gilger  MA. Colorectal polyps in childhood. Curr Opin Pediatr.  2012;24(5):632-637.33 Johnson  CC, Hayes  RB, Schoen  RE, et al. Non-steroidal anti-inflammatory drug use and colorectal polyps in the prostate, lung, colorectal, and ovarian cancer screening trial. Am J Gastroenterol.  2010;105(12):2646-2655.44 Wanders  LK, East  JE, Uitentuis  SE, et al. Diagnostic performance of narrowed spectrum endoscopy, autofluorescence imaging, and confocal laser endomicroscopy for optical diagnosis of colonic polyps: a meta-analysis. Lancet Oncol.  2013;14(13):1337-1347.55 Stoffel  EM, Mangu  PB, Limburg  PJ. Hereditary colorectal cancer syndromes: American Society of Clinical Oncology clinical practice guideline endorsement of the familial risk-colorectal cancer: European Society for Medical Oncology clinical practice guidelines. J Oncol Pract.  2015;11(3):e437-e441.66 Gao  Q, Tsoi  KK, Hirai  HW, et al. Serrated polyps and the risk of synchronous colorectal advanced neoplasia: a systematic review and meta-analysis. Am J Gastroenterol.  2015;110(4):501-509.

ADDITIONAL READING


  • Ashraf  I, Paracha  SR, Arif  M, et al. Digital rectal examination versus spontaneous passage of stool for fecal occult blood testing. South Med J.  2012;105(7):357-361.
  • Brenner  H, Hoffmeister  M, Arndt  V, et al. Protection from right- and left-sided colorectal neoplasms after colonoscopy: population-based study. J Natl Cancer Inst.  2010;102(2):89-95.
  • Cooper  K, Squires  H, Carroll  C, et al. Chemoprevention of colorectal cancer: systematic review and economic evaluation. Health Technol Assess.  2010;14(32):1-206.
  • Farraye  FA, Odze  RD, Eaden  J, et al. AGA medical position statement on the diagnosis and management of colorectal neoplasia in inflammatory bowel disease. Gastroenterology.  2010;138(2):738-745.
  • Imperiale  TF, Ransohoff  DF, Itzkowitz  SH, et al. Multitarget stool DNA testing for colorectal-cancer screening. N Engl J Med.  2014;370(14):1287-1297.
  • Lee  BG, Shin  SH, Lee  YA, et al. Juvenile polyp and colonoscopic polypectomy in childhood. Pediatr Gastroenterol Hepatol Nutr.  2012;15(4):250-255.
  • Sonnenberg  A, Genta  RM. Low prevalence of colon polyps in chronic inflammatory conditions of the colon. Am J Gastroenterol.  2015;110(7):1056-1061.
  • Summers  RM. Polyp size measurement at CT colonography: what do we know and what do we need to know? Radiology.  2010;255(3):707-720.

SEE ALSO


Colorectal Cancer  

CODES


ICD10


  • K63.5 Polyp of colon
  • D12.6 Benign neoplasm of colon, unspecified
  • K51.40 Inflammatory polyps of colon without complications
  • D12.5 Benign neoplasm of sigmoid colon
  • D12.2 Benign neoplasm of ascending colon
  • D12.3 Benign neoplasm of transverse colon
  • D12.4 Benign neoplasm of descending colon
  • D12.0 Benign neoplasm of cecum
  • D12.1 Benign neoplasm of appendix

ICD9


211.3 Benign neoplasm of colon  

SNOMED


  • 68496003 Polyp of colon (disorder)
  • 428054006 Adenomatous polyp of colon
  • 13025001 Pseudopolyposis of colon
  • 72900001 Familial multiple polyposis syndrome (disorder)
  • 428472008 Polyp of sigmoid colon (disorder)
  • 309084001 Villous adenoma of colon

CLINICAL PEARLS


  • Progression from normal mucosa to polyp to carcinoma is a sequence that takes years to develop.
  • Colonoscopy is the gold standard tool for diagnosis of polyps and reduction of CRC incidence.
  • Small hyperplastic polyps should be biopsied to differentiate adenomatous and serrated polyps.
  • Use of NSAIDs and calcium is associated with decreased incidence and recurrence of polyps.
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