Diagnosis and Management of Gastrointestinal Polyps:Pediatric Considerations

Gastroenterology Nursing

Volumn 29, Issue 1, 2006, Pages 16-22

  Attard, Thomas M ^a   Young, Rosemary J ^a  

^a UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; AGE; CHILD; COLON POLYPOSIS; COLON RESECTION; COLONOSCOPY; FEMALE; GASTROINTESTINAL POLYPOSIS; GASTROINTESTINAL TUMOR; GENETIC COUNSELING; GENETIC PREDISPOSITION; GENETICS; HUMAN; IMMUNOHISTOCHEMISTRY; INTESTINE POLYP; MALE; METHODOLOGY; MONITORING; NEEDLE BIOPSY; PEDIATRICS; PEDIGREE; PRESCHOOL CHILD; PROGNOSIS; REVIEW; RISK ASSESSMENT;

ADENOMATOUS POLYPOSIS COLI; ADOLESCENT; AGE FACTORS; BIOPSY, NEEDLE; CHILD; CHILD, PRESCHOOL; COLECTOMY; COLONOSCOPY; FEMALE; GASTROINTESTINAL NEOPLASMS; GENETIC COUNSELING; GENETIC PREDISPOSITION TO DISEASE; HUMANS; IMMUNOHISTOCHEMISTRY; INTESTINAL POLYPOSIS; INTESTINAL POLYPS; MALE; MONITORING, PHYSIOLOGIC; PEDIATRICS; PEDIGREE; PROGNOSIS; RISK ASSESSMENT;

EID: 33646849300     PISSN: 1042895X     EISSN: 15389766     Source Type: Journal    
DOI: 10.1097/00001610-200601000-00003     Document Type: Article

References (32)

1. Attard, T.M. (2003). Diagnosis and management issues in pediatric patients with gastrointestinal polyps. Practical Gastroenterology, April, 57-72.
2. Attard, T.M., Cuffari, C., Tajouri, T., Stoner, J.A., Eisenberg, M.T., Yardley, J.H., et al. (2004). Multicenter experience with upper gastrointestinal polyps in pediatric patients with familial adenomatous polyposis. American Journal of Gastroenterology, 99(4), 681-686.
3. Attard, T.M., Howe, F.C., & Lynch, H.T. (2004). The hereditary mixed polyposis syndrome may be associated with mutation in the BMPR1A gene on chromosome 10q22.3. Journal of Pediatric Gastroenterology and Nutrition, 39(Suppl. 1), S452.
4. Barrison, A.F., Smith, C., Oviedo, J., Heeren, T., & Schroy, P.C. (2003). Colorectal cancer screening and familial risk: A survey of internal medicine residents' knowledge and practice patterns. American Journal of Gastroenterology, 98(6), 1410-1416.
5. Bertario, L., Russo, A., Radice, P., Varesco, L., Eboli, M., Spinelli, P., et al. (2000). Genotype and phenotype factors as determinants for rectal stump cancer in patients with familial adenomatous polyposis. Hereditary Colorectal Tumors Registry. Annals of Surgery, 231(4), 538-543.
6. Bulow, C., Vasen, H., Jarvinen, H., Bjork, J., Bisgaard, M.L., & Bulow, S. (2000). Ileorectal anastomosis is appropriate for a subset of patients with familial adenomatous polyposis. Gastroenterology, 119(6), 1454-1460.
7. Codori, A.M., Zawacki, K.L., Petersen, G.M., Miglioretti, D.L., Bacon, J.A., et al. (2003). Genetic testing for hereditary colorectal cancer in children: Long-term psychological effects. American Journal of Medical Genetics, 116(2), 117-128.
8. Cronkhite, L.W., & Canada, W.J. (1955). Generalized gastrointestinal polyposis: An unusual syndrome of polyposis, pigmentation, alopecia and onychotrophia. New England Journal of Medicine, 252, 1011-1015.
9. Eng, C. (2003). PTEN: One gene, many syndromes. Human Mutation, 22(3), 183-198.
10. Entius, M.M., Westerman, A.M., vanVelthusen, M.L., Wilson, J.H., Hamilton, S.R., Giardiello, F.M., et al. (1999). Molecular and phenotypic markers of hamartomatous polyposis syndromes in the gastrointestinal tract. Hepatogastroenterology, 46(26), 661-666.
11. Giardiello, F.M., Petersen, G.M., Piantadosi, S., Gruber, S.B., Traboulsi, E., Offerhause, G.J., et al. (1997). APC gene mutations and extraintestinal phenotype of familial adenomatous polyposis. Gut, 40(4), 521-525.
12. Gornick, M.E., Eggers, P.W., & Riley, G.F. (2004). Associations of race, education, and patterns of preventive service use with stage of cancer at time of diagnosis. Health Services Research, 39(5), 1403-1427.
13. Grobmyer, S.R., Guillem, J.G., O'Riordain, D.S., Woodruff, J.M., Shriver, C., & Brennan, M.F. (1999). Colonic manifestations of multiple endocrine neoplasia type 2B: Report of four cases. Diseases of the Colon & Rectum, 42(9), 1216-1219.
14. Gupta, S.K., Fitzgerald, J. F, Croffie, J.M., Chong, S.K., Pfefferkorn, M.C., Davis, M.M., et al. (2001). Experience with juvenile polyps in North American children: The need for pancolonoscopy. American Journal of Gastroenterology, 96(6), 1695-1697.
15. Howe, J.R., Bair, J.L., Sayed, M.G., Anderson, M.E., Mitros, F.A., Petersen, G.M., et al. (2001). Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis. Nature Genetics, 28(2), 184-187.
16. Jaeger, E.E., Woodford-Richens, K.L., Lockett, M., Rowan, A.J., Sawyer, E.J., Heinimann, K., et al. (2003). An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome. American Journal of Human Genetics, 72(5), 1261-1267.
17. Jass, J.R., Williams, C.B., Bussey, H.J., & Morson, B.C. (1998). Juvenile polyposis—a precancerous condition. Histopathology, 13(6), 619-630.
18. Kinzler, K.W., Nilbert, M.C., Vogelstein, B., Bryan, T.M., Levy, D. B, Smith, K.J., et al. (1991). Identification of a gene located at chromosome 5q21 that is mutated in colorectal cancers. Science, 251(4999), 1366-1370.
19. Lim, W., Olschwang, S., Keller, J.J., Westerman, A.M., Menko, F.H., Boardman, L.A., et al. (2004). Relative frequency and morphology of cancers in STK11 mutation carriers. Gastroenterology, 126(7), 1788-1794.
20. Marsh, D.J., Kum, J.B., Lunetta, K.L., Bennett, M.J., Gorlin, R.J., Ahmend, S.F., et al. (1999). Germline PTEN mutations in Cowden syndrome-like families. Human Molecular Genetics, 8(8), 1461-1472.
21. Merg, A., & Howe, J.R. (2004). Genetic conditions associated with intestinal juvenile polyps. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 129(1), 44-55.
22. Michie, S., Bobrow, M., Marteau, T.M., Saidi, G., Goodburn, S., Lawton, J., et al. (2001). Predictive genetic testing in children and adults: A study of emotional impact? Journal of Medical Genetics, 38(8), 519-526.
23. Murday, V., & Slack, J. (1989). Inherited disorders associated with colorectal cancer. Cancer Survivor, 8(1), 139-157.
24. Nugent, K.P., Talbot, I.C., Hodgson, S.V., & Phillips, R.K. (1993). Solitary juvenile polyps: Not a marker for subsequent malignancy. Gastroenterology, 105(3), 698-700.
25. Oncel, M., Church, J.M., Remizi, F.H., & Fazio, V.W. (2005). Colonic surgery in patients with juvenile polyposis syndrome: A case series. Diseases of the Colon & Rectum, 48(1), 49-56.
26. Parc, Y.R., Olschwang, S., Desaint, B., Schmitt, G., Parc, R.G., & Tiret, E. (2001). Familial adenomatous polyposis: Prevalence of adenomas in the ileal pouch after restorative proctocolectomy. Annals of Surgery, 233(3), 360-364.
27. Pilarski, R., & Eng, C. (2004). Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome. Journal of Medical Genetics, 41(5), 323-326.
28. Sampson, J.R., Dolwani, S., Jones, S., Eccles, D., Ellis, A., Evans, D.G., et al. (2003). Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH. Lancet, 362(9377), 39-41.
29. Schreibman, I.R., Baker, M., Amos, C., & McGarrity, T.J. (2005). The hamartomatous polyposis syndromes: A clinical and molecular review. American Journal of Gastroenterology, 100(2), 476-490.
30. Wu, T.T., Rezai, B., Rashid, A., Luce, M.C., Cayouette, M.C., Kim, C., et al. (1997). Genetic alterations and epithelial dysplasia in juvenile polyposis syndrome and sporadic juvenile polyps. American Journal of Pathology, 150(3), 939-947.
31. Wyllie, R.A.H., & Jeffrey S. (Eds.). (1999). Pediatric gastrointestinal disease (2nd ed.; pp. 315-333). Philadelphia: W.B. Saunders.
32. Ziv, Y., Church, J.M., Oakely, J.R., McGannon, E., Schroeder, T.K., & Fazio, V.F. (1996). Results after restorative proctocolectomy and ileal pouch-anal anastomosis in patients with familial adenomatous polyposis and coexisting colorectal cancer. British Journal of Surgery, 83(11), 1578-1580.