Clinical and Biologic Features of Adenomatosis Coli in Northern Italy

References

• Haggitt R C, Brian J, Reid MD. Hereditary gastrointestinal polyposis syndromes. Am J Surg Pathol 1986; 10: 871–87
   PubMed Web of Science ®Google Scholar
• Bulow S. Special selection: premalignant conditions of the gastrointestinal tract. Ann Med 1989; 21: 299–307
   PubMed Web of Science ®Google Scholar
• Alm T. Hereditary adenomatosis of the colon and rectum. Colon cancer genetics, P M Lynch, H T Lynch. Von Nostrand Reinhold Company, New York 1985
   Google Scholar
• Gardner EJ. Genetic and clinical study of intestinal polyposis, predisposing factor to carcinoma of the colon and rectum. Am J Hum Genet 1951; 3: 167–76
   PubMed Web of Science ®Google Scholar
• Turcot J, Despes J P, St Pierre F. Malignant tumours of the central nervous system associated with familial polyposis of the colon. Report of two cases. Dis Col Rectum 1959; 2: 465–8
   PubMedGoogle Scholar
• Evans D GR, Guy S P, Thakker N, Armstrong J G, Dodd C, Davies D R, et al. Non-penetrance and late appearance of polyps in families with familial adenomatous polyposis. Gut 1993; 34: 1389–93
   PubMedGoogle Scholar
• Herrera L, Kakati S, Gibas L, Pietrzak E, Sandberg AA. Brief clinical report: Gardner syndrome in a man with an interstitial deletion of 5q. Am J Med Genet 1986; 25: 473–6
   PubMed Web of Science ®Google Scholar
• Bodmer W F, Bailey C J, Bodmer J, Bussey H JR, Ellis A, Gorman P, et al. Localization of the gene for familial adenomatosis polyposis of chromosome 5. Nature 1987; 328: 614–6
   PubMed Web of Science ®Google Scholar
• Leppert M, Dobbs M, Scambler P, O'Connell P, Nakamura Y, Stauffer D, et al. The gene for familial polyposis coli maps to the long arm of chromosome 5. Science 1987; 238: 1411–3
   PubMed Web of Science ®Google Scholar
• Kinzler K, Nilbert M, Su L K, Vogelstein B, Bryan T M, Levy D B, et al. Identification of FAP locus gene from chromosome 5q21. Science 1991; 253: 661–9
   PubMed Web of Science ®Google Scholar
• Varesco L, Gismondi V, James R, Robertson M, Grammatico P, Groden J, et al. Identification of APC gene mutations in Italian adenomatous polyposis coli, patients by PCR-SSCP analysis. Am J Hum Genet 1993; 52: 280–5
   PubMedGoogle Scholar
• Pow de Leon M, Sassatelli R, Scalmati A, Di Gregorio C, Fante R, Zanghieri G, et al. Descriptive epidemiology of colorectal cancer in Italy. Eur J Cancer 1993; 29A: 367–71
   PubMedGoogle Scholar
• Ponz de Leon M, Sassatelli R, Zanghieri G, Sacchetti C, Roncucci L, Scalmati A, et al. Hereditary adenomatosis of the colon and rectum: clinical features of eight families from Northern Italy. Am J Gastroenterol 1989; 84: 906–16
   PubMedGoogle Scholar
• Traboulsi A I, Krush A J, Gardner E J, Booker S V, Offerhaus G JA, Yardley J H, et al. Prevalence and importance of pigmented ocular fundus lesions in Gardner's syndrome. N Engl J Med 1987; 316: 661–7
   PubMed Web of Science ®Google Scholar
• Heyen F, Jagelman D G, Romania A, Zakov Z N, Lavery I C, Fazio V W, et al. Predictive value of congenital hypertrophy of the retinal pigment epithelium as a clinical marker for familial adenomatous polyposis. Dis Col Rectum 1990; 33: 1003–8
   PubMed Web of Science ®Google Scholar
• Woods R J, Sarre R G, Ctercteko G C, Jagelman D J, Smith J W, Duchesneau P M, et al. Occult radiologic changes in the skull and jaw in familial adenomatous polyposis coli. Dis Colon Rectum 1989; 32: 304–6
   PubMedGoogle Scholar
• Johan G, Offerhaus A, Levin L S, Giardiello F M, Krush A J, Welsh S B, et al. Occult radiopaque jaw lesions in familial adenomatous polyposis coli and hereditary nonpolyposis colorectal cancer. Gastroenterology 1987; 93: 490–7
   PubMedGoogle Scholar
• Alm T, Licznerski G. The intestinal polyposis. Clin Gastroenterol 1973; 2: 577–602
   Google Scholar
• Morton N E, Rao D C, Lalouel JM. Methods in genetic epidemiology. Karger, Basel 1983; 62–9
   Google Scholar
• Ponz de Leon M, Scapoli C, Zanghieri G, Sassatelli R, Saccetti C, Barrai I. Genetic transmission of colorectal cancer: exploratory data analysis from a population based registry. J Med Genet 1992; 29: 531–8
   PubMedGoogle Scholar
• Mecklin J P, Jawinen H J, Peltokallio P. Cancer family syndrome. Genetic analysis of 22 Finnish kindreds. Gastroenterology 1986; 90: 32633
   Google Scholar
• Zeuthen J. Epstein-Barr virus (EBV), lymphocytes and transformation. J Cancer Res Clin Oncol 1983; 1M: 1–11
   Google Scholar
• Sarnbrook J, Fritsch E F, Maniatis T. Molecular cloning: a laboratory manual2nd ed. Cold Spring Harbor Laboratory, Cold Spring Harbor (NY) 1989
   Google Scholar
• Utsunomiya J, Iwama T. Adenomatosis coli in Japan. Colorectal cancer prevention, epidemiology and screening, S Winawer, D Schottenfeld, P Sherlock. Raven Press, New York 1980; 83–95
   Google Scholar
• Utsunomiya J, Murata M, Tanimura M. An analysis of the age distribution of colon cancer in adenomatosis coli. Cancer 1980; 45: 198–205
   PubMed Web of Science ®Google Scholar
• Järvinen HJ. Epidemiology of familial adenomatous polyposis in Finland: impact of family screening on the colorectal cancer rate and survival. Gut 1992; 33: 357–60
   PubMed Web of Science ®Google Scholar
• Bussey H JR. Familial polyposis coli. Family studies, histopathology, differential diagnosis and results of treatment. The Johns Hopkins University Press, Baltimore 1975
   Google Scholar
• Berk T, Biilow S, Cohen Z, De Cosse J J, Hawley P R, Jagelman D G, et al. Surgical aspects of familial adenomatous polyposis. Int J Colorectal Dis 1988; 3: 1–16
   PubMed Web of Science ®Google Scholar
• Iwama T, Mishima Y, Utsunomiya J. The impact of familial adenomatous polyposis on the tumorigenesis and mortality at the several organs. Ann Surg 1993; 217: 101–8
   PubMed Web of Science ®Google Scholar
• Naylor E W, Lebenthal E. Gardner's syndrome. Recent developments in research and management. Dig Dis Sci 1980; 25: 945–59
   PubMedGoogle Scholar
• Veale A MO. Intestinal polyposis. Eugenics laboratory memoirs (Galton Laboratory). Cambridge University Press, Cambridge 1965; 40
   Google Scholar
• Naylor E W, Gardner EJ. Penetrance and expressivity of the gene responsible for the Gardner's syndrome. Clin Genet 1977; 11: 381–93
   PubMedGoogle Scholar
• Spigelman A D, Williams C B, Talbot I C, Domizio P, Phillips R KS. Upper gastrointestinal cancer in patients with familial adenomatous polyposis. Lancet 1989; 2: 783–5
   PubMed Web of Science ®Google Scholar
• Iida M, Yao T, Itoh H, Watanabe H, Matsui T, Iwashita A, et al. Natural history of gastric adenomas in patients with familial adenomatosis coli/Gardner's syndrome. Cancer 1988; 61: 605–11
   PubMedGoogle Scholar
• Iida M, Yao T, Itoh H, et al. Natural history of duodenal lesions in Japanese patients with familial adenomatosis coli (Gardner's syndrome). Gastroenterology 1989; 96: 1301–6
   PubMed Web of Science ®Google Scholar
• Sarre R G, Frost A G, Jagelman D G, Petras R E, Sivak M V, McGannon E. Gastric and duodenal polyps in familial adenomatous polyposis: a prospective study of the nature and prevalence of upper gastrointestinal polyps. Gut 1987; 28: 306–14
   PubMed Web of Science ®Google Scholar
• Myrhøj T, Bulow S, Mogensen AM. Multiple adenomas in terminal ileum 25 years after restorative proctolectomy for familial adenomatous polyposis. Dis Colon Rectum 1989; 32: 618–20
   PubMedGoogle Scholar
• Gilson T P, Sollenberg LL. Adenocarcinoma of an ileostomy in a patient with familial adenomatous polyposis. Dis Colon Rectum 1992; 35: 261–5
   PubMedGoogle Scholar
• Iida M, Itoh H, Matsui T, Mibu R, Iwashita A, Fujishima M. Ileal adenomas in postcolectomy patients with familial adenomatosis coli/Gardner's syndrome. Dis Colon Rectum 1989; 32: 1034–8
   PubMedGoogle Scholar
• Purcell J J, Shields JA. Hypertrophy with hyperpigmentation of the retinal pigment epithelium. Arch Ophthalmol 1975; 93: 1122–6
   PubMedGoogle Scholar
• Baker R H, Heinemann M H, Miller H H, De Cosse J. Hyper-pigmented lesions of the retinal pigment epithelium in familial adenomatous polyposis. Am J Med Genet 1988; 31: 427–35
   PubMedGoogle Scholar
• Baba S, Tsuchiya M, Watanabe I, Machida H. Importance of retinal pigmentation as a subclinical marker in familial adenomatous polyposis. Dis Colon Rectum 1990; 33: 66–5
   Google Scholar
• Norris J L, Leasby GS. An unusual case of congenital hypertrophy of the retinal pigment epithelium. Arch Ophthalmol 1976; 94: 1910–1
   PubMedGoogle Scholar
• Utsunomiya J, Nakamura T. The occult osteomatous changes in the mandible in patients with familial polyposis coli. Br J Surg 1975; 62: 45–51
   PubMed Web of Science ®Google Scholar
• Giardiello F M, Offerhaus G JA, Traboulsi E I, Graybeal J C, Maumenee I H, Krush A J, et al. Value of combined phenotypic markers in identifying inheritance of familial adenomatous polyposis. Gut 1991; 32: 1170–4
   PubMed Web of Science ®Google Scholar
• Olschwang S, Puig P L, Groden J, White R, Thomas G. Germ-line mutations in the first 14 exons of the adenomatous polyposis coli (APC) gene. Am J Hum Genet 1993; 52: 273–9
   PubMedGoogle Scholar
• Groden J, Gelbert L, Thliveris A, Nelson L, Robertson M, Joslyn G, et al. Mutational analysis of patients with adenomatous polyposis: identical inactivating mutations in unrelated individuals. Am J Hum Genet 1993; 52: 263–72
   PubMedGoogle Scholar
• Leppert H. Atypical FAP and hereditary non-polyposis colorectal cancer. Proceedings of the 27th Annual Clinical Conference on Advances in the Biology and Therapy of Colorectal Cancer. 1993. Houston Nov 4–7, 1993
   Google Scholar