메뉴 건너뛰기




Volumn 21, Issue 3, 2007, Pages 409-426

The patient with multiple intestinal polyps

Author keywords

cancer risk; FAP; hereditary colorectal cancer syndromes; juvenile polyposis; Peutz Jeghers syndrome; polyposis syndromes

Indexed keywords

APC PROTEIN; CELECOXIB; DNA GLYCOSYLASE MUTY; ENEMA; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE; SULINDAC;

EID: 34249731563     PISSN: 15216918     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bpg.2006.11.003     Document Type: Article
Times cited : (24)

References (81)
  • 1
    • 0025817880 scopus 로고
    • Identification of FAP locus genes from chromosome 5q21
    • Kinzler K.W., Nilbert M.C., Su L.K., et al. Identification of FAP locus genes from chromosome 5q21. Science 253 (1991) 661-665
    • (1991) Science , vol.253 , pp. 661-665
    • Kinzler, K.W.1    Nilbert, M.C.2    Su, L.K.3
  • 2
    • 1442290391 scopus 로고    scopus 로고
    • Surveillance of duodenal adenomas in familial adenomatous polyposis reveals high cumulative risk of advanced disease
    • Saurin J.C., Gutknecht C., Napoleon B., et al. Surveillance of duodenal adenomas in familial adenomatous polyposis reveals high cumulative risk of advanced disease. J Clin Oncol 22 (2004) 493-498
    • (2004) J Clin Oncol , vol.22 , pp. 493-498
    • Saurin, J.C.1    Gutknecht, C.2    Napoleon, B.3
  • 3
    • 10744228081 scopus 로고    scopus 로고
    • Duodenal adenomatosis in familial adenomatous polyposis
    • Bulow S., Bjork J., Christensen I.J., et al. Duodenal adenomatosis in familial adenomatous polyposis. Gut 53 (2004) 381-386
    • (2004) Gut , vol.53 , pp. 381-386
    • Bulow, S.1    Bjork, J.2    Christensen, I.J.3
  • 4
    • 0036102596 scopus 로고    scopus 로고
    • Duodenal cancer in patients with familial adenomatous polyposis (FAP): results of a 10 year prospective study
    • Groves C.J., Saunders B.P., Spigelman A.D., and Phillips R.K. Duodenal cancer in patients with familial adenomatous polyposis (FAP): results of a 10 year prospective study. Gut 50 (2002) 636-641
    • (2002) Gut , vol.50 , pp. 636-641
    • Groves, C.J.1    Saunders, B.P.2    Spigelman, A.D.3    Phillips, R.K.4
  • 5
    • 0032876169 scopus 로고    scopus 로고
    • Management of duodenal adenomas in 98 patients with familial adenomatous polyposis
    • Heiskanen I., Kellokumpu I., and Jarvinen H. Management of duodenal adenomas in 98 patients with familial adenomatous polyposis. Endoscopy 31 (1999) 412-416
    • (1999) Endoscopy , vol.31 , pp. 412-416
    • Heiskanen, I.1    Kellokumpu, I.2    Jarvinen, H.3
  • 6
    • 0035052054 scopus 로고    scopus 로고
    • Duodenal adenomatosis in familial adenomatous polyposis coli. A review of the literature and results from the Heidelberg Polyposis Register
    • Kadmon M., Tandara A., and Herfarth C. Duodenal adenomatosis in familial adenomatous polyposis coli. A review of the literature and results from the Heidelberg Polyposis Register. Int J Colorectal Dis 16 (2001) 63-75
    • (2001) Int J Colorectal Dis , vol.16 , pp. 63-75
    • Kadmon, M.1    Tandara, A.2    Herfarth, C.3
  • 7
    • 0026537747 scopus 로고
    • The risk of upper gastrointestinal cancer in familial adenomatous polyposis
    • Offerhaus G.J., Giardiello F.M., Krush A.J., et al. The risk of upper gastrointestinal cancer in familial adenomatous polyposis. Gastroenterology 102 (1992) 1980-1982
    • (1992) Gastroenterology , vol.102 , pp. 1980-1982
    • Offerhaus, G.J.1    Giardiello, F.M.2    Krush, A.J.3
  • 8
    • 0032884657 scopus 로고    scopus 로고
    • Causes of death in familial adenomatous polyposis
    • Galle T.S., Juel K., and Bulow S. Causes of death in familial adenomatous polyposis. Scand J Gastroenterol 34 (1999) 808-812
    • (1999) Scand J Gastroenterol , vol.34 , pp. 808-812
    • Galle, T.S.1    Juel, K.2    Bulow, S.3
  • 9
    • 0024342360 scopus 로고
    • Upper gastrointestinal cancer in patients with familial adenomatous polyposis
    • Spigelman A.D., Williams C.B., Talbot I.C., et al. Upper gastrointestinal cancer in patients with familial adenomatous polyposis. Lancet (1989) 783-785
    • (1989) Lancet , pp. 783-785
    • Spigelman, A.D.1    Williams, C.B.2    Talbot, I.C.3
  • 10
    • 13744254325 scopus 로고    scopus 로고
    • Feasibility and diagnostic utility of video capsule endoscopy for the detection of small bowel polyps in patients with hereditary polyposis syndromes
    • Schulmann K., Hollerbach S., Kraus K., et al. Feasibility and diagnostic utility of video capsule endoscopy for the detection of small bowel polyps in patients with hereditary polyposis syndromes. Am J Gastroenterol 100 (2005) 27-37
    • (2005) Am J Gastroenterol , vol.100 , pp. 27-37
    • Schulmann, K.1    Hollerbach, S.2    Kraus, K.3
  • 11
    • 22744458880 scopus 로고    scopus 로고
    • The utility of capsule endoscopy small bowel surveillance in patients with polyposis
    • Burke C.A., Santisi J., Church J., and Levinthal G. The utility of capsule endoscopy small bowel surveillance in patients with polyposis. Am J Gastroenterol 100 (2005) 1498-1502
    • (2005) Am J Gastroenterol , vol.100 , pp. 1498-1502
    • Burke, C.A.1    Santisi, J.2    Church, J.3    Levinthal, G.4
  • 12
    • 1242296357 scopus 로고    scopus 로고
    • Long-term outcome of familial adenomatous polyposis patients after restorative coloproctectomy
    • Parc Y., Piquard A., Dozois R.R., et al. Long-term outcome of familial adenomatous polyposis patients after restorative coloproctectomy. Ann Surg 239 (2004) 378-382
    • (2004) Ann Surg , vol.239 , pp. 378-382
    • Parc, Y.1    Piquard, A.2    Dozois, R.R.3
  • 13
    • 0035076731 scopus 로고    scopus 로고
    • Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families
    • Friedl W., Caspari R., Sengteller, et al. Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families. Gut 48 (2001) 515-521
    • (2001) Gut , vol.48 , pp. 515-521
    • Friedl, W.1    Caspari, R.2    Sengteller3
  • 14
    • 0027769633 scopus 로고
    • Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients
    • Olschwang S., Tiret A., Laurent-Puig P., et al. Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients. Cell 75 (1993) 959-968
    • (1993) Cell , vol.75 , pp. 959-968
    • Olschwang, S.1    Tiret, A.2    Laurent-Puig, P.3
  • 15
    • 19244364521 scopus 로고    scopus 로고
    • Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene
    • Eccles D.M., van der Luijt R., Breukel C., et al. Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene. Am J Hum Genet 59 (1996) 1193-1201
    • (1996) Am J Hum Genet , vol.59 , pp. 1193-1201
    • Eccles, D.M.1    van der Luijt, R.2    Breukel, C.3
  • 16
    • 0034126868 scopus 로고    scopus 로고
    • Genotype and phenotype factors as determinants for rectal stump cancer in patients with familial adenomatous polyposis. Hereditary Colorectal Tumors Registry
    • Bertario L., Russo A., Radice P., et al. Genotype and phenotype factors as determinants for rectal stump cancer in patients with familial adenomatous polyposis. Hereditary Colorectal Tumors Registry. Ann Surg 231 (2000) 538-543
    • (2000) Ann Surg , vol.231 , pp. 538-543
    • Bertario, L.1    Russo, A.2    Radice, P.3
  • 17
    • 0034465534 scopus 로고    scopus 로고
    • Ileorectal anastomosis is appropriate for a subset of patients with familial adenomatous polyposis
    • Bulow C., Vasen H., Järvinen H., et al. Ileorectal anastomosis is appropriate for a subset of patients with familial adenomatous polyposis. Gastroenterology 119 (2000) 1454-1460
    • (2000) Gastroenterology , vol.119 , pp. 1454-1460
    • Bulow, C.1    Vasen, H.2    Järvinen, H.3
  • 18
    • 0031917031 scopus 로고    scopus 로고
    • APC genotype, polyp number, and surgical options in familial adenomatous polyposis
    • Wu J.S., Paul P., McGannon E.A., and Church J.M. APC genotype, polyp number, and surgical options in familial adenomatous polyposis. Ann Surg 227 (1998) 57-62
    • (1998) Ann Surg , vol.227 , pp. 57-62
    • Wu, J.S.1    Paul, P.2    McGannon, E.A.3    Church, J.M.4
  • 19
    • 0000778913 scopus 로고    scopus 로고
    • Group aTCLP Guidelines for the surveillance and managemnet of familial adenomatous polyposis (FAP): a world wide survey among 41 registries
    • Vasen H.F., and Bulow S. Group aTCLP Guidelines for the surveillance and managemnet of familial adenomatous polyposis (FAP): a world wide survey among 41 registries. Colorectal Dis 1 (2001) 214-221
    • (2001) Colorectal Dis , vol.1 , pp. 214-221
    • Vasen, H.F.1    Bulow, S.2
  • 20
    • 0037310758 scopus 로고    scopus 로고
    • Colorectal cancer screening and surveillance: clinical guidelines and rationale - update based on new evidence
    • Winawer S., Fletcher R., Rex D., et al. Colorectal cancer screening and surveillance: clinical guidelines and rationale - update based on new evidence. Gastroenterology 124 (2003) 544-560
    • (2003) Gastroenterology , vol.124 , pp. 544-560
    • Winawer, S.1    Fletcher, R.2    Rex, D.3
  • 22
    • 27644521343 scopus 로고    scopus 로고
    • Pancreas-sparing duodenectomy is effective management for familial adenomatous polyposis
    • Mackey R., Walsh R.M., Chung R., et al. Pancreas-sparing duodenectomy is effective management for familial adenomatous polyposis. J Gastrointest Surg 9 (2005) 1088-1093
    • (2005) J Gastrointest Surg , vol.9 , pp. 1088-1093
    • Mackey, R.1    Walsh, R.M.2    Chung, R.3
  • 23
    • 17744418769 scopus 로고    scopus 로고
    • The effect of celecoxib, a cyclooxygenase-2 inhibitor, in familial adenomatous polyposis
    • Steinbach G., Lynch P.M., Phillips R.K., et al. The effect of celecoxib, a cyclooxygenase-2 inhibitor, in familial adenomatous polyposis. N Engl J Med 342 (2000) 1946-1952
    • (2000) N Engl J Med , vol.342 , pp. 1946-1952
    • Steinbach, G.1    Lynch, P.M.2    Phillips, R.K.3
  • 24
    • 0036114348 scopus 로고    scopus 로고
    • A randomised, double blind, placebo controlled study of celecoxib, a selective cyclooxygenase 2 inhibitor, on duodenal polyposis in familial adenomatous polyposis
    • Phillips R.K., Wallace M.H., Lynch P.M., et al. A randomised, double blind, placebo controlled study of celecoxib, a selective cyclooxygenase 2 inhibitor, on duodenal polyposis in familial adenomatous polyposis. Gut 50 (2002) 857-860
    • (2002) Gut , vol.50 , pp. 857-860
    • Phillips, R.K.1    Wallace, M.H.2    Lynch, P.M.3
  • 25
    • 0037961628 scopus 로고    scopus 로고
    • Attenuated familial adenomatous polyposis (AFAP). A review of the literature
    • Knudsen A.L., Bisgaard M.L., and Bulow S. Attenuated familial adenomatous polyposis (AFAP). A review of the literature. Fam Cancer 2 (2003) 43-55
    • (2003) Fam Cancer , vol.2 , pp. 43-55
    • Knudsen, A.L.1    Bisgaard, M.L.2    Bulow, S.3
  • 26
    • 4143082647 scopus 로고    scopus 로고
    • Genetic testing and phenotype in a large kindred with attenuated familial adenomatous polyposis
    • Burt R.W., Leppert M.F., Slattery M.L., et al. Genetic testing and phenotype in a large kindred with attenuated familial adenomatous polyposis. Gastroenterology 127 (2004) 444-451
    • (2004) Gastroenterology , vol.127 , pp. 444-451
    • Burt, R.W.1    Leppert, M.F.2    Slattery, M.L.3
  • 27
    • 0027724691 scopus 로고
    • Alleles of the APC gene: an attenuated form of familial polyposis
    • Spirio L., Olschwang S., Groden J., et al. Alleles of the APC gene: an attenuated form of familial polyposis. Cell 75 (1993) 951-957
    • (1993) Cell , vol.75 , pp. 951-957
    • Spirio, L.1    Olschwang, S.2    Groden, J.3
  • 28
    • 0031691330 scopus 로고    scopus 로고
    • Variable phenotype of familial adenomatous polyposis in pedigrees with 3′ mutation in the APC gene
    • Brensinger J.D., Laken S.J., Luce M.C., et al. Variable phenotype of familial adenomatous polyposis in pedigrees with 3′ mutation in the APC gene. Gut 43 (1998) 548-552
    • (1998) Gut , vol.43 , pp. 548-552
    • Brensinger, J.D.1    Laken, S.J.2    Luce, M.C.3
  • 29
    • 33745903402 scopus 로고    scopus 로고
    • MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype
    • Aretz S., Uhlhaas S., Goergens H., et al. MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype. Int J Cancer 119 (2006) 807-814
    • (2006) Int J Cancer , vol.119 , pp. 807-814
    • Aretz, S.1    Uhlhaas, S.2    Goergens, H.3
  • 30
    • 26244444771 scopus 로고    scopus 로고
    • Correlation of polyp number and family history of colon cancer with germline MYH mutations
    • Jo W.S., Bandipalliam P., Shannon K.M., et al. Correlation of polyp number and family history of colon cancer with germline MYH mutations. Clin Gastroenterol Hepatol 3 (2005) 1022-1028
    • (2005) Clin Gastroenterol Hepatol , vol.3 , pp. 1022-1028
    • Jo, W.S.1    Bandipalliam, P.2    Shannon, K.M.3
  • 31
    • 0037468517 scopus 로고    scopus 로고
    • Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH
    • Sieber O.M., Lipton L., Crabtree M., et al. Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH. N Engl J Med 348 (2003) 791-799
    • (2003) N Engl J Med , vol.348 , pp. 791-799
    • Sieber, O.M.1    Lipton, L.2    Crabtree, M.3
  • 32
    • 3242689475 scopus 로고    scopus 로고
    • MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps
    • Wang L., Baudhuin L.M., Boardman L.A., et al. MYH mutations in patients with attenuated and classic polyposis and with young-onset colorectal cancer without polyps. Gastroenterology 127 (2004) 9-16
    • (2004) Gastroenterology , vol.127 , pp. 9-16
    • Wang, L.1    Baudhuin, L.M.2    Boardman, L.A.3
  • 33
    • 2942538325 scopus 로고    scopus 로고
    • High frequency of MYH gene mutations in a subset of patients with familial adenomatous polyposis
    • Venesio T., Molatore S., Cattaneo F., et al. High frequency of MYH gene mutations in a subset of patients with familial adenomatous polyposis. Gastroenterology 126 (2004) 1681-1685
    • (2004) Gastroenterology , vol.126 , pp. 1681-1685
    • Venesio, T.1    Molatore, S.2    Cattaneo, F.3
  • 34
    • 3543020359 scopus 로고    scopus 로고
    • The multiple colorectal adenoma phenotype and MYH, a base excision repair gene
    • Lipton L., and Tomlinson I. The multiple colorectal adenoma phenotype and MYH, a base excision repair gene. Clin Gastroenterol Hepatol 2 (2004) 633-638
    • (2004) Clin Gastroenterol Hepatol , vol.2 , pp. 633-638
    • Lipton, L.1    Tomlinson, I.2
  • 35
    • 33645836699 scopus 로고    scopus 로고
    • Novel findings in Swedish patients with MYH-associated polyposis: mutation detection and clinical characterization
    • Kanter-Smoler G., Bjork J., Fritzell K., et al. Novel findings in Swedish patients with MYH-associated polyposis: mutation detection and clinical characterization. Clin Gastroenterol Hepatol 4 (2006) 499-506
    • (2006) Clin Gastroenterol Hepatol , vol.4 , pp. 499-506
    • Kanter-Smoler, G.1    Bjork, J.2    Fritzell, K.3
  • 36
    • 33746775351 scopus 로고    scopus 로고
    • Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)
    • Nielsen M., Franken P.F., Reinards T.H., et al. Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP). J Med Genet 42 (2005) e54
    • (2005) J Med Genet , vol.42
    • Nielsen, M.1    Franken, P.F.2    Reinards, T.H.3
  • 38
    • 0032893658 scopus 로고    scopus 로고
    • Allelic imbalance at the LKB1 (STK11) locus in tumours from patients with Peutz-Jeghers' syndrome provides evidence for a hamartoma-adenoma-carcinoma sequence
    • Wang Z.J., Ellis I., Zauber P., et al. Allelic imbalance at the LKB1 (STK11) locus in tumours from patients with Peutz-Jeghers' syndrome provides evidence for a hamartoma-adenoma-carcinoma sequence. J Pathol 188 (1999) 9-13
    • (1999) J Pathol , vol.188 , pp. 9-13
    • Wang, Z.J.1    Ellis, I.2    Zauber, P.3
  • 39
    • 0034464147 scopus 로고    scopus 로고
    • Very high risk of cancer in familial Peutz-Jeghers syndrome
    • Giardiello F.M., Brensinger J.D., Tersmette A.C., et al. Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology 119 (2000) 1447-1453
    • (2000) Gastroenterology , vol.119 , pp. 1447-1453
    • Giardiello, F.M.1    Brensinger, J.D.2    Tersmette, A.C.3
  • 40
    • 33744782567 scopus 로고    scopus 로고
    • Frequency and spectrum of cancers in the Peutz-Jeghers syndrome
    • Hearle N., Schumacher V., Menko F.H., et al. Frequency and spectrum of cancers in the Peutz-Jeghers syndrome. Clin Cancer Res 12 (2006) 3209-3215
    • (2006) Clin Cancer Res , vol.12 , pp. 3209-3215
    • Hearle, N.1    Schumacher, V.2    Menko, F.H.3
  • 41
    • 33745480336 scopus 로고    scopus 로고
    • Cancer risks in LKB1 germline mutation carriers
    • Mehenni H., Resta N., Park J.G., et al. Cancer risks in LKB1 germline mutation carriers. Gut 55 (2006) 984-990
    • (2006) Gut , vol.55 , pp. 984-990
    • Mehenni, H.1    Resta, N.2    Park, J.G.3
  • 42
    • 15444350943 scopus 로고    scopus 로고
    • Increased risk for cancer in patients with the Peutz-Jeghers syndrome
    • Boardman L.A., Thibodeau S.N., Schaid, et al. Increased risk for cancer in patients with the Peutz-Jeghers syndrome. Ann Intern Med 128 (1998) 896-899
    • (1998) Ann Intern Med , vol.128 , pp. 896-899
    • Boardman, L.A.1    Thibodeau, S.N.2    Schaid3
  • 43
    • 0014784453 scopus 로고
    • Sex cord tumor with annular tubules a distinctive ovarian tumor of the Peutz-Jeghers syndrome
    • Scully R.E. Sex cord tumor with annular tubules a distinctive ovarian tumor of the Peutz-Jeghers syndrome. Cancer 25 (1970) 1107-1121
    • (1970) Cancer , vol.25 , pp. 1107-1121
    • Scully, R.E.1
  • 44
    • 0025970813 scopus 로고
    • An aromatase-producing sex-cord tumor resulting in prepubertal gynecomastia
    • Coen P., Kulin H., Ballantine T., et al. An aromatase-producing sex-cord tumor resulting in prepubertal gynecomastia. N Engl J Med 324 (1991) 317-322
    • (1991) N Engl J Med , vol.324 , pp. 317-322
    • Coen, P.1    Kulin, H.2    Ballantine, T.3
  • 45
    • 0032495530 scopus 로고    scopus 로고
    • A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
    • Hemminki A., Markie D., Tomlinson I., et al. A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Nature 391 (1998) 184-187
    • (1998) Nature , vol.391 , pp. 184-187
    • Hemminki, A.1    Markie, D.2    Tomlinson, I.3
  • 46
    • 0031974516 scopus 로고    scopus 로고
    • Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase
    • Jenne D.E., Reimann H., Nezu J., et al. Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase. Nat Genet 18 (1998) 38-43
    • (1998) Nat Genet , vol.18 , pp. 38-43
    • Jenne, D.E.1    Reimann, H.2    Nezu, J.3
  • 47
    • 33745966059 scopus 로고    scopus 로고
    • LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome
    • Volikos E., Robinson J., Aittomaki K., et al. LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome. J Med Genet 43 (2006) e18
    • (2006) J Med Genet , vol.43
    • Volikos, E.1    Robinson, J.2    Aittomaki, K.3
  • 48
    • 33744828352 scopus 로고    scopus 로고
    • Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome
    • Hearle N.C., Rudd M.F., Lim W., et al. Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome. J Med Genet 43 (2006) e15
    • (2006) J Med Genet , vol.43
    • Hearle, N.C.1    Rudd, M.F.2    Lim, W.3
  • 49
    • 28844507521 scopus 로고    scopus 로고
    • High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome
    • Aretz S., Stienen D., Uhlhaas S., et al. High proportion of large genomic STK11 deletions in Peutz-Jeghers syndrome. Hum Mutat 26 (2005) 513-519
    • (2005) Hum Mutat , vol.26 , pp. 513-519
    • Aretz, S.1    Stienen, D.2    Uhlhaas, S.3
  • 50
    • 18844439886 scopus 로고    scopus 로고
    • STK11 genotyping and cancer risk in Peutz-Jeghers syndrome
    • Schumacher V., Vogel T., Leube B., et al. STK11 genotyping and cancer risk in Peutz-Jeghers syndrome. J Med Genet 42 (2005) 428-435
    • (2005) J Med Genet , vol.42 , pp. 428-435
    • Schumacher, V.1    Vogel, T.2    Leube, B.3
  • 51
    • 0034113361 scopus 로고    scopus 로고
    • Small bowel polyps in Peutz-Jeghers syndrome: management by combined push enteroscopy and intraoperative enteroscopy
    • Pennazio M., and Rossini F.P. Small bowel polyps in Peutz-Jeghers syndrome: management by combined push enteroscopy and intraoperative enteroscopy. Gastrointest Endosc 51 (2000) 304-308
    • (2000) Gastrointest Endosc , vol.51 , pp. 304-308
    • Pennazio, M.1    Rossini, F.P.2
  • 52
    • 0037240247 scopus 로고    scopus 로고
    • Long-term results of polyp clearance by intraoperative enteroscopy in the Peutz-Jeghers syndrome
    • Edwards D.P., Khosraviani K., Stafferton R., and Phillips R.K. Long-term results of polyp clearance by intraoperative enteroscopy in the Peutz-Jeghers syndrome. Dis Colon Rectum 46 (2003) 48-50
    • (2003) Dis Colon Rectum , vol.46 , pp. 48-50
    • Edwards, D.P.1    Khosraviani, K.2    Stafferton, R.3    Phillips, R.K.4
  • 53
    • 0027665246 scopus 로고
    • Familial juvenile polyposis mit prädominanter Magenbeteiligung
    • Höfting J., Pott G., Schrameyer B., et al. Familial juvenile polyposis mit prädominanter Magenbeteiligung. Z Gastroenterol 31 (1993) 480-483
    • (1993) Z Gastroenterol , vol.31 , pp. 480-483
    • Höfting, J.1    Pott, G.2    Schrameyer, B.3
  • 55
    • 0029362966 scopus 로고
    • Malignant potential in intestinal juvenile polyposis syndromes
    • Coburn M.C., Pricolo V.E., DeLuca F.G., et al. Malignant potential in intestinal juvenile polyposis syndromes. Ann Surg Oncol 2 (1995) 386-391
    • (1995) Ann Surg Oncol , vol.2 , pp. 386-391
    • Coburn, M.C.1    Pricolo, V.E.2    DeLuca, F.G.3
  • 56
    • 0021261655 scopus 로고
    • Familial juvenile polyposis coli: increased risk of colorectal cancer
    • Jarvinen H., and Franssila K.O. Familial juvenile polyposis coli: increased risk of colorectal cancer. Gut 25 (1984) 792-800
    • (1984) Gut , vol.25 , pp. 792-800
    • Jarvinen, H.1    Franssila, K.O.2
  • 57
    • 0031673225 scopus 로고    scopus 로고
    • The risk of gastrointestinal carcinoma in familial juvenile polyposis
    • Howe J.R., Mitros F.A., and Summers R.W. The risk of gastrointestinal carcinoma in familial juvenile polyposis. Ann Surg Oncol 5 (1998) 751-756
    • (1998) Ann Surg Oncol , vol.5 , pp. 751-756
    • Howe, J.R.1    Mitros, F.A.2    Summers, R.W.3
  • 59
    • 0027502124 scopus 로고
    • Generalized juvenile polyposis with mixed pattern and gastric cancer
    • Sassatelli R., Bertoni G., Serra L., et al. Generalized juvenile polyposis with mixed pattern and gastric cancer. Gastroenterology 104 (1993) 910-915
    • (1993) Gastroenterology , vol.104 , pp. 910-915
    • Sassatelli, R.1    Bertoni, G.2    Serra, L.3
  • 60
    • 0024496159 scopus 로고
    • Juvenile polyposis: a case with early presentation and death attributable to adenocarcinoma of the pancreas
    • Walpole I.R., and Cullity G. Juvenile polyposis: a case with early presentation and death attributable to adenocarcinoma of the pancreas. Am J Med Genet 32 (1989) 1-8
    • (1989) Am J Med Genet , vol.32 , pp. 1-8
    • Walpole, I.R.1    Cullity, G.2
  • 61
    • 0031960959 scopus 로고    scopus 로고
    • A gene for familial juvenile polyposis maps to chromosome 18q21.1
    • Howe J.R., Ringold J.C., Summers R.W., et al. A gene for familial juvenile polyposis maps to chromosome 18q21.1. Am J Hum Genet 62 (1998) 1129-1136
    • (1998) Am J Hum Genet , vol.62 , pp. 1129-1136
    • Howe, J.R.1    Ringold, J.C.2    Summers, R.W.3
  • 62
    • 0034972978 scopus 로고    scopus 로고
    • Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis
    • Howe J.R., Bair J.L., Sayed M.G., et al. Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis. Nat Genet 28 (2001) 184-187
    • (2001) Nat Genet , vol.28 , pp. 184-187
    • Howe, J.R.1    Bair, J.L.2    Sayed, M.G.3
  • 63
    • 0034829630 scopus 로고    scopus 로고
    • Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes
    • Zhou X.P., Woodford-Richens K., Lehtonen R., et al. Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes. Am J Hum Genet 69 (2001) 704-711
    • (2001) Am J Hum Genet , vol.69 , pp. 704-711
    • Zhou, X.P.1    Woodford-Richens, K.2    Lehtonen, R.3
  • 64
    • 32944463750 scopus 로고    scopus 로고
    • Mutation screening in juvenile polyposis syndrome
    • Pyatt R.E., Pilarski R., and Prior T.W. Mutation screening in juvenile polyposis syndrome. J Mol Diagn 8 (2006) 84-88
    • (2006) J Mol Diagn , vol.8 , pp. 84-88
    • Pyatt, R.E.1    Pilarski, R.2    Prior, T.W.3
  • 65
    • 27744511296 scopus 로고    scopus 로고
    • Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis
    • Sweet K., Willis J., Zhou X.P., et al. Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis. JAMA 294 (2005) 2465-2473
    • (2005) JAMA , vol.294 , pp. 2465-2473
    • Sweet, K.1    Willis, J.2    Zhou, X.P.3
  • 67
    • 0031831731 scopus 로고    scopus 로고
    • PTEN and inherited hamartoma-cancer syndromes
    • Eng C., and Peacocke M. PTEN and inherited hamartoma-cancer syndromes. Nat Genet 19 (1998) 223
    • (1998) Nat Genet , vol.19 , pp. 223
    • Eng, C.1    Peacocke, M.2
  • 68
    • 0036664427 scopus 로고    scopus 로고
    • Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers
    • Friedl W., Uhlhaas S., Schulmann K., et al. Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers. Hum Genet 111 (2002) 108-111
    • (2002) Hum Genet , vol.111 , pp. 108-111
    • Friedl, W.1    Uhlhaas, S.2    Schulmann, K.3
  • 69
    • 25644432127 scopus 로고    scopus 로고
    • Vessels' morphology in SMAD4 and BMPR1A-related juvenile polyposis
    • Handra-Luca A., Condroyer C., de Moncuit C., et al. Vessels' morphology in SMAD4 and BMPR1A-related juvenile polyposis. Am J Med Genet 138 (2005) 113-117
    • (2005) Am J Med Genet , vol.138 , pp. 113-117
    • Handra-Luca, A.1    Condroyer, C.2    de Moncuit, C.3
  • 70
    • 0033738748 scopus 로고    scopus 로고
    • Will the real Cowden syndrome please stand up: revised diagnostic criteria
    • Eng C. Will the real Cowden syndrome please stand up: revised diagnostic criteria. J Med Genet 37 (2000) 828-830
    • (2000) J Med Genet , vol.37 , pp. 828-830
    • Eng, C.1
  • 71
    • 13944265646 scopus 로고    scopus 로고
    • The hamartomatous polyposis syndromes: a clinical and molecular review
    • Schreibman I.R., Baker M., Amos C., and McGarrity T.J. The hamartomatous polyposis syndromes: a clinical and molecular review. Am J Gastroenterol 100 (2005) 476-490
    • (2005) Am J Gastroenterol , vol.100 , pp. 476-490
    • Schreibman, I.R.1    Baker, M.2    Amos, C.3    McGarrity, T.J.4
  • 72
    • 0035011886 scopus 로고    scopus 로고
    • Hamartomatous polyposis syndromes: molecular genetics, neoplastic risk, and surveillance recommendations
    • Wirtzfeld D.A., Petrelli N.J., and Rodriguez-Bigas M.A. Hamartomatous polyposis syndromes: molecular genetics, neoplastic risk, and surveillance recommendations. Ann Surg Oncol 8 (2001) 319-327
    • (2001) Ann Surg Oncol , vol.8 , pp. 319-327
    • Wirtzfeld, D.A.1    Petrelli, N.J.2    Rodriguez-Bigas, M.A.3
  • 73
    • 19144370572 scopus 로고    scopus 로고
    • Genetic mapping of the hereditary mixed polyposis syndrome to chromosome 6q
    • Thomas H.J.W., Whitelaw S.C., Cottrell S.E., et al. Genetic mapping of the hereditary mixed polyposis syndrome to chromosome 6q. Am J Hum Genet 58 (1996) 770-776
    • (1996) Am J Hum Genet , vol.58 , pp. 770-776
    • Thomas, H.J.W.1    Whitelaw, S.C.2    Cottrell, S.E.3
  • 74
    • 0033067274 scopus 로고    scopus 로고
    • Inherited susceptibility to colorectal adenomas and carcinomas: evidence for a new predisposition gene on 15q14-q22
    • Tomlinson I., Rahman N., Frayling I., et al. Inherited susceptibility to colorectal adenomas and carcinomas: evidence for a new predisposition gene on 15q14-q22. Gastroenterology 116 (1999) 789-795
    • (1999) Gastroenterology , vol.116 , pp. 789-795
    • Tomlinson, I.1    Rahman, N.2    Frayling, I.3
  • 75
    • 0037730140 scopus 로고    scopus 로고
    • An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome
    • Jaeger E.E.M., Woodford-Richens K.L., Lockett M., et al. An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome. Am J Hum Genet 72 (2003) 1261-1267
    • (2003) Am J Hum Genet , vol.72 , pp. 1261-1267
    • Jaeger, E.E.M.1    Woodford-Richens, K.L.2    Lockett, M.3
  • 76
    • 33746806391 scopus 로고    scopus 로고
    • Mapping of hereditary mixed polyposis syndrome (HMPS) to chromosome 10q23 by genomewide high-density single nucleotide polymorphism (SNP) scan and identification of BMPR1A loss of function
    • Cao X., Eu K.W., Kumarasinghe M.P., and Li H.H. Mapping of hereditary mixed polyposis syndrome (HMPS) to chromosome 10q23 by genomewide high-density single nucleotide polymorphism (SNP) scan and identification of BMPR1A loss of function. J Med Genet 43 (2006) e13
    • (2006) J Med Genet , vol.43
    • Cao, X.1    Eu, K.W.2    Kumarasinghe, M.P.3    Li, H.H.4
  • 78
    • 33745752975 scopus 로고    scopus 로고
    • Hyperplastic polyposis syndrome: phenotypic presentations and the role of MBD4 and MYH
    • Chow E., Lipton L., Lynch E., et al. Hyperplastic polyposis syndrome: phenotypic presentations and the role of MBD4 and MYH. Gastroenterology 131 (2006) 30-39
    • (2006) Gastroenterology , vol.131 , pp. 30-39
    • Chow, E.1    Lipton, L.2    Lynch, E.3
  • 79
    • 33645094924 scopus 로고    scopus 로고
    • Hyperplastic polyposis coli syndrome and colorectal carcinoma
    • Rubio C.A., Stemme S., Jaramillo E., and Lindblom A. Hyperplastic polyposis coli syndrome and colorectal carcinoma. Endoscopy 38 (2006) 266-270
    • (2006) Endoscopy , vol.38 , pp. 266-270
    • Rubio, C.A.1    Stemme, S.2    Jaramillo, E.3    Lindblom, A.4
  • 80
    • 7044223112 scopus 로고    scopus 로고
    • Phenotypic characteristics and risk of cancer development in hyperplastic polyposis: case series and literature review
    • Ferrandez A., Samowitz W., DiSario J.A., and Burt R.W. Phenotypic characteristics and risk of cancer development in hyperplastic polyposis: case series and literature review. Am J Gastroenterol 99 (2004) 2012-2018
    • (2004) Am J Gastroenterol , vol.99 , pp. 2012-2018
    • Ferrandez, A.1    Samowitz, W.2    DiSario, J.A.3    Burt, R.W.4
  • 81
    • 13144252218 scopus 로고    scopus 로고
    • Hyperplastic polyposis and the risk of colorectal cancer
    • Hyman N.H., Anderson P., and Blasyk H. Hyperplastic polyposis and the risk of colorectal cancer. Dis Colon Rectum 47 (2004) 2101-2104
    • (2004) Dis Colon Rectum , vol.47 , pp. 2101-2104
    • Hyman, N.H.1    Anderson, P.2    Blasyk, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.