Familial exocrine carcinoma of the pancreas;Das familiare exokrine Pankreaskarzinom

Deutsche Medizinische Wochenschrift

Volumn 122, Issue 12, 1997, Pages 378-382

  Bartsch, D ^a   Rothmund, M ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CANCER RISK; FAMILIAL CANCER; HUMAN; PANCREAS; PANCREAS CARCINOMA; REVIEW; GENETICS; PANCREAS TUMOR; RISK FACTOR; SYNDROME;

HUMANS; PANCREATIC NEOPLASMS; RISK FACTORS; SYNDROME;

EID: 0030945969     PISSN: 00120472     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1047625     Document Type: Review

References (53)

1. Aarnio, M., J.-P. Mecklin, L. A. Aaltonen, M. Nyström-Lahti, H. J. Järvinen: Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndrome. Int. J. Cancer 64 (1995), 430-433.
2. Bartsch, D., D. W. Shevlin, M. P. Callery, M. Rothmund, S. A. Wells Jr., P. J. Goodfellow: Weitere Untersuchungen zur Bedeutung von Mutationen im Tumorsuppressorgen CDKN2 beim Adenokarzinom des Pankreas. Langenbecks Arch. Chir., Suppl. 1 (1996), 185-189.
3. Bergmann, W., P. Watson, J. de Jong, H. T. Lynch, R. M. Fusaro: Systemic cancer and the FAMMM syndrome. Brit. J. Cancer 61 (1990), 932-936.
4. Bergman, W., N.A. Gruis: Letter to the Editor. New Engl. J. Med. 334 (1996), 471.
5. Caldas, C., S. A. Hahn, R. H. Hruban, M. S. Redston, C. J. Yeo, S. E. Kern: Detection of K-Ras mutations in the stool of patients with pancreatic adenocarcinoma and pancreatic ductal hyperplasia. Cancer Res. 54 (1994), 3568-3573.
6. Ciotti, P., P. Stringini, G. Bianchi-Scarra: Familial melanoma and pancreatic cancer. New Engl. J. Med. 334 (1996), 469-470.
7. Comfort, M. W., A. G. Steinberg: Pedigree of a family with hereditary chronic relapsing pancreatitis. Gastroenterology 21 (1952), 54-63.
8. David, K. L., P. Steiner-Grossman: The potential use of tumor registry data in the recognition and prevention of hereditary and familial cancer. N. Y. St. J. Med. 91 (1991), 150-152.
9. Danes, B. S., H. T. Lynch: A familial aggregation of pancreatic cancer: an in vitro study. J. Amer. med. Ass. 247 (1982), 2798-2802.
10. Dat, N. M., S. J. Sontag: Pancreatic carcinoma in brothers. Ann. Intern. Med. 97 (1982), 282.
11. Durbec, J. P., C. Chevilotte, J. M. Bidart: Diet, alcohol, tobacco and risk of cancer of the pancreas: a case-control study. Brit. J. Cancer 43 (1983), 463-470.
12. Ehrenthal, D., L. Haeger, T. Griffin, C. Compton: Familial pancreatic adenocarcinoma in three generations. A case report and review of the literature. Cancer 59 (1987), 1661-1664.
13. Evans, J. P., W. Burke, R. Chen, R. L. Bennett, R. A. Schmidt, E. Patchen Dellinger, M. Kimmey, D. Crispin, T. A. Brentnall, D. R. Byrd: Familial pancreatic adenocarcinoma. Association with diabetes and early molecular diagnosis. Med. Genet. 32 (1995), 330-335.
14. Falk, R. T., L. W. Pickle, E. T. Fontham, P. Correa, J. F. Fraumeni: Lifestyle risk factors for pancreatic cancer in Louisiana: a case-control study. Amer. J. Epidemiol. 128 (1988), 324-336.
15. Friedman, J. M., P. J. Fialkow: Carcinoma of the pancreas in four brothers. Birth defects 12 (1974), 145-150.
16. Ghadirian, P., P. Boyle, A. Simard, J. Baillargeon, P. Maisonneuve, C. Perret: Reported family aggregation of pancreatic cancer within a population-based case-control study in the Francophone community in Montreal. Int. J. Pancreatol. 10 (1991), 183-196.
17. Ghadirian, P., A. Simard, J. Baillargeon: Tobacco, alcohol, and coffee and cancer of the pancreas. Cancer 67 (1991), 2664-2670.
18. INK4a mutations. New Engl. J. Med. 333 (1995), 970-974.
19. Grajower, M. M.: Familial pancreatic cancer. Ann. Intern. Med. 98 (1983), 111.
20. Groden, J., A. Thliveris, W. Samowitz, M. Carlson, L. Gelbert, H. Albertsen, G. Joslyn, J. Stevens, L. Spirio, M. Robertson, L. Sargeant, K. Krapcho, E. Wolff, R. Burt, J. P. Hughes, J. Warrington, J. McPherson, J. Wasmuth, D. Le Paslier, H. Abderrahim, D. Cohen, M. Leppert, R. White: Identification and characterization of the familial adenomatous polyposis gene. Cell 66 (1991), 589-600.
21. Gruis, N. A., L. A. Sandkuijl, P. A. van der Velden, W. Bergmann, R. R. Frants: CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families. Melanoma Research 5 (1995), 169-177.
22. Gruis, N. A., P. A. van der Velden, L. A. Sandkuijl, W. Bergman, R. R. Frants: Homozygotes for the CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds. Nat. Genet. 10 (1995), 351-353.
23. Gullo, L., R. Pezzilli, A. M. Morselli-Labate, the Italian Pancreatic Cancer Group: Diabetes and the risk of pancreatic cancer. New Engl. J. Med. 331 (1994), 81-84.
24. Iguchi, H., K. Sugano, N. Fukayama, H. Ohkura, K. Sadamoto, K. Ohkoshi, Y. Seo, H. Tomoda, A. Funakoshi, H. Wakasugi: Analysis of Ki-ras mutations in the duodenal juice of patients with pancreatic cancer. Gastroenterology 110 (1996), 221-226.
25. Johan, G., A. Offerhaus, F. M. Giardiello, A. J. Krush, S. V. Booker, A. C. Tersmette, N. C. Kelley, S. R. Hamilton: The risk of upper gastrointestinal cancer in familial adenomatous polyposis. Gastroenterology 102 (1992), 1980-1982.
26. Katkhouda, N., J. Moviel: Pancreatic cancer in mother and daughter. Lancet 2 (1986), 747.
27. Kattwinkel, P., A. Lapey, P. A. di Sant' Agnese, W. A. Edwards, M. P. Hufty: Hereditary pancreatitis: three new kindreds and a critical review of the literature. Pediatrics 51 (1973), 55-69.
28. Koch, K.: Erstmals Trendwende der Krebsmortalität in USA. Dtsch. Ärztebl. 93 (1996), B-2478.
29. Li, F. P., J. F. Fraumeni Jr.: Soft tissue sarcomas, breast cancer, and other neoplasmas. A familial syndrome? Ann. Intern. Med. 71 (1969), 747-752.
30. Liu, B., R. Parsons, N. Papadopoulos, N.C. Nicolaides, H. T. Lynch, P. Watson, J. R. Jass, M. Dunlop, A. Wyllie, A. de la Chapelle, S. R. Hamilton, B. Vogelstein, W. Kinzler: Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. Nat. Med. 2 (1996), 169-174.
31. Lowenfels, A. B., P. Maisonneuve, G. Cavallini, R. W. Ammann, P. G. Lankisch, J. R. Andersen, E. P. Dimagno, Ä. Andren-Sandberg, L. Domellöf: Pancreatitis and the risk of pancreatic cancer. New Engl. J. Med. 328 (1993), 1433-1437.
32. Lumadue, J. A., C. A. Griffin, M. Osman, R. H. Hruban: Familial pancreatic cancer and the genetics of pancreatic cancer. Surg. Clin. N. Amer. 75 (1995), 845-855.
33. Lynch, H. T., M. L. Fitzsimmons, T. C. Smyrk: Familial pancreatic cancer. Clinicopathologic study of 18 nuclear families. Amer. J. Gastroenterol. 85 (1990), 54-60.
34. Lynch, H. T.: Cancer and the familiy history trail. N. Y. St. J. Med. 91 (1991), 145-147.
35. Lynch, H. T., L. Fusaro, J. F. Lynch: Familial pancreatic cancer. A family study. Pancreas 7 (1992), 511-515.
36. Lynch, H. T., T. C. Smyrk, P. Watson, S. J. Lanspa, J. F. Lynch, P. M. Lynch, R. J. Cavalieri, C. R. Boland: Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer. An updated review. Gastroenterology 104 (1993), 1535-1549.
37. Lynch, H. T.: Genetics and pancreatic cancer. Arch. Surg. 129 (1994), 266-268.
38. Lynch, H. T., L. Fusaro, T. C. Smyrk, P. Watson, S. Lanspa, J. F. Lynch: Medical genetic study of eight pancreatic cancer prone families. Cancer Invest. 13 (1995), 141-149.
39. McDermott, R. P., P. Kramer: Adenocarcinoma of the pancreas in four siblings. Gastroenterology 65 (1973), 137-139.
40. McKusick, V. A.: Ataxia teleangiectatica. In McKusick, M. A. (Hrsg.): Mendelian inheritance in man, edition 9. (John Hopkins University Press: Baltimore 1990), S 68.
41. Madrazo-de la Garza, J., I. D. Hill, E. Lebenthal: Hereditary pancreatitis. In Go, V. L. (Hrsg.): The Pancreas: Biology, pathobiology, and disease. (Raven Press: New York 1993), S. 1095-1101.
42. Malkin, D., F. P. Li, L. C. Strong, J. F. Fraumeni Jr., C. E. Nelson, D. H. Kim, J. Kassel, M. A. Gryka, F. Z. Bischoff, M. A. Tainsky, S. H. Friend: Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Science 250 (1990), 1233-1238.
43. New York Times: Gloria Carter Spann, President Carters last surviving sib, also suffers from pancreatic cancer. New York Times (1989), 1. Dezember.
44. Rakhov, P. A.: Malignant tumor of the pancreas in two sisters. Quest. Oncol. 22 (1976), 90-92.
45. Reimer, R. R., J. F. Fraumeni, R. F. Ozols, R. Bender: Pancreatic cancer in father and son. Lancet 1 (1977), 911-912.
46. Robert-Koch-Institut: Geschätzte Zahl der Neuerkrankungen nach Krebsarten in Deutschland 1993. Robert-Koch-Institut-Schriften 2 (1995).
47. Savitsky, K., A. Bar-Shira, S. Gilad, G. Rotman, Y. Ziv, L. Vanagaite, D. A. Tagle, S. Smith, T. Uziel, M. Lovett, F. S. Collins, Y. Shiloh: A single ataxia teleangiectasia gene with a product similar to Pl-3 Kinase. Science 268 (1995), 1749-1753.
48. Silverman, D. T., L. M. Brown, R. N. Hoover, M. Schiffman, K. D. Liooemoe, J. B. Schoenberg, G. M. Swanson, R. B. Hayes, R. S. Greenberg, J. Benichou, A. G. Schwartz, J. M. Liff, L. M. Pottern: Alcohol and pancreatic cancer in blacks and whites in the United States. Cancer Res. 55 (1995), 4899-4905.
49. Tada, M., M. Omata, S. Kawai, H. Saisho, M. Ohto, R. K. Saiki, J. J. Sninsky: Detection of ras gene mutations in pancreatic juice and peripheral blood of patients with pancreatic adenocarcinoma. Cancer Res. 53 (1993), 2472-2764.
50. Watanabe, H., N. Sawabu, Y. Songür, Y. Yamaguchi, O. Yamakawa, Y. Satomura, H. Ohta, Y. Motoo, T. Okai, T. Wakabayashi: Detection of K-ras point mutations at codon 12 in pure pancreatic juice for the diagnosis of pancreatic cancer by PCR-RFLP analysis. Pancreas 12 (1996), 18-24.
51. Whelan, A. J., D. Bartsch, P. J. Goodfellow: A familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene. New Engl. J. Med. 333 (1995), 975-977.
52. Whelan, A. J., D. Bartsch, P. J. Goodfellow: Letter to the Editor. New Engl. J. Med. 334 (1996), 472.
53. INK4a allele. J. Nat. Canc. Inst. 88 (1996), 1489-1491.