Glioblastoma multiforme as a manifestation of Turcot's syndrome;Glioblastoma multiforme als manifestation des Turcot-syndroms

Nervenarzt

Volumn 73, Issue 2, 2002, Pages 177-182

  Grips, E ^a,c   Wentzensen, N ^a,b   Sutter, C ^b   Sedlaczek, O ^a   Gebert, J ^b   Weigel, R ^a   Schwartz, A ^a   Von Knebel Doeberitz, M ^b   Hennerici, M ^a  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

^c UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

Glioblastoma multiforme; HNPCC; Turcot's syndrome

Indexed keywords

ADENOMATOUS POLYP; ADULT; ANAMNESIS; ARTICLE; CASE REPORT; CLINICAL FEATURE; COLON CARCINOMA; DIAGNOSTIC TEST; FAMILIAL ADENOMATOUS POLYPOSIS; GLIOBLASTOMA; HEREDITARY NONPOLYPOSIS COLON CARCINOMA; HUMAN; MOLECULAR BIOLOGY; MUTAGENESIS; TURCOT SYNDROME; BASE MISPAIRING; BRAIN TUMOR; COLORECTAL TUMOR; FEMALE; GENETICS; MIDDLE AGED; PEDIGREE; SYNDROME; TEMPORAL LOBE;

CARRIER PROTEIN; MICROSATELLITE DNA; MLH1 PROTEIN, HUMAN; NUCLEAR PROTEIN; TUMOR PROTEIN;

BASE PAIR MISMATCH; BRAIN NEOPLASMS; CARRIER PROTEINS; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; FEMALE; GLIOBLASTOMA; HUMANS; MICROSATELLITE REPEATS; MIDDLE AGED; NEOPLASM PROTEINS; NUCLEAR PROTEINS; PEDIGREE; SYNDROME; TEMPORAL LOBE;

EID: 0036483031     PISSN: 00282804     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00115-001-1233-8     Document Type: Article

References (25)

1. Boland CR, Thibodeau SN, Hamilton SR et al. (1998) A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res 58:5248-57
2. Burke W, Petersen G, Lynch P et al. (1997) Recommendations for follow-up care of individuals with an inherited predisposition to cancer. I. Hereditary nonpolyposis colon cancer. Cancer Genetics Studies Consortium. Jama 277:915-9
3. De Rosa, M, Fasano C, Panariello L et al. (2000) Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene. Oncogene 19: 1719-23
4. Giovannucci E, Egan KM, Hunter DJ et al. (1995) Aspirin and the risk of colorectal cancer in women. N Engl J Med 333: 609-14
5. Hamilton SR, Liu B, Parsons RE et al. (1995) The molecular basis of Turcot's syndrome. N Engl J Med 332: 839-47
6. Herrera (1990) Familial colorectal cancer. Alan R. Liss, New York
7. Kihana T, Fujioka T, Hamada K et al. (1998) Association of replication error positive phenotype with lymphocyte infiltration in endometrial cancers. Jpn J Cancer Res 89: 895-902
8. Kolodner RD, Hall NR, Lipford J et al. (1994) Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations. Genomics 24:516-26
9. Kolodner RD, Hall NR, Lipford J et al. (1995) Structure of the human MLH1 locus and analysis of a large hereditary nonpolyposis colorectal carcinoma kindred for mlh1 mutations. Cancer Res 55:242-8
10. Lal G, Gallinger S (2000) Familial adenomatous polyposis. Semin Surg Oncol 18: 314-323
11. Lynch HT, Lynch JF (2000) Hereditary nonpolyposis colorectal cancer. Semin Surg Oncol 18: 305-313
12. Lynch HT (1996) Is there a role for prophylactic subtotal colectomy among hereditary non-polyposis colorectal cancer germline mutation carriers? [editorial]. Dis Colon Rectum 39: 109-10
13. Lynch HT, Smyrk T (1996) Hereditary non-polyposis colorectal cancer (Lynch syndrome) An updated review. Cancer 78: 1149-67
14. Miyaki M, Nishio J, Konishi M et al. (1997) Drastic genetic instability of tumors and normal tissues in Turcot syndrome. Oncogene 15: 2877-81
15. Myrhoj T, Bisgaard ML, Bernstein I, Svendsen LB, Sondergaard JO, Bulow S (1997) Hereditary non-polyposis colorectal cancer: clinical features and survival. Results from the Danish HNPCC register. Scand J Gastroenterol 32: 572-6
16. Paraf F, Jothy S, Van Meir EG (1997) Brain tumor-polyposis syndrome: two genetic diseases? J Clin Oncol 15: 2744-2758
17. Sutter C, Gebert J, Bischoff P, Herfarth C, von Knebel Doeberitz M (1999) Molecular screening of potential HNPCC patients using a multiplex microsatellite PCR system. Mol Cell Probes 13: 157-65
18. Thun MJ, Namboodiri MM, Heath CW (1991) Aspirin use and reduced risk of fatal colon cancer. N Engl J Med 325: 1593-6
19. Turcot J, Despres JP, St Pierre F (1959) Malignant tumors of the central nervous sytem associated with familial polyposis of the colon: report of two cases. Dis Colon Rectum 2: 465-468
20. Vasen HF, Mecklin JP, Khan PM (1991) The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC). Dis Colon Rectum 35: 424-5
21. Vasen HF, Sanders EA, Taal BG et al. (1996) The risk of brain tumours in hereditary non-polyposis colorectal cancer (HNPCC) Int J Cancer 65: 422-425
22. Vasen HF, Offerhaus GJ, den Hartog Jager FC et al. (1990) The tumour spectrum in hereditary non-polyposis colorectal cancer: a study of 24 kindreds in the Netherlands. Int J Cancer 46: 31-4
23. Vasen HF, Watson P, Mecklin JP, Lynch HT(1999) New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC. Gastroenterology 116: 1453-6
24. Watson P, Lynch HT (1993) Extracolonic cancer in hereditary nonpolyposis colorectal cancer. Cancer 71: 677-85
25. Watson P, Lin KM, Rodriguez-Bigas MA et al. (1998) Colorectal carcinoma survival among hereditary nonpolyposis colorectal carcinoma family members. Cancer 83: 259-66