Home |
Current Issue |
Past Issues |
In the Clinic |
ACP Journal Club |
CME |
Collections |
Audio/Video |
Mobile |
Subscribe |
Tools |
Help |
ACP Online
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 June 1998 | Volume 128 Issue 11 | Pages 896-899
Background: Some reports describe an increased risk for cancer in patients with the Peutz-Jeghers syndrome.
Objective: To characterize occurrences of cancer in a large cohort of patients with the Peutz-Jeghers syndrome.
Design: Retrospective cohort study.
Setting: Tertiary care center.
Patients: 34 patients with the Peutz-Jeghers syndrome identified from Mayo Clinic records from 1945 to 1996.
Measurements: Cases of cancer documented by chart review and telephone follow-up.
Results: 26 cases of noncutaneous cancer developed in 18 of the 34 patients: 10 cases of gastrointestinal cancer and 16 cases of extraintestinal cancer. With the use of SEER (Surveillance, Epidemiology, and End Results) data for comparison, the relative risk for cancer was 18.5 (95% CI, 8.5 to 35.2) in women with the Peutz-Jeghers syndrome and 6.2 (CI, 2.5 to 12.8) in men with the syndrome (P = 0.001). In women, the relative risk for breast and gynecologic cancer was 20.3 (CI, 7.4 to 44.2).
Conclusions: The Peutz-Jeghers syndrome is associated with an increased risk for cancer. The relative risk for breast and gynecologic cancers is particularly high.
Author and Article Information
From the Mayo Clinic, Rochester, Minnesota. For current author addresses, see end of text.
ARTICLE
Increased Risk for Cancer in Patients with the Peutz-Jeghers Syndrome
![]()
Acknowledgments: The authors thank Ms. Julie A. Tienter and Ms. Gail L. Prechel for manuscript preparation.
Requests for Reprints: Lynn C. Hartmann, MD, Mayo Clinic, 200 First Street SW, Rochester, MN 55905.
Current Author Addresses: Drs. Boardman, Thibodeau, Schaid, Lindor, McDonnell, Burgart, Ahlquist, Podratz, Pittelkow, and Hartmann: Mayo Clinic, 200 First Street SW, Rochester, MN 55905.
This article has been cited by other articles:
![]() |
H. B. Pearson, A. McCarthy, C. M.P. Collins, A. Ashworth, and A. R. Clarke Lkb1 Deficiency Causes Prostate Neoplasia in the Mouse Cancer Res., April 1, 2008; 68(7): 2223 - 2232. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Flutter and R. Mulik Peutz-Jegher syndrome Arch. Dis. Child., February 1, 2008; 93(2): 163 - 163. [Full Text] [PDF] |
||||
![]() |
W. W J de Leng, A. M. Westerman, M. A J Weterman, M. Jansen, H. van Dekken, F. M Giardiello, F. W M de Rooij, J H Paul Wilson, G J. A Offerhaus, and J. J Keller Nasal polyposis in Peutz-Jeghers syndrome: a distinct histopathological and molecular genetic entity J. Clin. Pathol., April 1, 2007; 60(4): 392 - 396. [Abstract] [Full Text] [PDF] |
||||
![]() |
H Mehenni, N Resta, J-G Park, M Miyaki, G Guanti, and M C Costanza Cancer risks in LKB1 germline mutation carriers Gut, July 1, 2006; 55(7): 984 - 990. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Wei, C. I. Amos, L. C. Stephens, I. Campos, J. M. Deng, R. R. Behringer, A. Rashid, and M. L. Frazier Mutation of Lkb1 and p53 Genes Exert a Cooperative Effect on Tumorigenesis Cancer Res., December 15, 2005; 65(24): 11297 - 11303. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Nanda, L. P. Schumm, S. Cummings, J. D. Fackenthal, L. Sveen, F. Ademuyiwa, M. Cobleigh, L. Esserman, N. M. Lindor, S. L. Neuhausen, et al. Genetic Testing in an Ethnically Diverse Cohort of High-Risk Women: A Comparative Analysis of BRCA1 and BRCA2 Mutations in American Families of European and African Ancestry JAMA, October 19, 2005; 294(15): 1925 - 1933. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Mehenni, N. Lin-Marq, K. Buchet-Poyau, A. Reymond, M. A. Collart, D. Picard, and S. E. Antonarakis LKB1 interacts with and phosphorylates PTEN: a functional link between two proteins involved in cancer predisposing syndromes Hum. Mol. Genet., August 1, 2005; 14(15): 2209 - 2219. [Abstract] [Full Text] [PDF] |
||||
![]() |
V Schumacher, T Vogel, B Leube, C Driemel, T Goecke, G Moslein, and B Royer-Pokora STK11 genotyping and cancer risk in Peutz-Jeghers syndrome J. Med. Genet., May 1, 2005; 42(5): 428 - 435. [Full Text] [PDF] |
||||
![]() |
A R Brooks-Wilson, P Kaurah, G Suriano, S Leach, J Senz, N Grehan, Y S N Butterfield, J Jeyes, J Schinas, J Bacani, et al. Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria J. Med. Genet., July 1, 2004; 41(7): 508 - 517. [Abstract] [Full Text] [PDF] |
||||
![]() |
C I Amos, M B Keitheri-Cheteri, M Sabripour, C Wei, T J McGarrity, M F Seldin, L Nations, P M Lynch, H H Fidder, E Friedman, et al. Genotype-phenotype correlations in Peutz-Jeghers syndrome J. Med. Genet., May 1, 2004; 41(5): 327 - 333. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. L. Thull and V. G. Vogel Recognition and Management of Hereditary Breast Cancer Syndromes Oncologist, February 1, 2004; 9(1): 13 - 24. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Wei, C. I. Amos, A. Rashid, M. Sabripour, L. Nations, T. J. McGarrity, and M. L. Frazier Correlation of Staining for LKB1 and COX-2 in Hamartomatous Polyps and Carcinomas from Patients with Peutz-Jeghers Syndrome J. Histochem. Cytochem., December 1, 2003; 51(12): 1665 - 1672. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Ghaffar, F. Sahin, M. Sanchez-Cepedes, G. H. Su, M. Zahurak, D. Sidransky, and W. H. Westra LKB1 Protein Expression in the Evolution of Glandular Neoplasia of the Lung Clin. Cancer Res., August 1, 2003; 9(8): 2998 - 3003. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. A. Hahn, B. Greenhalf, I. Ellis, M. Sina-Frey, H. Rieder, B. Korte, B. Gerdes, R. Kress, A. Ziegler, J. A. Raeburn, et al. BRCA2 Germline Mutations in Familial Pancreatic Carcinoma J Natl Cancer Inst, February 5, 2003; 95(3): 214 - 221. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Marschall and P. Hayes Intussusceptions in a man with Peutz-Jeghers syndrome Can. Med. Assoc. J., February 4, 2003; 168(3): 315 - 316. [Full Text] [PDF] |
||||
![]() |
D. J. Rossi, A. Ylikorkala, N. Korsisaari, R. Salovaara, K. Luukko, V. Launonen, M. Henkemeyer, A. Ristimaki, L. A. Aaltonen, and T. P. Makela Induction of cyclooxygenase-2 in a mouse model of Peutz-Jeghers polyposis PNAS, September 17, 2002; 99(19): 12327 - 12332. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Hirano, Y. Takiguchi, H. Igari, K. Hiroshima, M. Shingyoji, R. Watanabe, T. Moriya, N. Tanabe, K. Tatsumi, and T. Kuriyama A Case of Pulmonary Adenocarcinoma Accompanied by Superior Vena Caval Thrombosis in a Patient with Peutz-Jeghers Syndrome Jpn. J. Clin. Oncol., August 1, 2002; 32(8): 307 - 309. [Abstract] [Full Text] [PDF] |
||||
![]() |
M M de Jong, I M Nolte, G J te Meerman, W T A van der Graaf, J C Oosterwijk, J H Kleibeuker, M Schaapveld, and E G E de Vries Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility J. Med. Genet., April 1, 2002; 39(4): 225 - 242. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Sato, C. Rosty, M. Jansen, N. Fukushima, T. Ueki, C. J. Yeo, J. L. Cameron, C. A. Iacobuzio-Donahue, R. H. Hruban, and M. Goggins STK11/LKB1 Peutz-Jeghers Gene Inactivation in Intraductal Papillary-Mucinous Neoplasms of the Pancreas Am. J. Pathol., December 1, 2001; 159(6): 2017 - 2022. [Abstract] [Full Text] [PDF] |
||||
![]() |
E EFTHIMIOU, T CRNOGORAC-JURCEVIC, N R LEMOINE, and T A BRENTNALL Inherited predisposition to pancreatic cancer Gut, February 1, 2001; 48(2): 143 - 147. [Full Text] [PDF] |
||||
![]() |
M M Entius, J J Keller, A M Westerman, B P van Rees, M-L F van Velthuysen, A F P M de Goeij, J H P Wilson, F M Giardiello, and G J A Offerhaus Molecular genetic alterations in hamartomatous polyps and carcinomas of patients with Peutz-Jeghers syndrome J. Clin. Pathol., February 1, 2001; 54(2): 126 - 131. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. A. Stratakis, T. Papageorgiou, A. Premkumar, S. Pack, L. S. Kirschner, S. E. Taymans, Z. Zhuang, W. H. Oelkers, and J. A. Carney Ovarian Lesions in Carney Complex: Clinical Genetics and Possible Predisposition to Malignancy J. Clin. Endocrinol. Metab., November 1, 2000; 85(11): 4359 - 4366. [Abstract] [Full Text] |
||||
![]() |
H. F. A. Vasen Clinical Diagnosis and Management of Hereditary Colorectal Cancer Syndromes J. Clin. Oncol., November 1, 2000; 18(90001): 81s - 92. [Full Text] [PDF] |
||||
![]() |
L F Forster, S Defres, D R Goudie, D U Baty, and F A Carey An investigation of the Peutz-Jeghers gene (LKB1) in sporadic breast and colon cancers J. Clin. Pathol., October 1, 2000; 53(10): 791 - 793. [Abstract] [Full Text] [PDF] |
||||
![]() |
J Trojan, A Brieger, J Raedle, M Esteller, and S Zeuzem 5'-CpG island methylation of the LKB1/STK11 promoter and allelic loss at chromosome 19p13.3 in sporadic colorectal cancer Gut, August 1, 2000; 47(2): 272 - 276. [Abstract] [Full Text] [PDF] |
||||
![]() |
A.-M. Martin and B. L. Weber Genetic and Hormonal Risk Factors in Breast Cancer J Natl Cancer Inst, July 19, 2000; 92(14): 1126 - 1135. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Launonen, E. Avizienyte, A. Loukola, P. Laiho, R. Salovaara, H. Järvinen, J.-P. Mecklin, A. Oku, M. Shimane, H. C. Kim, et al. No Evidence of Peutz-Jeghers Syndrome Gene LKB1 Involvement in Left-sided Colorectal Carcinomas Cancer Res., February 1, 2000; 60(3): 546 - 548. [Abstract] [Full Text] |
||||
![]() |
D. C. Connolly, H. Katabuchi, W. A. Cliby, and K. R. Cho Somatic Mutations in the STK11/LKB1 Gene Are Uncommon in Rare Gynecological Tumor Types Associated with Peutz-Jegher’s Syndrome Am. J. Pathol., January 1, 2000; 156(1): 339 - 345. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. H. Su, R. H. Hruban, R. K. Bansal, G. S. Bova, D. J. Tang, M. C. Shekher, A. M. Westerman, M. M. Entius, M. Goggins, C. J. Yeo, et al. Germline and Somatic Mutations of the STK11/LKB1 Peutz-Jeghers Gene in Pancreatic and Biliary Cancers Am. J. Pathol., June 1, 1999; 154(6): 1835 - 1840. [Abstract] [Full Text] [PDF] |
||||