Medical management update: Peutz Jeghers syndrome

Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology and Endodontology

Volumn 109, Issue 1, 2010, Pages 5-11

  Higham, Paola ^a   Alawi, Faizan ^a   Stoopler, Eric T ^a  

^a UNIVERSITY OF PENNSYLVANIA SCHOOL OF DENTAL MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 72049111472     PISSN: 10792104     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tripleo.2009.08.022     Document Type: Review

References (72)

1. Giardiello F.M., and Trimbath J.D. Peutz-Jeghers syndrome and management recommendations. Clin Gastroenterol Hepatol 4 4 (2006) 408-415
2. McGarrity T.J., and Amos C. Peutz-Jeghers syndrome: Clinicopathology and molecular alterations. Cell Mol Life Sci 63 18 (2006) 2135-2144
3. Peutz J.L.A. Very remarkable case of familial polyposis of mucous membrane of intestinal tract and nasopharynx accompanied by peculiar pigmentation of skin and mucous membrane. Nederl Maandische Geneesk 10 (1921) 134-146
4. Brassett C., Joyce J.A., Froggatt N.J., Williams G., Furniss D., Walsh S., et al. Microsatellite instability in early onset and familial colorectal cancer. J Med Genet 33 12 (1996) 981-985
5. Mcgrath D.R., and Spigelman A.D. Preventive measures in Peutz-Jeghers syndrome. Fam Cancer 1 2 (2001) 121-125
6. McGarrity T.J., Kulin H.E., and Zaino R.J. Peutz-Jeghers syndrome. Am J Gastroenterol 95 3 (2000) 596-604
7. Burt R.W. Polyposis syndromes. Clin Perspectives Gastroenterol 5 1 (2002) 51-59
8. Boardman L.A. Heritable colorectal cancer syndromes: recognition and preventive management. Gastroenterol Clin North Am 31 4 (2002) 1107-1131
9. Amos C.I., Keitheri-Cheteri M.B., Sabripour M., Wei C., McGarrity T.J., Seldin M.F., et al. Genotype-phenotype correlations in Peutz-Jeghers syndrome. J Med Genet 41 5 (2004) 327-333
10. Kyle J. Peutz-Jeghers syndrome. Scot Med J 6 (1961) 361-367
11. Hemminki A., Avizienyte E., Roth S., Loukola A., Aaltonen L.A., Jar̈vinen H., et al. A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Duodecim 114 7 (1998) 667-668
12. Jenne D.E., Reimann H., Nezu J., Friedel W., Loff S., Jeschke R., et al. Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase. Nat Genet 18 1 (1998) 38-43
13. Wang Z., Ellis I., Zauber P., Iwama T., Marchese C., Talbot I., et al. Allelic imbalance at the LKB1 (STK11) locus in tumors from patients with Peutz-Jeghers' syndrome provides evidence for a hamartoma-(adenoma)-carcinoma sequence. J Pathol 188 1 (1999) 9-13
14. Hemminki A., Tomlinson I., Markie D., Jar̈vinen H., Sistonen P., Bjor̈kqvist A., et al. Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis. Nat Genet 15 1 (1997) 87-90
15. Yoo L.I., Chung D.C., and Yuan J. LKB1-A master tumor suppressor of the small intestine and beyond. Nat Rev Cancer 2 7 (2002) 529-535
16. Le Meur N., Martin C., Saugier-Veber P., Joly G., Lemoine F., Moirot H., et al. Complete germline deletion of the STK11 gene in a family with Peutz-Jeghers syndrome. Eur J Hum Genet 12 5 (2004) 415-418
17. Mehenni H., Gehrig C., Nezu J., Oku A., Shimane M., Rossier C., et al. Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity. Am J Hum Genet 63 6 (1998) 1641-1650
18. Jishage K., Nezu J., Kawase Y., Iwata T., Watanabe M., Miyoshi A., et al. Role of Lkb1, the causative gene of Peutz-Jegher's syndrome, in embryogenesis and polyposis. Proc Natl Acad Sci U S A 99 13 (2002) 8903-8908
19. Olschwang S., Markie D., Seal S., Neale K., Phillips R., Cottrell S., et al. Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3. J Med Genet 35 1 (1998) 42-44
20. Schumacher V., Vogel T., Leube B., Driemel C., Goecke T., Mos̈lein G., et al. STK11 genotyping and cancer risk in Peutz-Jeghers syndrome. J Med Genet 42 5 (2005) 428-435
21. Mehenni H., Blouin J., Radhakrishna U., Bhardwaj S.S., Bhardwaj K., Dixit V.B., et al. Peutz-Jeghers syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus, on 19q13.4. Am J Hum Genet 61 6 (1997) 1327-1334
22. Calva D., and Howe J.R. Hamartomatous polyposis syndromes. Surg Clin N Am 88 4 (2008) 779-817
23. Erbe R.W. Current concepts in genetics. Inherited gastrointestinal polyposis syndromes. New Engl J Med 294 20 (1976) 1101-1104
24. Schreibman I.R., Baker M., Amos C., and McGarrity T.J. The hamartomatous polyposis syndromes: a clinical and molecular review. Am J Gastroenterol 100 2 (2005) 476-490
25. Utsunomiya J., Gocho H., and Miyanaga T. Peutz-Jeghers syndrome: its natural course and management. Johns Hopkins Med J 136 2 (1975) 71-82
26. Aaltonen L.A., Jarvinen H., Gruber S.B., Billaud M., and Jass J.R. Peutz-Jeghers syndrome. In: Hamilton S.R., and Aaltonen L.A. (Eds). Pathology and genetics of tumors of the digestive system (2000), IARC Press, Lyon 74-76
27. Tomlinson I.P.M., and Houlston R.S. Peutz-Jeghers syndrome. J Med Genet 34 12 (1997) 1007-1011
28. Westerman A.M., and Wilson J.H.P. Peutz-Jeghers syndrome: risks of a hereditary condition: a clinical review. Scand J Gastroenterol Suppl 230 (1999) 64-70
29. Wada K., Tanaka M., Yamaguchi K., and Wada K. Carcinoma and polyps of the gallbladder associated with Peutz-Jeghers syndrome. Dig Dis Sci 32 8 (1987) 943-946
30. Costamagna G., Shah S.K., Riccioni M.E., Foschia F., Mutignani M., Perri V., et al. A prospective trial comparing small bowel radiographs and video capsule endoscopy for suspected small bowel disease. Gastroenterol 123 4 (2002) 999-1005
31. 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 7 (2005) 1498-1502
32. May A., Nachbar L., and Ell C. Double-balloon enteroscopy (push-and-pull enteroscopy) of the small bowel: feasibility and diagnostic and therapeutic yield in patients with suspected small bowel disease. Gastrointest Endosc 62 1 (2005) 62-70
33. Pennazio M., Santucci R., Rondonotti E., Abbiati C., Beccari G., Rossini F.P., et al. Outcome of patients with obscure gastrointestinal bleeding after capsule endoscopy: report of 100 consecutive cases. Gastroenterol 126 3 (2004) 643-653
34. Plum N., May A.D., Manner H., and Ell C. Peutz-Jeghers syndrome: endoscopic detection and treatment of small bowel polyps by double-balloon enteroscopy. Zeitschrift fur Gastroenterologie 45 10 (2007) 1049-1055
35. Peutz-Jeghers syndrome. The Johns Hopkins guide for patients and families (2001), Johns Hopkins University, Baltimore
36. Hinds R., Philp C., Hyer W., and Fell J.M. Complications of childhood Peutz-Jeghers syndrome: implications for pediatric screening. J Pediatr Gastroenterol Nutr 39 2 (2004) 219-220
37. Giardiello F.M., Brensinger J.D., Tersmette A.C., Goodman S.N., Petersen G.M., Booker S.V., et al. Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterol 119 6 (2000) 1447-1453
38. Stehling L.C., Doherty D.C., Faust R.J., Greenburg A.G., Harrison C.R., Landers D.F., et al. Practice guidelines for blood component therapy: a report by the American Society of Anesthesiologists task force on blood component therapy. Anesthesiology 84 3 (1996) 732-747
39. Kurugoglu S., Aksoy H., Kantarci F., Cetinkaya S., Mihmanli I., and Korman U. Radiological work-up in Peutz-Jeghers syndrome. Pediatr Radiol 33 11 (2003) 766-771
40. Wei C., Amos C.I., Zhang N., Wang X., Rashid A., Walker C.L., et al. Suppression of Peutz-Jeghers polyposis by targeting mammalian target of rapamycin signaling. Clin Cancer Res 14 4 (2008) 1167-1171
41. Steinbach G., Lynch P.M., Phillips R.K.S., Wallace M.H., Hawk E., Gordon G.B., et al. The effect of celecoxib, a cyclooxygenase-2 inhibitor, in familial adenomatous polyposis. New Engl J Med 342 26 (2000) 1946-1952
42. Herendeen J.M., and Lindley C. Use of NSAIDs for the chemoprevention of colorectal cancer. .Ann Pharmacother 37 11 (2003) 1664-1674
43. Gros̈ch S., Maier T.J., Schiffmann S., and Geisslinger G. Cyclooxygenase-2 (COX-2) - independent anticarcinogenic effects of selective COX-2 inhibitors. J Natl Cancer Inst 98 11 (2006) 736-747
44. Phillips R.K.S., Wallace M.H., Lynch P.M., Hawk E., Gordon G.B., Saunders B.P., et al. A randomized, double blind, placebo controlled study of celecoxib, a selective cyclooxygenase 2 inhibitor, on duodenal polyposis familial adenomatous polyposis. Gut 50 6 (2002) 857-860
45. Chang C., and Nelson J.S. Q-switched ruby laser treatment of mucocutaneous melanosis associated with Peutz-Jeghers syndrome. Ann Plast Surg 36 4 (1996) 394-397
46. Polla L.L., Margolis R.J., and Dover J.S. Melanosomes are a primary target of Q-switched ruby laser irradiation in guinea pig skin. J Invest Dermatol 89 3 (1987) 281-286
47. Dover J.S., Margolis R.J., Polla L.L., Watanabe S., Hruza G.J., Parrish J.A., et al. Pigmented guinea pig skin irradiated with Q-switched ruby laser pulses. Morphologic and histologic findings. Arch Dermatol 125 1 (1989) 43-49
48. Nelson J.S., and Applebaum J. Treatment of superficial cutaneous pigmented lesions by melanin-specific selective photothermolysis using the Q-switched ruby laser. Ann Plast Surg 29 3 (1992) 231-237
49. Geronemus R.G. Q-switched ruby laser therapy of nevus of ota. Arch Dermatol 128 12 (1992) 1618-1622
50. Goldberg D.J. Benign pigmented lesions of the skin: treatment with the Q-switched ruby laser. J Dermatol Surg Oncol 19 4 (1993) 376-379
51. Lowe N.J., Wieder J.M., Sawcer D., Burrows P., and Chalet M. Nevus of ota: treatment with high energy fluences of the Q-switched ruby laser. J Am Acad Dermatol 29 6 (1993) 997-1001
52. Hemminki A. The molecular basis and clinical aspects of Peutz-Jeghers syndrome. Cell Mol Life Sci 55 5 (1999) 735-750
53. Clark S.F. Iron deficiency anemia. Nutr Clin Pract 23 2 (2008) 128-141
54. Handelman G.J., and Levin N.W. Iron and anemia in human biology: a review of mechanisms. Heart Failure Rev 13 4 (2008) 393-404
55. Cantu J.M., Rivera H., and Ocampo-Campos R. Peutz-Jeghers syndrome with feminizing sertoli cell tumor. Cancer 46 1 (1980) 223-228
56. Westerman A.M., Entius M.M., De Baar E., Boor P.P.C., Koole R., Van Velthuysen M.L.F., et al. Peutz-Jeghers syndrome: 78-year follow-up of the original family. Lancet 353 9160 (1999) 1211-1215
57. Konishi F., Wyse N.E., Muto T., Sawada T., Morioka Y., Sugimura H., et al. Peutz-Jeghers polyposis associated with carcinoma of the digestive organs. Report of three cases and review of the literature. Dis Colon Rectum 30 10 (1987) 790-799
58. Ylikorkala A., Avizienyte E., Tomlinson I.P.M., Tiainen M., Roth S., Loukola A., et al. Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer. Hum Mol Genet 8 1 (1999) 45-51
59. Giardiello F.M., Welsh S.B., and Hamilton S.R. Increased risk of cancer in the Peutz-Jeghers syndrome. New Engl J Med 316 24 (1987) 1511-1514
60. Spigelman A.D., Murday V., and Phillips R.K.S. Cancer and the Peutz-Jeghers syndrome. Gut 30 11 (1989) 1588-1590
61. Traboulsi E.I., and Maumenee I.H. Periocular pigmentation in the Peutz-Jeghers syndrome. Am J Ophthalmol 102 1 (1986) 126-127
62. Chaudhry S.I., Philpot N.S., Odell E.W., Challacombe S.J., and Shirlaw P.J. Pyostomatitis vegetans associated with asymptomatic ulcerative colitis. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 87 3 (1999) 327-330
63. Zaheri S., Chong S.K.F., and Harland C.C. Treatment of mucocutaneous pigmentation in Peutz-Jeghers syndrome with potassium titanyl phosphate (KTP) laser [4]. Clin Exp Dermatol 30 6 (2005) 710-712
64. Field E.A., Speechley J.A., Rugman F.R., Varga E., and Tyldesley W.R. Oral signs and symptoms in patients with undiagnosed vitamin B12 deficiency. J Oral Pathol Med 24 10 (1995) 468-470
65. Daley T.D., and Armstrong J.E. Oral manifestations of gastrointestinal diseases. Can J Gastroenterol 21 4 (2007) 241-244
66. Kalaitzakis E., Carlsson E., Josefsson A., and Bosaeus I. Quality of life in short-bowel syndrome: impact of fatigue and gastrointestinal symptoms. Scand J Gastroenterol 43 9 (2008) 1057-1065
67. DeRossi S.S., and Raghavendra S. Anemia. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 95 2 (2003) 131-141
68. Napolitano L.M. Perioperative anemia. Surg Clin North Am 85 6 (2005) 1215-1227
69. Nuttall G.A., Brost B.C., Connis R.T., Gessner J.S., Harrison C.R., Miller R.D., et al. Practice guidelines for perioperative blood transfusion and adjuvant therapies: an updated report by the American Society of Anesthesiologists task force on perioperative blood transfusion and adjuvant therapies. Anesthesiology 105 1 (2006) 198-208
70. Goodnough L.T., Shander A., Spivak J.L., Waters J.H., Friedman A.J., Carson J.L., et al. Detection, evaluation, and management of anemia in the elective surgical patient. Anesth Analg 101 6 (2005) 1858-1861
71. Parekh N.R., and Steiger E. Short bowel syndrome. Curr Treat Options Gastroenterol 10 1 (2007) 10-23
72. Tilg H. Short bowel syndrome: searching for the proper diet. Eur J Gastroenterol Hepatol 20 11 (2008) 1061-1063