|
1
|
Peutz JLA: Very remarkable case of
familial polyposis of mucous membrane of intestinal tract and
nasopharynx accompanied by peculiar pigmentations of skin and
mucous membrane. Nederl Maandschr Geneesk. 10:134–146. 1921.(In
Dutch).
|
|
2
|
Jeghers H, McKusick VA and Katz KH:
Generalized intestinal polyposis and melanin spots of the oral
mucosa, lips and digits: A syndrome of diagnostic significance. N
Engl J Med. 241:993–1005. 1949. View Article : Google Scholar
|
|
3
|
Ueki A, Kisu I, Banno K, et al:
Gynecological tumors in patients with Peutz-Jeghers syndrome (PJS).
OJGen. 1:65–69. 2011. View Article : Google Scholar
|
|
4
|
Buck JL, Harned RK, Lichtenstein JE and
Sobin LH: Peutz-Jeghers syndrome. Radiographics. 12:365–378. 1992.
View Article : Google Scholar : PubMed/NCBI
|
|
5
|
Gatalica Z and Torlakovic E: Pathology of
hereditary colorectal carcinoma. Fam Cancer. 7:15–26. 2008.
View Article : Google Scholar
|
|
6
|
Hirasawa A, Akahane T, Tsuruta T, et al:
Lobular endocervical glandulara hyperplasia and peritoneal
pigmentation associated with Peutz-Jeghers syndrome due to a
germline mutation of STK11. Annal Oncol. 23:2990–2992. 2012.
View Article : Google Scholar : PubMed/NCBI
|
|
7
|
Tanwar PS, Kaneko-Tarui T, Zhang L, Tanaka
Y, Crum CP and Teixeira JM: Stromal liver kinase B1 [STK11]
signaling loss induces oviductal adenomas and endometrial cancer by
activating mammalian target of rapamycin complex 1. PLoS Genet.
8:e10029062012.PubMed/NCBI
|
|
8
|
Ito M, Minaguchi M, Mikami Y, Ueda Y,
Sekiyama K, Yamamoto T and Takakura K: Peutz-Jeghers
syndrome-associated atypical mucinous proliferation of the uterine
cervix: a case of minimal deviation adenocarcinoma (‘adenoma
malignum’) in situ. Pathol Res Pract. 208:623–627. 2012.PubMed/NCBI
|
|
9
|
Tsuji T, Togami S, Nomoto M, Higashi M,
Fukukura Y, Kamio M, Yonezawa S and Douchi T: Uterine cervical
carcinomas associated with loblar endocervical glandular
hyperplasia. Histopathology. 59:55–62. 2011. View Article : Google Scholar : PubMed/NCBI
|
|
10
|
Koo YJ, Lee JE, Hong SR and Kwon YS:
Co-occurrence of an adenoma malignum and an endocervical-type
adenocarcinoma of the uterine cervix in a woman with Peutz-Jeghers
syndrome. J Gynecol Oncol. 21:203–206. 2010. View Article : Google Scholar : PubMed/NCBI
|
|
11
|
Clements A, Robison K, Granai C, Steinhoff
NM, Scalia-Wibur J and Moore RG: A case of Peutz-Jeghers syndrome
with breast, bilateral sex cord tumor with annular tubules, and
adenoma malgnum caused by STK11 gene mutation. Int J Gynecol
Cancer. 19:1591–1594. 2009. View Article : Google Scholar : PubMed/NCBI
|
|
12
|
Papp J, Kovacs ME, Solyom S, et al: High
prevalence of germline STK11 mutations in Hungarian Peutz-Jeghers
Syndrome patients. BMC Med Genet. 11:1692010. View Article : Google Scholar : PubMed/NCBI
|
|
13
|
Hemminki A, Tomlinson I, Markie D, et al:
Localization of a susceptibility locus for Peutz-Jeghers syndrome
to 19p using comparative genomic hybridization and targeted linkage
analysis. Nat Genet. 15:87–90. 1997. View Article : Google Scholar : PubMed/NCBI
|
|
14
|
Amos CI, Bali D, Thiel TJ, et al: Fine
mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome
19p. Cancer Res. 57:3653–3656. 1997.PubMed/NCBI
|
|
15
|
Jenne DE, Reimann H, Nezu J, et al:
Peutz-Jeghers syndrome is caused by mutations in a novel serine
threonine kinase. Nat Genet. 18:38–43. 1998. View Article : Google Scholar : PubMed/NCBI
|
|
16
|
Buchet-Poyau K, Mehenni H, Radhakrishna U
and Antonarakis SE: Search for the second Peutz-Jeghers syndrome
locus: exclusion of STK13, PRKCG, KLK10, and PSCD2 genes on
chromosome 19 and the STK11IP gene on chromosome 2. Cytogenet
Genome Res. 97:171–178. 2002. View Article : Google Scholar : PubMed/NCBI
|
|
17
|
Yoon KA, Ku JL, Choi HS, et al: Germline
mutations of the STK11 gene in Korean Peutz-Jeghers syndrome
patients. Br J Cancer. 82:1403–1406. 2000.PubMed/NCBI
|
|
18
|
Tseng CJ, Chen SF, Liou SI, et al: Lack of
STK11 gene expression in homozygous twins with Peutz-Jeghers
syndrome. Ann Clin Lab Sci. 34:154–158. 2004.PubMed/NCBI
|
|
19
|
Souza J, Faucz F, Sotomaior V, Filho AB,
Rosenfeld J and Raskin S: Chromosome 19p13.3 deletion in a child
with Peutz-Jeghers syndrome, congenital heart defect, high myopia,
learning difficulties and dysmorphic features: Clinical and
molecular characterization of a new contiguous gene syndrome. Genet
Mol Biol. 34:557–561. 2011. View Article : Google Scholar
|
|
20
|
Scollon S, McWalter K, Abe K, King J,
Kimata K and Slavin TP: Haploinsufficiency of STK11 and neighboring
genes cause a contiguous gene syndrome including Peutz-Jeghers
phenotype. Am J Med Genet A. 158A:2959–2962. 2012. View Article : Google Scholar : PubMed/NCBI
|
|
21
|
Scully RE: Sex cord tumor with annular
tubules: a distinctive ovarian tumor of the Peutz-Jeghers syndrome.
Cancer. 25:1107–1121. 1970. View Article : Google Scholar : PubMed/NCBI
|
|
22
|
Young RH, Welch WR, Dickersin GR and
Scully RE: Ovarian sex cord tumor with annular tubules: Review of
74 cases including 27 with Peutz-Jeghers syndrome and four with
adenoma malignum of the cervix. Cancer. 50:1384–1402. 1982.
View Article : Google Scholar : PubMed/NCBI
|
|
23
|
Silverberg SG and Hurt WG: Minimal
deviation adenocarcinoma (‘adenoma malignum’) of the cervix : a
reappraisal. Am J Obstet Gynecol. 121:971–975. 1975.
|
|
24
|
Nucci MR, Clement PB and Young RH: Lobular
endocervical glandular hyperplasia, not otherwise specified: a
clinicopathologic analysis of thirteen cases of a distinctive
pseudoneoplastic lesion and comparison with fourteen cases of
adenoma malignum. Am J Surg Pathol. 23:886–891. 1999. View Article : Google Scholar
|
|
25
|
Connolly DC, Katabuchi H, Cliby WA and Cho
KR: Somatic mutations in the STK11/LKB1 gene are uncommon in rare
gynecological tumor types associated with Peutz-Jegher’s syndrome.
Am J Pathol. 156:339–345. 2000.PubMed/NCBI
|
|
26
|
Nishioka Y, Kobayashi K, Sagae S, et al:
Mutational analysis of STK11 gene in ovarian carcinomas. Jpn J
Cancer Res. 90:629–632. 1999. View Article : Google Scholar : PubMed/NCBI
|
|
27
|
Kuragaki C, Enomoto T, Ueno Y, et al:
Mutations in the STK11 gene characterize minimal deviation
adenocarcinoma of the uterine cervix. Lab Invest. 83:35–45. 2003.
View Article : Google Scholar : PubMed/NCBI
|
|
28
|
Lee JY, Dong SM, Kim HS, et al: A distinct
region of chromosome 19p13.3 associated with the sporadic form of
adenoma malignum of the uterine cervix. Cancer Res. 58:1140–1143.
1998.PubMed/NCBI
|
|
29
|
Hemminki A, Markie D, Tomlinson I, et al:
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome.
Nature. 391:184–187. 1998. View
Article : Google Scholar : PubMed/NCBI
|
|
30
|
Nakagawa H, Koyama K, Miyoshi Y, et al:
Nine novel germline mutations of STK11 in ten families with
Peutz-Jeghers syndrome. Hum Genetics. 103:168–172. 1998. View Article : Google Scholar : PubMed/NCBI
|
|
31
|
Gilks CB, Young RH, Aguirre P, DeLellis RA
and Scully RE: Adenoma malignum (minimal deviation adenocarcinoma)
of the uterine cervix: A clinicopathological and
immunohistochemical analysis of 26 cases. Am J Surg Pathol.
13:717–729. 1989. View Article : Google Scholar : PubMed/NCBI
|
|
32
|
Kaminski PF and Norris HJ: Minimal
deviation carcinoma (adenoma malignum) of the cervix. Int J Gynecol
Pathol. 2:141–152. 1983. View Article : Google Scholar : PubMed/NCBI
|
|
33
|
von Hochstetter AR, Ess D, Bannwart F and
Bühler H: Adenocarcinoma of the cervix in Peutz-Jeghers syndrome.
Case report and review of the literature. Schweiz Med Wochenschr.
117:1910–1914. 1987.(In German).
|
|
34
|
Giardiello FM, Brensinger DJ, Tersmette
AC, et al: Very high risk of cancer in familial Peutz-Jeghers
syndrome. Gastroenterology. 119:1147–1153. 2000. View Article : Google Scholar : PubMed/NCBI
|
|
35
|
Banno K, Kisu I, Yanokura M, et al:
Epigenetics and genetics in endometrial cancer: new carcinogenic
mechanisms and relationship with clinical practice. Epigenomics.
4:147–162. 2012. View Article : Google Scholar : PubMed/NCBI
|
|
36
|
Boardman LA, Thibodeau SN, Schaid DJ, et
al: Increased risk for cancer in patients with the Peutz-Jeghers
syndrome. Ann Intern Med. 128:896–899. 1998. View Article : Google Scholar : PubMed/NCBI
|
|
37
|
Mangili G, Taccagni G, Garavaglia E,
Carnelli M and Montoli S: An unusual admixture of neoplastic and
metaplastic lesions of the female genital tract in the
Peutz-Jeghers syndrome. Gynecol Oncol. 92:337–342. 2004. View Article : Google Scholar : PubMed/NCBI
|
