Results 121 to 130 of about 5,377 (175)

Lobular endocervical glandular hyperplasia diagnosed during surveillance for Peutz-Jeghers Syndrome: A case report. [PDF]

Gynecol Oncol Rep
Ichinose T, Takasaki K, Takahashi Y, Hirano M, Nishida H, Hiraike H, Sasajima Y, Nagasaka K.   +7 more
europepmc   +1 more source

Gastric-type endocervical adenocarcinoma in situ as the presenting feature in a mosaic STK11 pathogenic variant carrier with a Peutz-Jeghers syndrome child. [PDF]

Fam Cancer
Jiang A, Ye Y, Tan H, Tao X, Ma F, Wang H, Xu C, Kang Y.   +7 more
europepmc   +1 more source

Aggressive Colorectal Signet Ring Cell Carcinoma Arising in Peutz-Jeghers Syndrome: A Rare Case of Missed Surveillance with Successful Multimodal Therapy. [PDF]

Eur J Case Rep Intern Med
Hoang CM, Hai YD, Thi MN, Dong HD.
europepmc   +1 more source

Peutz-Jeghers syndrome in women with jejunojejunal intussusception and multiple gastrointestinal polyposis: A case report. [PDF]

Int J Surg Case Rep
Shrestha S, Bhatta BR, Shrestha M, Thapa KS.   +3 more
europepmc   +1 more source

Peutz Jegher syndrome.

Indian pediatrics, 2015
Abhijit, Dutta, Sudip Kumar, Ghosh, Sujit Kumar, Kundu   +2 more
openaire   +1 more source

Rare large sigmoid hamartomatous polyp in an elderly patient with atypical Peutz-Jeghers syndrome: A case report. [PDF]

World J Gastrointest Surg
Tian ZS, Ma XP, Ruan HX, Yang Y, Zhao YL.   +4 more
europepmc   +1 more source

Intestinal occlusion revealing Peutz Jeghers syndrome: A rare case report. [PDF]

Int J Surg Case Rep
Mabrouk MY, Guelil A, Bouzayan L, Slimi Y, Jabi R, Bouziane M.   +5 more
europepmc   +1 more source

[Peutz-Jeghers syndrome].

Vestnik khirurgii imeni I. I. Grekova, 1976
openaire   +1 more source

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Peutz-Jeghers syndrome

Current Opinion in Gastroenterology, 2021
Purpose of review Peutz-Jeghers syndrome is a rare, autosomal dominant, hereditary polyposis syndrome defined by gastrointestinal hamartomas and mucocutaneous pigmentations, caused by a germline mutation in the serine/ threonine kinase 11 or liver kinase B1 (STK11/LKB1) genes.
Ilja, Tacheci, Marcela, Kopacova, Jan, Bures   +2 more
openaire   +2 more sources

Peutz-Jeghers Syndrome

JAMA Dermatology, 2022
This case report describes multiple dark-brown 1- to 2-mm hyperpigmented macules on the lips, nose, and conjunctivae.
Eri, Sato, Takao, Goto, Hitoshi, Honda
openaire   +2 more sources