Results 171 to 180 of about 10,344 (216)

Ischemic Polypectomy Through Detachable Snare and Rubber Band Ligation in Peutz-Jeghers Syndrome. [PDF]

ACG Case Rep J
Tan JRL, Co JT.
europepmc   +1 more source

Global research landscape of Peutz-Jeghers syndrome and successful endoscopic management of intestinal intussusception in patients with recurrent laparotomies. [PDF]

World J Gastrointest Surg
Sun Q, Wang XY, Guo GJ, Wang L, Meng LM, Guo YF, Sun T, Ning SB.   +7 more
europepmc   +1 more source

Device-assisted enteroscopy in the surveillance of intestinal hamartomas in Peutz-Jeghers syndrome. [PDF]

Endosc Int Open
Mohamed Elfeky OW, Panjwani S, Cave D, Wild D, Raines D.   +4 more
europepmc   +1 more source

Gastric-type endocervical adenocarcinoma, superficial myofibroblastoma, sex cord-stromal tumors, and HSIL in Peutz-Jeghers syndrome: a rare case report, genetic characterization, and review of literature. [PDF]

Front Oncol
Sun D, Li Y, Cao Z.
europepmc   +1 more source

A Case Report of a Young Adult With Peutz-Jeghers Syndrome Presenting With Acute Small Bowel Obstruction: A Common Complication of an Uncommon Disease. [PDF]

Cureus
Kuruvila A, Philip P, Thomas A, Benjamin G.   +3 more
europepmc   +1 more source

[Current research status of Peutz-Jeghers syndrome in children]. [PDF]

Zhongguo Dang Dai Er Ke Za Zhi
Tong Q.
europepmc   +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

PEUTZ‐JEGHERS SYNDROME

Australian and New Zealand Journal of Surgery, 1985
Peutz‐Jeghers syndrome has now been widely reported. A case with previously unrecorded conjunctival pigmentation is presented and the management is reviewed.
P A, Dewan, J K, Hope
openaire   +4 more sources

Peutz-Jeghers syndrome

The American Journal of Gastroenterology, 2000
Peutz-Jeghers syndrome (PJS) is an unusual polyposis syndrome that has enjoyed a rich and somewhat confusing history. Mucocutaneous pigmentation and diffuse gastrointestinal hamartomas are the hallmark features of this autosomal dominant inherited condition. Peutz-Jeghers syndrome is now also recognized as a cancer predisposition syndrome.
T J, McGarrity, H E, Kulin, R J, Zaino
openaire   +4 more sources