1.Two Cases of Peutz-Jeghers Syndrome.
Joo Saeng MOON ; Sung Ki JIN ; Doo Sung MOON ; Kyung Sook CHO ; Jong Dase CHO
Journal of the Korean Pediatric Society 1987;30(8):907-915
No abstract available.
Peutz-Jeghers Syndrome*
2.Complete STK11 Deletion and Atypical Symptoms in Peutz-Jeghers Syndrome.
Myeong Sun JANG ; Yoo Min LEE ; Bong Min KO ; Goeun KANG ; Jong Won KIM ; Yong Hee HONG
Annals of Laboratory Medicine 2017;37(5):462-464
No abstract available.
Peutz-Jeghers Syndrome*
3.A case report of peutz-jeghers syndrome causing ileocolic intussusception.
Cheong Yong KIM ; Youg Hwan KIM ; Hong Joon CHUN ; Suen Woo BACK ; Young Don MIN ; Chan Gook PARK ; Joo Nam BYUN
Journal of the Korean Society of Coloproctology 1993;9(1):77-82
No abstract available.
Intussusception*
;
Peutz-Jeghers Syndrome*
4.A Case of Peutz-Jeghers Syndrome.
Sang Kie KIM ; Choon Ho PARK ; Jin Heon KIM ; Keun Chul MYUNG ; Chang Soo RA
Journal of the Korean Pediatric Society 1985;28(6):622-626
No abstract available.
Peutz-Jeghers Syndrome*
5.A Case of Peutz-Jeghers Syndrome.
Ickberm PARK ; Sungguen OH ; Jungsuk KO ; Sanghyun BYUN ; Kyuchul CHOEH
Journal of the Korean Pediatric Society 1989;32(7):990-994
No abstract available.
Peutz-Jeghers Syndrome*
6.A case of Peutz-Jeghers syndrome associated with jejuno-ideal intussusception.
Sin Hyung KIM ; Woo Gyun MOK ; Jung Whan CHOI ; Jung Bae CHOI ; Byung Jo SO ; Hoong Zae JOO
Journal of the Korean Surgical Society 1993;45(5):900-905
No abstract available.
Intussusception*
;
Peutz-Jeghers Syndrome*
7.Peutz-Jeghers syndrome: a new understanding.
Hyo Seong CHOI ; Young Jin PARK ; Jae Gahb PARK
Journal of Korean Medical Science 1999;14(1):2-7
Peutz-Jeghers syndrome is an autosomal dominant inherited disorder characterized by hamartomatous polyps in the small bowel and mucocutaneous pigmentation. Patients with Peutz-Jeghers syndrome often present as surgical emergencies with complications of the polyps, such as intussusception, bowel obstruction and bleeding. Furthermore, repeated operations may be needed in some patients, which may result in short bowel syndrome. Although early reports did not demonstrate a predisposition to cancer in patients with this syndrome, more recent studies have described an increased risk for both gastrointestinal and extra-gastrointestinal cancers. Women with the Peutz-Jeghers syndrome have the extremely high risk for breast and gynecologic cancer. Recently, Peutz-Jeghers syndrome susceptibility gene, encoding the serine threonine kinase STK11 (also called LKB1), was identified in families with Peutz-Jeghers syndrome. The identifications of germline mutations in families with Peutz-Jeghers syndrome could be a turning point in the management of Peutz-Jeghers syndrome.
Female
;
Human
;
Neoplasms/etiology
;
Peutz-Jeghers Syndrome*/pathology
;
Peutz-Jeghers Syndrome*/genetics
;
Peutz-Jeghers Syndrome*/complications
;
Phenotype
;
Risk Factors
8.Two Cases of a Solitary Peutz-Jeghers Polyp in the Rectum.
Il Young YOU ; Sei Jin YOUN ; Won Joong JEON ; Byeongseong KO ; Hee Bok CHAE ; Seon Mee PARK ; Ho chang LEE
Korean Journal of Gastrointestinal Endoscopy 2008;36(2):107-111
Peutz-Jeghers syndrome is a rare autosomal dominant disorder in which multiple hamartomatous polyps are present in the gastrointestinal tract in association with distinctive mucocutaneous pigmentation. A single hamartomatous polyp arising in a patient without pigmentation or familial history of Peutz-Jeghers syndrome is termed a solitary Peutz-Jeghers polyp; such a case is rare and would result in a case report being presented even in other countries. We experienced two cases of a solitary Peutz-Jeghers polyp that developed in the rectum, and report the cases with a review of the literature.
Gastrointestinal Tract
;
Humans
;
Peutz-Jeghers Syndrome
;
Pigmentation
;
Polyps
;
Rectum
9.Two Case Reports of Intussusception in Patients with Peutz-Jeghers Syndrome.
Il Ju YOON ; Hyoung Sim SER ; Chan Ho OK
Journal of the Korean Radiological Society 2001;44(5):589-592
Peutz-Jeghers syndrome(PJS) is a relatively rare autosomal-dominant disease characterized by the occurrence of extensive mucocutaneous hyperpigmentation and gastrointestinal polyps. PJS patients are considered to have a high prevalence of intussusception due to polyps. We report the radiological findings in two cases of intussusception due to polyps in patients with PJS, and review the literature.
Humans
;
Hyperpigmentation
;
Intussusception*
;
Peutz-Jeghers Syndrome*
;
Polyps
;
Prevalence
10.A Case of Peutz-Jeghers Syndrome with Intussusception.
Kwang Hyun KO ; Kwang Jae LEE ; So Yune PARK ; Hun Jong KIM ; Ki Baik HAHM ; Jin Hong KIM ; Sung Weon CHO ; Yun Mi JIN ; Tae Seung LEE
Korean Journal of Gastrointestinal Endoscopy 2000;20(1):73-76
Peutz-Jeghers syndrome is a rare autosomal dominant disorder defined by hamartomatous polyps of gastrointestinal tracts and the occurrence of melanin spots on the mucocutaneous surface. This syndrome has important complications such as malignant transformation, gastrointestinal bleeding, and intussusception. About 50% of patients with Peutz-Jeghers syndrome involved Intussusception. A case of Peutz-Jeghers syndrome with intussusception was recently experienced and herein reported.
Gastrointestinal Tract
;
Hemorrhage
;
Humans
;
Intussusception*
;
Melanins
;
Peutz-Jeghers Syndrome*
;
Polyps