- Peutz-Jeghers syndrome: a new understanding
-
Choi HS, Park YJ, Park JG
- KMID: 1062189
- J Korean Med Sci.
- 1999 Feb;14(1):2-7.
- doi: 10.3346/jkms.1999.14.1.2
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... -
- CITED
-
- Close
- SHARE
-
- Close
- Peutz-Jeghers Syndrome with Recurrent Intussusception
-
Lee MJ, Kim JH, Hwang Y
- KMID: 2325075
- J Korean Surg Soc.
- 2005 Jul;69(1):88-91.
The Peutz-Jeghers syndrome is an autosomal dominant hereditary disease characterized by hamartomatous polyps of the gastrointestinal tract and by mucocutaneous melanin deposits. This syndrome is clinically important because of the... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Peutz-Jegher's Syndrome
-
Chung CS, Huh W
- KMID: 2039203
- Korean J Dermatol.
- 1970 Jul;8(2):79-82.
A case of Peutz-Jeghers syndrome was experienced with melanin pigmentation in the oral cavity and lips associated small intestine polyposis. Diagnosis of Peutz-Jeghers syndrome was established by clinical characteristics of... -
- CITED
-
- Close
- SHARE
-
- Close
- The surgical point of Peutz-Jeghers syndrome
-
Lee SH, Jung PM
- KMID: 2143788
- Korean J Gastroenterol.
- 1992 Dec;24(6):1260-1266.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Hamartomatous Polyp without Peutz-Jeghers Syndrome Arising from Appendix
-
Sohn WS, Park JS, Kim JE, Kim BH, Yoo SH, Han EM
- KMID: 2243108
- Korean J Gastrointest Endosc.
- 2010 Jul;41(1):36-40.
Peutz-Jeghers syndrome is a familial syndrome consisting of mucocutaneous pigmentation and gastrointestinal polyposis and appears to be inherited as a single pleiotropic autosomal dominant gene with variable and incomplete penetrance.... -
- CITED
-
- Close
- SHARE
-
- Close
- Two Cases of a Solitary Peutz-Jeghers Polyp in the Rectum
-
You IY, Youn SJ, Jeon WJ, Ko B, Chae HB, Park SM, Lee HC
- KMID: 1494814
- Korean J Gastrointest Endosc.
- 2008 Feb;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... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Peutz-Jeghers Syndrome
-
Park I, Oh S, Ko J, Byun S, Choeh K
- KMID: 1682873
- J Korean Pediatr Soc.
- 1989 Jul;32(7):990-994.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Bilateral Breast Cancers arising in Peutz-Jeghers Syndrome Patient: A Case Report
-
Son YM, Kim EK, Kim MJ, Moon HJ
- KMID: 1704984
- J Korean Soc Ultrasound Med.
- 2013 Sep;32(3):212-215.
Peutz-Jeghers syndrome is an unusual autosomal dominant disorder characterized by gastrointestinal hamartomatous polyps, mucocutaneous pigmentation, and a variety of intestinal and extra-intestinal malignancies. Incidence of breast and gynecologic malignancies is... -
- CITED
-
- Close
- SHARE
-
- Close
- Two Cases of Peutz-Jeghers Syndrome
-
Sul JH, Kim KC, Kim BS
- KMID: 1663615
- J Korean Pediatr Soc.
- 1978 Jul;21(7):557-562.
Familial association of gastrointestinal polyposis with mucocutaneous pigmentation was first reportde by Peutz in 1921. Following reemphsis by Jeghers in 1949, it became a definite clinical disease entity known as... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Peutz-Jeghers Syndrome with Intussusception
-
Ko KH, Lee KJ, Park SY, Kim HJ, Hahm KB, Kim JH, Cho SW, Jin YM, Lee TS
- KMID: 1537281
- Korean J Gastrointest Endosc.
- 2000 Jan;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... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of a Solitary Peutz-Jeghers Type Hamartomatous Polyp in the Duodenum with Upper Gastrointestinal Bleeding as the Initial Diagnosis
-
Lee JH, Lee CR, Choi SJ, Kim WS, Lee DS, Han SR, Park HS, Choi SH, Lee HJ
- KMID: 2084220
- Korean J Gastrointest Endosc.
- 1999 Oct;19(5):796-800.
Peutz-Jeghers syndrome is a genetic disorder consisting of mucocutaneous pigmentation and gastrointestinal polyposis. Although the polyp may be found in a solitary fashion in this syndrome, such a case is... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Peutz-Jeghers Syndrome
-
Kim SK, Park CH, Kim JH, Myung KC, Ra CS
- KMID: 1676268
- J Korean Pediatr Soc.
- 1985 Jun;28(6):622-626.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Colon Cancer in Peutz-Jeghers Syndrome
-
Chung WS, Choi HC, Chang TS
- KMID: 2206540
- J Korean Surg Soc.
- 1999 Jul;57(1):131-136.
Peutz-Jeghers syndrome is an autosomal dominant disease characterized by hamartomatous polyps in the gastrointestinal tract and by mucocutaneous melanin pigmentations. The relationship between gastrointestinal polyps and the syndrome has been... -
- CITED
-
- Close
- SHARE
-
- Close
- Two Cases of Peutz-Jeghers Syndrome
-
Moon JS, Jin SK, Moon DS, Cho KS, Cho JD
- KMID: 1677084
- J Korean Pediatr Soc.
- 1987 Aug;30(8):907-915.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Peutz-Jeghers Syndrome with Small Bowel Perforation and Enteritis Cystica Profunda
-
Ahn KS, Bae JD, Kim HG, Shon HS, Choe JY, Kim CH, Kim IG, Kim TS, Kim CG
- KMID: 2084750
- Korean J Gastroenterol.
- 1997 May;29(5):677-682.
The Peutz-Jeghers syndrome is an autosornal dominant condition characterized by mucocutaneous pigmentation and hamartomatous polyps of the gastrointestinal tract. This syndrome is clinically important because of complications caused by gastrointestinal... -
- CITED
-
- Close
- SHARE
-
- Close
- A case of Peutz-Jeghers syndrome combined with prolapsed polyp through anus
-
Yang YS, Cho NC, Yoon KS, Kim DS, Kim SY
- KMID: 1685363
- Korean J Gastroenterol.
- 1992 Feb;24(1):148-153.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- A case of Peutz-Jeghers syndrome associated with jejuno-ideal intussusception
-
Kim SH, Mok WG, Choi JW, Choi JB, So BJ, Joo HZ
- KMID: 1939893
- J Korean Surg Soc.
- 1993 Nov;45(5):900-905.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- A Case Report of Peutz - Jeghers' Syndrome Associated Anemia and Intussusception
-
Lee YG, Kim CH, Choi SW, Moon HS, Jeong JW, Park DH, Kim BS, Seo EJ
- KMID: 2143714
- Korean J Gastrointest Endosc.
- 1989 May;9(1):43-47.
The Peutz-Jeghers syndrome has three cardinal features: gastrointestinal polypasis, mucocutaneous piginentation and autosomal dominant heredity. This syndrome is ciinically important because of the complication caused by the gastrointestinal ployp, leading... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Crohn's Disease Accompanied by Peutz-Jeghers Syndrome
-
Um YJ, Kim SM, Pyo JS, Lee JA, Koo HS, Huh KC
- KMID: 1792744
- Korean J Gastroenterol.
- 2013 Oct;62(4):243-247.
- doi: 10.4166/kjg.2013.62.4.243
Peutz-Jeghers syndrome is an autosomal dominant inherited disorder characterized by multiple gastrointestinal hamartomatous polyps and mucocutaneous pigmentation. Peutz-Jeghers syndrome has an incidence of approximately 1 in 25,000 to 300,000 births.... -
- CITED
-
- Close
- SHARE
-
- Close
- Intraoperative Enteroscopic Total Polypectomy for the Patients with Peutz-Jeghers Syndrome
-
Yoo SB, Kim IY, Sung SH, Kim DS, Rhoe BS
- KMID: 1944728
- J Korean Soc Coloproctol.
- 2004 Dec;20(6):405-410.
Patients with Peutz-Jeghers syndrome often suffer complications of the polyps, such as intussusception, bowel obstruction, and bleeding. Furthermore, repeated operations may be required in some patients, which may result in... -
- CITED
-
- Close
- SHARE
-
- Close
