- Intestinal polyposis
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Chang MS, Kim YI
- KMID: 1685257
- Korean J Gastroenterol.
- 1991 Feb;23(1):62-74.
No abstract available. -
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- Laugier-Hunziker Syndrome
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Jang KA, Ahn SJ, Choi JH, Sung KJ, Moon KC, Koh JK
- KMID: 1548210
- Korean J Dermatol.
- 1999 Jan;37(1):108-110.
Laugier-Hunziker syndrone is a rare, pigmentary disorder of the lips, oral mucosa, and nails. The absence of intestinal polyposis differentiated it from Peutz-Jeghers syndrome. We describe a 16-year-old boy with... -
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- A Case of Juvenile Polyposis Syndrome with Whole Gastrointestinal Tract Involvement
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Kim KH, Jeen YT, Keum B, Nam SJ, Park JY, Song JG, Oh CR, Choi WS
- KMID: 1467098
- Korean J Gastrointest Endosc.
- 2009 Jan;38(1):43-46.
Juvenile Polyposis Syndrome is a rare condition that is characterized by the development of multiple polyps in the gastrointestinal tract. It is a hamartomatous disorder that was first described in... -
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- Two Cases of Peutz-Jeghers Syndrome
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Byun DK, Suhl SK, Nam YJ
- KMID: 1663793
- Korean J Dermatol.
- 1965 Aug;4(1):57-61.
Two cases of Feutz-Jeghers Syndrome which showed typical muco-cutaneous pigmentations were reported and the literatures were reviewed. The case 1 was 9 years old boy, who began to have his... -
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- Small Bowel Tumors and Polyposis: How to Approach and Manage?
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Ko BM
- KMID: 2429943
- Korean J Gastroenterol.
- 2018 Dec;72(6):277-280.
- doi: 10.4166/kjg.2018.72.6.277
Although small bowel the mainly occupies the most part of the gastrointestinal tract, small intestine tumors are rare, insidious in clinical presentation, and frequently represent a diagnostic and management challenge.... -
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- Clinical, Endoscopic and Pathologic Findings of Colonic Polyposis in Korean Children
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Lim MS, Seo JK, Ko JS, Yang HR, Kang GH, Kim WS
- KMID: 1459431
- Korean J Pediatr Gastroenterol Nutr.
- 2010 Sep;13(2):154-163.
- doi: 10.5223/kjpgn.2010.13.2.154
PURPOSE: Colonic polyposis is less common in children than in adults. The clinical data pertaining to colonic polyposis in children are limited. Children with colonic polyposis have complications associated with... -
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- Gardner syndrome associated with multiple osteomas, intestinal polyposis, and epidermoid cysts
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Koh KJ, Park HN, Kim KA
- KMID: 2362745
- Imaging Sci Dent.
- 2016 Dec;46(4):267-272.
- doi: 10.5624/isd.2016.46.4.267
Gardner syndrome is known as a variant of familial adenomatous polyposis. This syndrome is characterized by multiple intestinal polyposes, osteomas, and epidermoid cysts. In addition, dental abnormalities include an increased... -
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- Familial Juvenile Polyposis
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Chang SH, Lee SN, Koo HS, Kim OK, Jung SS, Park EB
- KMID: 1725224
- Korean J Pathol.
- 1997 Feb;31(2):185-188.
Familial juvenile polyposis is a rare intestinal polyposis characterized by the occurrence of multiple juvenile polyps in the gastrointestinal tract. We report a case of familial juvenile polyposis in a... -
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- A Case of Cap Polyposis Complicated with Idiopathic Retroperitoneal Fibrosis
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Song L, Jhun BW, Park J, Kim D, Chang DK, Kim YH, Kim JJ, Kim JY
- KMID: 1026370
- Korean J Gastroenterol.
- 2011 Nov;58(5):275-279.
- doi: 10.4166/kjg.2011.58.5.275
An optimal treatment for cap polyposis has not been established. Several treatment approaches, including anti-inflammatory agents, antibiotics, immunomodulators, and endoscopic therapy have been described. Surgical resection of the affected colon... -
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- Autosomal Dominant Inherited Cowden's Disease in a Family
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Ha JW
- KMID: 1792646
- Clin Endosc.
- 2013 Jan;46(1):85-90.
- doi: 10.5946/ce.2013.46.1.85
Cowden's disease, also known as a kind of phosphatase and tensin homolog (PTEN) hamartoma tumor syndrome, is an uncommon autosomal dominant inherited complex disorder with various hamartomatous growths of multiple... -
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- Is Colonoscopy Necessary in Children Suspected of Having Colonic Polyps?
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Lee HJ, Lee JH, Lee JS, Choe YH
- KMID: 1974132
- Gut Liver.
- 2010 Sep;4(3):326-331.
BACKGROUND/AIMS: The clinical spectrum, histology, and endoscopic features of colonic polyps in the pediatric age group were studied to evaluate the role of colonoscopy in children suspected of having colonic... -
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- Two Cases of Cronkhite - Canada Syndrome with Remission
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Kim HJ, Jeen YT, Chun HJ, Hur BW, Kim YS, Park JH, Chun HR, Kang CD, Lee JW, Song CW, Um SH, Kim CD, Ryu HS, Hyun JH
- KMID: 1865462
- Korean J Gastrointest Endosc.
- 2000 Jul;21(1):543-548.
The Cronkhite-Canada Syndrome (CCS) is a monfamilial disorder of adults characterized by diffuse gastro-intestinal polyposis, ectodermal changes consisting of alopecia, dystrophy of nails and cutaneous hyper-pigmentation. The pathogenesis and the... -
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- A Case of Cronkhite-Canada Syndrome Showing Spontaneous Remission
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Kang DU, Yang DH, Choi Y, Kim JB, Lee HS, Lee HJ, Park SH, Jung KW, Kim KJ, Ye BD, Byeon JS, Myung SJ, Yang SK, Kim JH
- KMID: 2284922
- Intest Res.
- 2013 Oct;11(4):317-322.
- doi: 10.5217/ir.2013.11.4.317
Cronkhite-Canada syndrome (CCS) is a rare, noninherited gastrointestinal polyposis syndrome associated with ectodermal changes such as alopecia, nail dystrophy, and cutaneous hyperpigmentation. The etiology and pathogenesis of CCS are not... -
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- Unresectable Desmoid Tumor Developing after Surgery of F.A.P Case report
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Lee HS, Jeon HM, Ok ST, Kim JS, Lee EJ, Kim JS
- KMID: 2025977
- J Korean Soc Coloproctol.
- 1998 Jun;14(2):323-329.
Desmoid tumors are defined as aggressive overgrowth of fibrous sheets and musculoaponeurotic structures. Although desmoid tumors are generally known as a benign neoplasm, it's aggresive local invasiveness and frequent recurrence... -
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- Cronkhite-Canada Syndrome That Developed in a Patient Taking Levothyroxine Sodium after Total Thyroidectomy
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Baek JH, Kim TY
- KMID: 2146309
- Korean J Dermatol.
- 2011 Jan;49(1):45-49.
Cronkhite-Canada Syndrome (CCS) is a rare, non-inherited hamartomatous polyposis syndrome. It is characterized by diffuse gastrointestinal polyposis, diarrhea, weight loss and unique ectodermal manifestations such as alopecia, onychodystrophy and cutaneous... -
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- Usefulness of Capsule Endoscopy in Children with Suspected Small Bowel Disease
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Park HJ, Lee SY, Ko JS, Seo JK
- KMID: 1466929
- Korean J Gastrointest Endosc.
- 2009 Dec;39(6):346-351.
BACKGROUND/AIMS: The aim of our study is to investigate the diagnostic value and safety of capsule endoscopy (CE) in the pediatric patients with small bowel (SB) disease. METHODS: We retrospectively reviewed... -
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- Hereditary Colorectal Cancer
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Park JG, Kim IJ
- KMID: 2439741
- Korean J Gastroenterol.
- 2005 Feb;45(2):78-87.
Hereditary syndromes cause approximately 5 to 15% of overall colorectal cancer (CRC) cases. Hereditary CRC is conventionally divided into two major categories: hereditary non-polyposis colorectal cancer (HNPCC) and those related... -
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- A Case of Cronkhite-Canada Syndrome with a Remission to Steroid Therapy
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Goo YS, Shin HJ, Park JY, Park MC, Lee YC, Kim WH, Park IS, Kim HG, Shin MS
- KMID: 2304908
- Korean J Gastrointest Endosc.
- 2001 Aug;23(2):113-117.
Cronkhite-Canada syndrome is characterized by generalized gastrointestinal polyposis, ectodermal changes, and the eventual development of diarrhea and weight loss. The pathogenesis of the disease is unknown, and there is no... -
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- A Case of Cronkhite-Canada Syndrome
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Chung ST, Chung EC, Choi JH, Sung KJ, Moon KC, Koh JK
- KMID: 1548114
- Korean J Dermatol.
- 1999 Mar;37(3):381-385.
The Cronkhite-Canada syndrome is a rare, non-neoplastic, non-hereditary condition which consists of gastrointestinal polyposis associated with alopecia, onychodystrophy and hyperpigmentation of the skin. It usually encountered with severe diarrhea, weight... -
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- A case ofr Cronkhite-Canada syndrome
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Choi MS, Kim YT, Jung HC, Lee HS, Yoon YB, Song IS, Choi KW, Kim CY
- KMID: 1685364
- Korean J Gastroenterol.
- 1992 Feb;24(1):154-159.
No abstract available. -
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