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Intestinal polyposis

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

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

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

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?

Ko BM

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

Lim MS, Seo JK, Ko JS, Yang HR, Kang GH, Kim WS

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

Koh KJ, Park HN, Kim KA

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

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

Song L, Jhun BW, Park J, Kim D, Chang DK, Kim YH, Kim JJ, Kim JY

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

Ha JW

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?

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

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

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

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

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

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

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

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

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

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

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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