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Clinco-pathologic Features of Alopecia in a Patient of Cronkhite-Canada Syndrome

Seong GH, Shon U, Park MJ, Park M, Hong SP, Kim MH, Park BC

  • KMID: 2457691
  • Korean J Dermatol.
  • 2019 Aug;57(7):391-394.
Although hair loss in Cronkhite-Canada syndrome (CCS) developed frequently, its exact mechanism has not been elucidated. Thus, we attempted to investigate the histopathologic features of hair loss with scalp biopsy...
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Cronkhite-Canada Syndrome Showing Good Early Response to Steroid Treatment

Cho W, Nam K, Bang KB, Shin HD, Shin JE

No abstract available.
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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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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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Chemopreventive Action of Anthocyanin-rich Black Soybean Fraction in APC(Min/+) Intestinal Polyposis Model

Park MY, Kim JM, Kim JS, Choung MG, Sung MK

BACKGROUND: Anthocyanins have been shown to inhibit cancer cell growth by suppressing oxidative stress and inflammatory responses. The purpose of this study was to investigate the effects of an anthocyanin-rich...
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Pathogenesis and Management of Serrated Polyps: Current Status and Future Directions

Anderson J

Hyperplastic or serrated polyps were once believed to have little to no clinical significance. A subset of these polyps are now considered to be precursors to colorectal cancers (CRC) in...
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Cronkhite-Canada Syndrome Associated with Serrated Adenoma and Malignant Polyp: A Case Report and a Literature Review of 13 Cronkhite-Canada Syndrome Cases in Korea

Yun SH, Cho JW, Kim JW, Kim JK, Park MS, Lee NE, Lee JU, Lee YJ

Cronkhite-Canada syndrome (CCS) is a rare nonfamilial polyposis syndrome characterized by epithelial disturbances both in the gastrointestinal tract and in the epidermis. The pathologic finding of the polyp is usually...
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A Novel Germline Mutation in Exon 10 of the SMAD4 Gene in a Familial Juvenile Polyposis

Jee MJ, Yoon SM, Kim EJ, Choi HJ, Kim JW, Sung RH, Han JH, Chae HB, Park SM, Youn SJ

  • KMID: 1712337
  • Gut Liver.
  • 2013 Nov;7(6):747-751.
Familial juvenile polyposis (FJP) is a rare autosomal dominant hereditary disorder that is characterized by the development of multiple distinct juvenile polyps in the gastrointestinal tract and an increased risk...
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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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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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A Case of Cronkhite-Canada Syndrome with Esophageal Candidiasis

Park MS, Jung YJ, Oh KJ, Sim JS, Kang DG, Jung EJ, Shin HS, Shin WG

Cronkhite-Cadana syndrome is a rare non-familial disease. This syndrome is characterized by multiple hamartomatous polyps on the entire gastrointestinal tract except esophagus, nail dystrophy, alopecia and hyperpigmentation. Taste disturbance, abdominal...
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Peutz-Jeghers Syndrome: A Case Report and Review of Literature

Kim HS, Kim SM, Choi JY, Myoung H, Lee SK, Lee JH

  • KMID: 1434398
  • J Korean Assoc Maxillofac Plast Reconstr Surg.
  • 2012 Sep;34(5):363-366.
Peutz-Jeghers syndrome is a rare syndrome with characteristic features of multiple hamartomatous polyps and mucocutaneous pigmentation. This syndrome is an autosomal dominant disease, and has complications related with polyps of...
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Role of Enhanced Visibility in Evaluating Polyposis Syndromes Using a Newly Developed Contrast Image Capsule Endoscope

Hatogai K, Hosoe N, Imaeda H, Rey JF, Okada S, Ishibashi , Kimura K, Yoneno K, Usui S, Ida Y, Tsukada N, Kanai T, Hibi T, Ogata H

  • KMID: 2284267
  • Gut Liver.
  • 2012 Apr;6(2):218-222.
BACKGROUND/AIMS: A flexible spectral imaging color enhancement system was installed in new capsule software for video capsule endoscopy. Contrast image capsule endoscopy (CICE) is a novel technology using light-emitting diodes...
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A Case of Cronkhite-Canada Syndrome Presenting with Hematochezia

Lee HJ, Park SJ, Choi HS, Keum B, Seo YS, Kim YS, Jeen YT, Lee HS, Chun HJ, Um SH, Kim CD, Ryu HS

Cronkhite-Canada syndrome (CCS) is a rare, non-familial hamartomatous polyposis syndrome characterized by multiple polyps in the entire gastrointestinal tract, nail dystrophy, skin pigmentation, and systemic alopecia. The clinical symptoms of...
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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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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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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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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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A Case of Cronkhite-Canada Syndrome Conducted with Capsule Endoscopy of Small Intestine

Park W, Jeon WK, Lee JE, Choi WS, Seo MH, Yoon MY, Song CS, Kim DH

  • KMID: 1454598
  • Korean J Gastrointest Endosc.
  • 2010 Feb;40(2):126-129.
Cronkhite-Canada syndrome is a very rare syndrome. This non-familial hamartomatous polyposis syndrome is characterized by multiple polyps on the entire gastrointestinal tract, nail dystrophy, skin pigmentation and systemic alopecia. The...
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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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