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Serrated Polyposis Syndrome with a Synchronous Colon Adenocarcinoma Treated by an Endoscopic Mucosal Resection

Lee SH, Lee SJ, Park SC, Nam SJ, Kang MH, Kim TS, Lee SK

Serrated polyposis syndrome (SPS) can transform to malignant lesions through the sessile serrated pathway and traditional serrated pathway. These pathways may cause rapid neoplastic progression compared to the adenoma-carcinoma sequence,...
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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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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 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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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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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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Long-term Follow-up of a Case of Cowden Syndrome

Choi SY, Kim HS, Park KS, Lee HJ, Oh HK, Hwang JB

  • KMID: 1979848
  • Korean J Pediatr Gastroenterol Nutr.
  • 2004 Mar;7(1):112-118.
Cowden syndrome is very rare clinical condition with characteristic mucocutaneous lesions associated with abnormalities of the breast, thyroid, and gastrointestinal tract. Here, the case of a 16-year-old girl with diverse...
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A Case of Cowden's Syndrome

Chun CH, Jung SA, Cho YK, Lee N, Yeoum MS, Chang JE, Shin JE, Ju MS, Sung Y, Yoo K, Moon IH

  • KMID: 2243425
  • Korean J Gastrointest Endosc.
  • 2002 Jan;24(1):17-20.
A 17-year-old man was referred to our hospital because of dizziness and mild dyspnea. He had a history of partial thyroidectomy due to benign mass when he was 10 year-old....
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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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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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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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