Cargando…
Cronkhite-Canada syndrome: a rare case report and literature review
BACKGROUND: Cronkhite-Canada Syndrome (CCS) is a rare non-inherited disease characterized by gastrointestinal polyposis and ectodermal abnormalities, the estimated incidence is about one per million. Recognizing and curing the disorder face great challenge. CASE PRESENTATION: This report refers to a...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766628/ https://www.ncbi.nlm.nih.gov/pubmed/26911542 http://dx.doi.org/10.1186/s12876-016-0436-1 |
_version_ | 1782417698849816576 |
---|---|
author | Zhao, Ruifeng Huang, Mely Banafea, Omar Zhao, Jinfang Cheng, Ling Zou, Kaifang Zhu, Liangru |
author_facet | Zhao, Ruifeng Huang, Mely Banafea, Omar Zhao, Jinfang Cheng, Ling Zou, Kaifang Zhu, Liangru |
author_sort | Zhao, Ruifeng |
collection | PubMed |
description | BACKGROUND: Cronkhite-Canada Syndrome (CCS) is a rare non-inherited disease characterized by gastrointestinal polyposis and ectodermal abnormalities, the estimated incidence is about one per million. Recognizing and curing the disorder face great challenge. CASE PRESENTATION: This report refers to a Chinese 52 year old man with gastrointestinal symptoms and ectodermal abnormalities. Gastrointestinal symptoms occurred without obvious cause, followed by ectodermal abnormalities after two months. In several hospitals, endoscopy examinations found numerous polypoid lesions in various sizes spreading over the stomach and the entire colon and rectum, histopathological examinations showed inflammatory and adenomatous polyp. In our hospital, both endoscopy and the contrast-enhanced computed tomography (CT) of small intestine showed gastrointestinal polyposis. Gastric antrum and the colon biopsy samples suggested hyperplastic and inflammatory polyp respectively. Endoscopic ultrasonography (EUS) suggested gastric wall thickening. Fujinnon intelligent color enhancement (FICE) revealed that the size of gastric glands pit varied, and vessels were visible. Confocal endoscope showed increased glandular epithelium layers. Magnifying narrow-band imaging endoscopy (ME-NBI) detected that pit pattern in the mucous of the polyp were regular and type III-IV of microvessels were seen. Biochemical investigations showed anemia, hypoalbuminemia and electrolyte disturbance. IgG, IgA and C3 decreased. Anti-ribosomal phosphoprotein is weak positive. The patient was given nutritional support treatment. Gstrointestinal symptoms and hyperpigmentation improved gradually. CONCLUSION: The patient was ever hospitalized in four hospitals and was diagnosed with CCS after 8 months of gastrointestinal symptoms. So when encountering the patient with gastrointestinal polyposis and ectodermal abnormalities, try to take CCS into consideration. Due to its low incidence, no standard therapy regimen has been established so far. However, nutritional support treatment is of great significance. |
format | Online Article Text |
id | pubmed-4766628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47666282016-02-26 Cronkhite-Canada syndrome: a rare case report and literature review Zhao, Ruifeng Huang, Mely Banafea, Omar Zhao, Jinfang Cheng, Ling Zou, Kaifang Zhu, Liangru BMC Gastroenterol Case Report BACKGROUND: Cronkhite-Canada Syndrome (CCS) is a rare non-inherited disease characterized by gastrointestinal polyposis and ectodermal abnormalities, the estimated incidence is about one per million. Recognizing and curing the disorder face great challenge. CASE PRESENTATION: This report refers to a Chinese 52 year old man with gastrointestinal symptoms and ectodermal abnormalities. Gastrointestinal symptoms occurred without obvious cause, followed by ectodermal abnormalities after two months. In several hospitals, endoscopy examinations found numerous polypoid lesions in various sizes spreading over the stomach and the entire colon and rectum, histopathological examinations showed inflammatory and adenomatous polyp. In our hospital, both endoscopy and the contrast-enhanced computed tomography (CT) of small intestine showed gastrointestinal polyposis. Gastric antrum and the colon biopsy samples suggested hyperplastic and inflammatory polyp respectively. Endoscopic ultrasonography (EUS) suggested gastric wall thickening. Fujinnon intelligent color enhancement (FICE) revealed that the size of gastric glands pit varied, and vessels were visible. Confocal endoscope showed increased glandular epithelium layers. Magnifying narrow-band imaging endoscopy (ME-NBI) detected that pit pattern in the mucous of the polyp were regular and type III-IV of microvessels were seen. Biochemical investigations showed anemia, hypoalbuminemia and electrolyte disturbance. IgG, IgA and C3 decreased. Anti-ribosomal phosphoprotein is weak positive. The patient was given nutritional support treatment. Gstrointestinal symptoms and hyperpigmentation improved gradually. CONCLUSION: The patient was ever hospitalized in four hospitals and was diagnosed with CCS after 8 months of gastrointestinal symptoms. So when encountering the patient with gastrointestinal polyposis and ectodermal abnormalities, try to take CCS into consideration. Due to its low incidence, no standard therapy regimen has been established so far. However, nutritional support treatment is of great significance. BioMed Central 2016-02-25 /pmc/articles/PMC4766628/ /pubmed/26911542 http://dx.doi.org/10.1186/s12876-016-0436-1 Text en © Zhao et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Zhao, Ruifeng Huang, Mely Banafea, Omar Zhao, Jinfang Cheng, Ling Zou, Kaifang Zhu, Liangru Cronkhite-Canada syndrome: a rare case report and literature review |
title | Cronkhite-Canada syndrome: a rare case report and literature review |
title_full | Cronkhite-Canada syndrome: a rare case report and literature review |
title_fullStr | Cronkhite-Canada syndrome: a rare case report and literature review |
title_full_unstemmed | Cronkhite-Canada syndrome: a rare case report and literature review |
title_short | Cronkhite-Canada syndrome: a rare case report and literature review |
title_sort | cronkhite-canada syndrome: a rare case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4766628/ https://www.ncbi.nlm.nih.gov/pubmed/26911542 http://dx.doi.org/10.1186/s12876-016-0436-1 |
work_keys_str_mv | AT zhaoruifeng cronkhitecanadasyndromeararecasereportandliteraturereview AT huangmely cronkhitecanadasyndromeararecasereportandliteraturereview AT banafeaomar cronkhitecanadasyndromeararecasereportandliteraturereview AT zhaojinfang cronkhitecanadasyndromeararecasereportandliteraturereview AT chengling cronkhitecanadasyndromeararecasereportandliteraturereview AT zoukaifang cronkhitecanadasyndromeararecasereportandliteraturereview AT zhuliangru cronkhitecanadasyndromeararecasereportandliteraturereview |