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2 "Enteritis cystica profunda"
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Case Report
A Case of Enteritis Cystica Profunda in the Ampulla of Vater Mimicking Choledochocele
Kyoung Wan You, Sang Wook Park, Geum Soo Lee, Du Jin Kim, Hyeung Cheol Moon, Gun Young Hong
Clin Endosc 2013;46(2):178-181.   Published online March 31, 2013
DOI: https://doi.org/10.5946/ce.2013.46.2.178
AbstractAbstract PDFPubReaderePub

Enteritis cystica profunda is a very rare disease in which a mucin-filled cystic space is surrounded partially with nonneoplastic columnar epithelium in the submucosa of the small intestine. Most of the cases are accompanied by intestinal diseases, and the disease usually occurs in the jejunum and the ileum and there has been no report of a case that occurred in the ampulla of Vater. A 58-year-old healthy female patient without any particular symptom visited the hospital to get additional examination for a mass found on the ampulla of Vater by accident. In esophagogastroduodenoscopy, a cystic mass showing a positive pillow sign was found on the ampulla of Vater. Endoscopic retrogradecholangiopancreatography was conducted as choledochocele was suspected, but no abnormality was found in the biliary system. In endoscopic ultrasonography, multiseptated cystic structures were detected in the submucosal layer of the duodenum. The lesion was resected completely through endoscopic snare polypectomy and the case was histologically diagnosed as enteritis cystica profunda.

Citations

Citations to this article as recorded by  
  • Bowel Obstruction Due to the Mesenteric Mass Being an Enteritis Cystica Profunda: A Case Report
    Meshael S Albahli, Fares Ali M Aljarallah, Ali K Alshaya, Nourah Alabdulaaly, Khaled Altoukhi, Haider A Alshurafa
    Cureus.2025;[Epub]     CrossRef
  • Enteritis cystica profunda: Case report and literature review
    Ricardo E. Núñez-Rocha, Felipe Girón, Mario Latiff, Carlos Eduardo Rey, Lina Rodríguez, Juan David Hernández
    International Journal of Surgery Case Reports.2023; 106: 108148.     CrossRef
  • Enteritis cystica profunda with lipoma in the second portion of the duodenum: a case report
    Beom Jin Shim, Seung Keun Park, Hee Ug Park, Tae Young Park
    Journal of Yeungnam Medical Science.2022; 39(1): 72.     CrossRef
  • Ulcerated choledochocele: A case report
    E. Ray-Offor, S.N. Elenwo, P.O. Igwe, C. Ngeribara
    International Journal of Surgery Case Reports.2016; 28: 42.     CrossRef
  • A Case of Enteritis Cystica Profunda Accompanied by a Lipoma in the Duodenal Bulb
    Dae Sung Lee, Hae Ryong Jeong, Jin Ok Kim, Hye Jin Tae, Ho Soon Choi, Hye In Ahn, Seung Sam Paik
    Korean Journal of Medicine.2014; 86(3): 314.     CrossRef
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A Case of Enteritis Cystica Profunda in the Duodenal Bulb
Hee Jong Chang, M.D., Jae Il Jung, M.D., Myung Chan Kim, M.D., Dong Hui Cho, M.D., Dong Sik Cho, M.D., Sang Hun Lee, M.D., Si Woo Kim, M.D., Sung Chul Cha, M.D., Yu Gin Cho, M.D., Yun Chul Seok, M.D., Sung Seog Ki, M.D. and Haeng Ji Kang, M.D.*
Korean J Gastrointest Endosc 2005;31(6):419-422.   Published online December 30, 2005
AbstractAbstract PDF
Enteritis cystica profunda (ECP) is characterized by mucin-filled cystic spaces that are partially lined by non-neoplastic columnar epithelium, and these are found in the wall of the small bowel. This is a very rare disease compared to cystica profunda involving the stomach or colon. The cause of ECP is still unclear. Most ECP is related to or it may accompany other intestinal diseases. We encountered one case of ECP of the duodenal bulb that presented as polyp, and this was not related to adenocarcinoma or any other intestinal diseases like Crohn's disease or ulcerative colitis. Endoscopic polypectomy was done and the ECP was later confirmed through histological evaluation. (Korean J Gastrointest Endosc 2005;31:419⁣422)
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