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Hyeung Cheol Moon 2 Articles
A Case of Endoscopic Removal of a Giant Appendicolith Combined with Stump Appendicitis
Du Jin Kim, Sang Wook Park, Seung Ho Choi, Jong Hoon Lee, Kyoung Wan You, Geum Soo Lee, Hyeung Cheol Moon, Gun Young Hong
Clin Endosc 2014;47(1):112-114.   Published online January 24, 2014
DOI: https://doi.org/10.5946/ce.2014.47.1.112
AbstractAbstract PDFPubReaderePub

Stump appendicitis is an acute inflammation of the residual appendix and is a rare complication after appendectomy. The physician should be aware of the possibility of stump appendicitis in patients with right lower abdominal pain after appendectomy so that delayed diagnosis and treatment can be prevented. Stump appendicitis is usually treated by surgical resection, and endoscopic treatment has not been reported previously. A 48-year-old man who had undergone appendectomy 35 years earlier presented to the hospital because of right lower quadrant discomfort. A computed tomography scan showed a large stone in the residual appendix. Colonoscopic findings revealed a large, smooth, protruding lesion at the cecum with a stone inside the appendiceal orifice. Endoscopic removal after incision of the appendiceal orifice was performed successfully.

Citations

Citations to this article as recorded by  
  • SpyGlass/Cholangioscope-Assisted Colonoscopic Removal of Appendicolith as a Nonsurgical Alternative for Stump Appendicitis Management
    Aarushi Sudan, Dhawani Julka, Sunny A. Patel
    ACG Case Reports Journal.2024; 11(7): e01430.     CrossRef
  • Routine colonoscopy with a surprise in the cecum: It’s a giant appendicolith! A Case report and review of the literature
    Magnus Kock am Brink, Christa Schmidt, Thies Daniels, Guntram Lock
    Zeitschrift für Gastroenterologie.2024;[Epub]     CrossRef
  • Stump appendicitis – a systematic analysis
    Sajad Ahmad Salati
    Polish Journal of Surgery.2021; 94(1): 1.     CrossRef
  • Giant Appendicolith: A Case Report and Review of the Literature
    Robert A Pahissa, Kevin M Lin-Hurtubise
    Military Medicine.2020; 185(9-10): e1851.     CrossRef
  • Colonoscopic removal of a giant appendiceal faecolith without appendectomy for acute appendicitis – a video vignette
    Chao‐Wen Hsu
    Colorectal Disease.2018; 20(11): 1056.     CrossRef
  • Giant Appendicolith in Acute Exacerbation of Chronic Appendicitis: Case Report and Literature Review
    Alberto Manuel González Chávez, Ricardo Ray Huacuja Blanco, Mario Andrés González Chávez, Silviano Ríos Pascual, Diego Abelardo Álvarez Hernández, José de Jesús Curiel Valdés
    Surgical Science.2017; 08(11): 457.     CrossRef
  • Asymptomatic giant appendicolith managed conservatively
    Darren Leonard Scroggie, Maitham Al-Whouhayb
    Journal of Surgical Case Reports.2015; 2015(11): rjv149.     CrossRef
  • 9,560 View
  • 74 Download
  • 8 Web of Science
  • 7 Crossref
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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  
  • 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
  • 8,325 View
  • 78 Download
  • 4 Crossref
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