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Joung Il Lee 3 Articles
A Patient with Duodenal Mucinous Adenocarcinoma Presenting as a Laterally Spreading Tumor
Myung Joon Chae, Il Hyun Baek, Yu Mi Oh, Jun Uk Lim, Jung Won Jeon, Hyun Phil Shin, Kwang Ro Joo, Joung Il Lee
Clin Endosc 2015;48(4):336-339.   Published online July 24, 2015
AbstractAbstract PDFPubReaderePub

Primary duodenal carcinoma is rare. Duodenal mucinous adenocarcinoma (DMA) is even rarer, and its associated manifestations and typical endoscopic or imaging findings are not well characterized. Herein, we report a case of primary DMA in an asymptomatic 58-year-old man who visited our hospital for a regular health screening. Upper endoscopy revealed an approximately 4-cm lesion in the second portion of the duodenum, but the mass was not visualized on computed tomography. Biopsies revealed a tubular adenoma that was subsequently resected. Frozen biopsies demonstrated DMA with a background of low-grade tubular adenoma for which we performed Roux-en-Y duodenojejunostomy and jejunojejunostomy. To our knowledge, this is the first report of a patient with DMA in Korea.


Citations to this article as recorded by  
  • Duodenal Mucinous Adenocarcinoma in a Patient With Immunodeficiency: A Case Report
    Timon Sseruwagi, Joel Musinzi, William M Mutumba, Catherine Lewis
    Cureus.2023;[Epub]     CrossRef
  • Concomitant Kinase-Dead BRAF and Oncogenic KRAS Lead to an Aggressive Biologic Behavior and Tumor Lysis Syndrome: A Case Report
    Roy Holland, Offir Ben-Ishay, Irit Ben-Aharon
    Frontiers in Oncology.2022;[Epub]     CrossRef
  • Duodenal mucinous adenocarcinoma presenting as ileus, obstructive jaundice and massive ascites: A case report
    Dongbing Ding, Yao Yao, Songbai Zhang
    Molecular and Clinical Oncology.2018;[Epub]     CrossRef
  • Calcified pancreatic and peripancreatic neoplasms: spectrum of pathologies
    Franco Verde, Elliot K. Fishman
    Abdominal Radiology.2017; 42(11): 2686.     CrossRef
  • Two Cases of Duodenal Mucinous Carcinoma
    Motoki YAMAMOTO, Makoto IWAHASHI, Hiroshi TERASAWA, Shimpei MARUOKA, Yukari TSUBOTA
    Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association).2016; 77(11): 2716.     CrossRef
  • 6,996 View
  • 71 Download
  • 4 Web of Science
  • 5 Crossref
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A Case of Biliary Cast Developed in a Patient with Long-Standing Biliary Sludge
Ja Won Koo, Na Eun Jang, Hong Joo Lee, Kwang Ro Joo, Jae Myung Cha, Hyun Phil Shin, Joung Il Lee, Sung-Jig Lim
Clin Endosc 2013;46(1):98-101.   Published online January 31, 2013
AbstractAbstract PDFPubReaderePub

Development of biliary casts is very unusual, especially in patients who have not undergone liver transplantation. Variable causes of biliary cast formation in nonliver transplantation patients have been suggested. However, stasis of bile flow and/or gallbladder hypocontractility is known to eventually result in the promotion of biliary sludge and subsequent cast formation. Here we present one case of biliary cast syndrome, which developed in a nonliver transplant patient who had biliary sludge for a long period of time, providing evidence that long-standing biliary sludge may lead to cast formation.


Citations to this article as recorded by  
  • Intensive Care Unit–Related Cholangiopathy-Induced Biliary Cast Syndrome Without Liver Transplantation: A Rare Entity
    Fnu Vikash, Sindhu Vikash, Sammy Ho, Donald Kotler, Sunny Patel
    ACG Case Reports Journal.2024; 11(2): e01269.     CrossRef
  • A Case of Biliary Cast Syndrome with Cholangiocarcinoma-like Lesion in a Patient with No History of Liver Transplantation
    Sa-Hong Jo, Ho-Cheol Choi, Sung-Eun Park, Jin-Il Moon, Jung-Ho Won, Jae-Boem Na, Yang-Won Kim, Won-Jeong Yang, Byeong-Ju Koo, Jae-Kyeong Ahn, Seong-Je Kim
    Medicina.2023; 59(7): 1272.     CrossRef
  • Biliary Cast Syndrome in an Opium Inhaler
    Reza Dabiri, Hamid Asadzadeh Aghdae, Hasan Rajabalinia, Amir Houshang Mohammad Alizadeh
    Case Reports in Gastroenterology.2013; 7(3): 376.     CrossRef
  • 6,247 View
  • 46 Download
  • 2 Web of Science
  • 3 Crossref
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Retroperitoneal Synovial Sarcoma Manifested by Obstructive Jaundice in an Elderly Woman: Case Report
Dae Ho Kim, Kwang Ro Joo, Jae Myung Cha, Hyun Phil Shin, Joung Il Lee, Jae Jun Park, Hyun Soo Kim, Dal Mo Yang
Clin Endosc 2012;45(4):428-430.   Published online November 30, 2012
AbstractAbstract PDFPubReaderePub

Synovial sarcoma is a rare type of soft tissue sarcoma that arises in tissues containing synovial fluid, usually in the extremities. It has only rare occurrence in the retroperitoneal space. Early detection of retroperitoneal synovial sarcoma is difficult, since the retroperitoneal space is highly expandable and deeply hidden. Furthermore, the presenting symptoms are often vague and nonspecific, and are related to the pressure on adjacent structures. In this study, we present an unusual case of retroperitoneal synovial sarcoma with obstructive jaundice due to intrabiliary blood clots caused by invasion of bile duct by tumor. The obstructive jaundice was relieved through endoscopic removal of the blood clots and insertion of a biliary stent.


Citations to this article as recorded by  
  • Management of primary retroperitoneal synovial sarcoma: A case report and review of literature
    Aikaterini Mastoraki, Dimitrios Schizas, Ioannis S Papanikolaou, George Bagias, Nikolaos Machairas, George Agrogiannis, Theodore Liakakos, Nikolaos Arkadopoulos
    World Journal of Gastrointestinal Surgery.2019; 11(1): 27.     CrossRef
  • Intrapelvic Retroperitoneal Synovial Sarcoma in a 15-Year-Old Adolescent Girl: A Case Report and Review of the Literature
    Stan A. Bessems, Maarten van Heinsbergen, Paul H. Nijhuis, Kees C.P. van de Ven, Frits Aarts
    Journal of Pediatric Hematology/Oncology.2019; 41(8): 627.     CrossRef
  • Primary Monophasic Synovial Sarcoma of the Liver in a 13-Year-Old Boy
    Bo Xiong, Min Chen, Feng Ye, Zhuxue Zhang, Lijuan Yin, Huifen Huang, Huijiao Chen, Hongying Zhang
    Pediatric and Developmental Pathology.2013; 16(5): 353.     CrossRef
  • 5,575 View
  • 42 Download
  • 3 Crossref
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