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Case Reports
Two Cases of Plug or Stone in Remnant Intrapancreatic Choledochal Cysts Treated with Endoscopic Retrograde Cholangiopancreatography
Eunbee Kim, Min Ho Kang, Jisun Lee, Hanlim Choi, Jae-Woon Choi, Joung-Ho Han, Seon Mee Park
Clin Endosc 2017;50(5):504-507.   Published online February 16, 2017
DOI: https://doi.org/10.5946/ce.2017.012
AbstractAbstract PDFPubReaderePub
Incomplete resection of choledochal cysts (CCs) that extend deep into the pancreas can lead to protein plug or stone formation, pancreatitis, and cholangiocarcinoma. We encountered two cases of choledocholithiasis in remnant intrapancreatic CCs (IPCCs), in which the patients exhibited symptoms after 3 and 21 years of cyst excision. A 21-year-old woman who had undergone excision of a CC, as a neonate, presented with epigastric pain. Abdominal computed tomography (CT) revealed stones inside the remnant pancreatic cyst, which were removed by endoscopic retrograde cholangiopancreatography (ERCP), and her symptoms improved. A 33-year-old woman, who underwent cyst excision 3 years ago, presented with pancreatitis. Abdominal CT showed a radiolucent plug inside the remnant pancreatic cyst. The soft, whitish plug was removed by ERCP, and the pancreatitis improved. These cases indicate that plugs and stones in CCs have the same pathogenetic mechanism, and their form depends on the time since the incomplete excision surgery.

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  • Choledochal cysts – state of the art
    Thanh Liem Nguyen, V. S. Cheremnov, Yu. A. Kozlov
    Russian Journal of Pediatric Surgery.2021; 25(1): 37.     CrossRef
  • 6,945 View
  • 130 Download
  • 1 Crossref
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Polypoid Arteriovenous Malformation Presenting with Jejunojejunal Intussusceptions in an Adult
Doo-Ho Lim, Ji Yong Ahn, Myeongsook Seo, Ji Hyun Yun, Tae Hyung Kim, Hwoon-Yong Jung, Jin-Ho Kim, Young Soo Park
Clin Endosc 2014;47(6):575-578.   Published online November 30, 2014
DOI: https://doi.org/10.5946/ce.2014.47.6.575
AbstractAbstract PDFPubReaderePub

Jejunal polypoid arteriovenous malformations (AVMs) and jejunojejunal intussusceptions are both rare. Here, we present the case of a 61-year-old woman who suffered intermittent episodes of abdominal pain over the course of 13 years. A computed tomography scan of her abdomen and pelvis revealed a distal jejunojejunal intussusception. A suspected low density mass was observed at the tip of the intussusception. Treatment comprised laparoscopic small bowel resection with end-to-end jejunostomy. The final diagnosis was a polypoid AVM measuring 5×3.5×3 cm. We suggest that polypoid AVM should be considered as a differential diagnosis in patients presenting with small intestinal neoplasms.

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  • Arteriovenous malformation that caused prolapse of the colon and was treated surgically in an infant: a case report
    Miori Kido, Kiyokuni Nakamura, Tsuyoshi Kuwahara, Yoshitomo Yasui, Hideaki Okajima, Nozomu Kurose, Miyuki Kohno
    Surgical Case Reports.2020;[Epub]     CrossRef
  • Colonic Polypoid Arteriovenous Malformation Causing Symptomatic Anemia
    Allison Rzepczynski, Jason Kramer, Shriram Jakate, Lin Cheng, Ajaypal Singh
    ACG Case Reports Journal.2019; 6(10): e00241.     CrossRef
  • Arteriovenous malformation in the sigmoid colon of a patient with Cowden disease treated with laparoscopy: a case report
    Koichi Inukai, Nobuhiro Takashima, Shiro Fujihata, Hirotaka Miyai, Minoru Yamamoto, Kenji Kobayashi, Moritsugu Tanaka, Tetsushi Hayakawa
    BMC Surgery.2018;[Epub]     CrossRef
  • Unusual Giant Arteriovenous Malformation in Jejunum: A Case Report
    DongJa Kim, JaIl Goo
    Journal of the Korean Association of Pediatric Surgeons.2017; 23(2): 52.     CrossRef
  • 5,481 View
  • 67 Download
  • 4 Web of Science
  • 4 Crossref
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Helicobacter pylori 양성인 만성 반복성 복통 환아에 대한 제균 요법의 효과
Korean J Gastrointest Endosc 2003;27(5):386-386.   Published online November 20, 2003
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  • 1 Download
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54세 남자, 수양성 설사와 구토
Korean J Gastrointest Endosc 2000;20(5):347-348.   Published online November 30, 1999
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  • 9 Download
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증례 : 식도 위장관 ; 만성복통을 주증상으로 한 면역기능이 정상인 소아에서 발생한 식도 캔디다증 1예 ( Case Reports : Esophagus , Stomach & Intestine ; A Case of Esophageal Candidiasis Presenting Recurrent Abdominal Pain in an Immunocompetent Child )
Korean J Gastrointest Endosc 1997;17(1):55-58.   Published online November 30, 1996
AbstractAbstract PDF
Candida albicans is the most common cause of infectious esophagitis and usually is an opportunistic infection in immunocompromised patients. Dysphagia and odynophagia are the usual presenting complaints and, importantly, oral lesions are absent in 50 percent of patients. The role of gastrointestinal endoscopy in diagnosing fungal infections of the esophagus is primary. It is the most definitive and often the only method of detecting esophageal candidiasis. Accurate endoscopic diagnosis by biopsy or brushing leads to the initiation nf effective therapy. We have experienced a case of esophageal candidiasis in an 11-year-old girl who was immunologically normal and whose main symptoms were epigastric abdominal pain and nausea for 4 months. The endoscopic and pathologic findings of esophageal candidiasis were presented. (Korean J Gastrointest Endosc 17: 55-58, 1997)
  • 1,330 View
  • 1 Download
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