• 제목/요약/키워드: Choledochal Cyst

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Perforated Choledochal Cyst: Its Clinical Implications in Pediatric Patient

  • Kim, Soo-Hong;Cho, Yong-Hoon;Kim, Hae-Young
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제23권3호
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    • pp.259-265
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    • 2020
  • Purpose: Perforation of choledochal cyst (CC) is a relatively rare clinical presentation in pediatric populations and difficult to predict preoperatively. We assess the clinical implications by comparing clinical parameters based on a single-center experience between perforated and nonperforated CC to facilitate the appropriate management for future interventions. Methods: A total of 92 cases of CC in pediatric patients (aged <18 years) who received surgical management between January 2003 and December 2018 at a Pusan National University Children's Hospital were reviewed. After screening the clinical features of perforated cases, we compared the demographic findings, clinical characteristics, and some laboratory results between the perforated and nonperforated groups. Results: Perforated CC was identified in 8 patients (8.7%), and nonperforated CC in 84 patients (91.3%). Perforation can be classified into three categories: free perforation of cyst (3 cases), pinpoint perforation of cyst (2 cases), and necrotic change of cyst (3 cases). CC perforation occurred significantly more commonly in patients aged <24 months. Clinically, the perforated group showed significantly higher frequency of fever and higher C-reactive protein (CRP) level during the initial visit. Conclusion: Perforation is more likely to be suspected in patients aged <24 months presenting together with fever and high CRP level in the initial visit. It is also necessary to keep in mind that it indicates not only a possibility of complicated disease status regardless of its association with stones but also a difficulty of applying a minimal invasive procedure and relatively increased length of hospital stay.

췌담관 합류이상의 실험동물 모델 (An Experimental Animal Model of Anomalous Pancreaticobiliary Duct Union)

  • 한석주;장항석;김종성;한진수;김호근;황의호
    • Advances in pediatric surgery
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    • 제4권2호
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    • pp.100-109
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    • 1998
  • The anomalous pancreaticobiliary duct union (APBDU) might cause the formation of choledochal cyst and malignancies of hepatopancreaticobiliary system. The purpose of this study is to make an experimental animal model of APBDU similar to that of human. One to two-month-old Mongrel dogs (n=12) were divided into two groups; the control group (n=2) had a sham operation performed, and in the experimental group (n=10) the end of distal ' common bile duct (CBD) was anastomosed to the side of the dorsal pancreatic duct making APBDD. Serum was obtained for chemical analysis on the 10th postoperative day. The dogs were sacrificed at the 5th week (n=3), the 6th week (n=3), the 7th week (n=2), the 8th week (n=2) and the 6th month (n=2) after the experimental surgery. With sacrifice, operative cholangiogram was taken, and bile juice was obtained for chemistry and bacterial culture. The en-bloc specimens of the hepatopancreaticobiliary system were removed for microscopic examination. Serum and bile juice amylase levels were elevated in the experimental group(n=10), but not in the control group(n=2). Operative cholangiograms of control group revealed no evidence of bile duct dilatation.. On the other hand, the bile duct in the experimental group was markedly dilated without any evidence of stenosis at the anastomosis site (n=10). Histologic examination of the hepatopancreaticobiliary system in the experimental group resembled the findings of choledochal cyst in human. The APBDU of this animal model can produce bile duct dilatation by pancreaticobiliary reflux. We think that this animal model can be potentially promising for the research about the APBDU associated hepatopancreaticobiliary diseases.

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담관낭종 -대한소아외과학회회원 대상 전국조사- (Choledochal Cyst in Korea - A Survey by the Korean Association of Pediatric Surgeons -)

  • 최금자;김대연;김상윤;김성철;김신곤;김우기;김인구;김재억;김재천;김해영;김홍주;박귀원;박우현;박진영;백홍규;서정민;송영택;오수명;유수영;이두선;이명덕;이석구;이성철;박영식;이태훈;정상영
    • Advances in pediatric surgery
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    • 제9권1호
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    • pp.45-51
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    • 2003
  • 본 조사 결과는 32개 병원의 39명의 회원에 의해 수술받은 환자 348명의 기록과 회원 37명의 설문 응답자를 분석한 것으로 많은 수의 기록지가 내용이 불충분하거나 일치되지 않은 기술로 인해 자료로서의 한계가 있었다. 특히 췌담관합류 이상에 대한 기록 중 약 절반이 미상으로 기록된 것에서 알 수 있드시 자료가 매우 미흡하였고, 담관낭종의 유형을 정하는 것 예후 인자 및 산 전 진단된 담관낭종의 수술 적기등에 대하여도 회원마다 견해 차이가 있으나 심도있는 토론이 이루어지지 않았다. 따라서 이 결과를 외국의 통계 분석과 비교하는 것 보다는 회원들의 향 후 진료와 연구에 참고가 될 수 있다는 것에 의미를 두고자 하며, 회원들이 동일한 등록지를 작성하는 전향적 연구로 우리나라 담관낭종에 대한 분류, 췌담관 합류이상, 예후 인자들에 대한 재 논의의 출발점이 되기를 기대한다.

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소아에서 담췌관 질환에 대한 자기공명 담췌관조영술의 진단적 유용성 (The Usefulness of MRCP in the Evaluation of Pancreaticobiliary Diseases in Children)

  • 엄지현;이승연;정기섭
    • Clinical and Experimental Pediatrics
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    • 제45권11호
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    • pp.1381-1388
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    • 2002
  • 목 적: MRCP는 간담도췌장 질환을 진단하는데 있어서 비침습적인 방법으로 매우 유용한 것으로 알려져 있다. 본 연구의 목적은 간담도췌장 질환이 의심되는 소아에서 MRCP의 진단적 유용성에 대해 알아보고자 한다. 방 법: 1996년 10월부터 2001년 5월까지 연세의대 세브란스병원 소아과에 간담도췌장 질환으로 입원하여 복부 초음파 및 MRCP를 시행한 환아 70례를 대상으로 하였다. 환아의 최종 진단은 수술, 조직검사 소견, 임상 소견, 기타 검사 등을 토대로 하였다. 결 과 : 1) 대상 환아는 총 70례로 남녀비는 1 : 1.2였으며 평균 연령은 $2.6{\pm}3.3$세였다. 2) 간기능 검사상 혈청 AST, ALT 치는 각각 $192.7{\pm}139.6IU/L$, $182.7{\pm}143.8IU/L$이었고, 총 빌리루빈치, 직접 빌리루빈치는 각각 $6.9{\pm}3.7mg/dll$, $4.8{\pm}2.4mg/dll$이었다. 3) 간담도 췌장질환의 원인은 담도폐쇄증 25례(35.7%), 신생아 간염 18례(25.7%), 담관낭종 16례(23%)로 이 중 APBDU를 동반한 경우가 7례(10.0%), APBDU를 동반하지 않은 경우가 6례(12.9%)였으며, 전염성 단핵구증, 전격성 간염, 콕시엘라증(coxiellosis) 등으로 인한 담즙 정체성 간염이 5례(7.1%), 경화성 담도염이 2례(2.8%), 이차성 담도 경화증은 1례(1.4%), 만성 재발성 췌장염 환아가 3례(4.3%)였다. 4) 수술 소견과 병리 조직학적 소견을 기준으로 할 때 간담도췌장질환에 대한 복부 초음파의 진단의 정확도 75.7%에 비해 MRCP는 97.1%로 높았다. MRCP의 예민도와 특이도는 담도폐쇄증의 경우 각각 100%, 98%였고, APBDU가 동반된 담관낭종의 경우 87.5%, 100%였으며, APBDU가 동반되지 않은 담관낭종, 경화성 담도염, 만성 반복성췌장염은 양자 모두 100%였다. 결 론 : 본 연구에서 MRCP는 간담도췌장 질환을 진단하는데 있어서 편리하고 안전하며 비침습적인 방법으로서 그 진단율 또한 다른 검사에 비해 뛰어나 소아에서 간담도췌장질환이 의심될 때 우선적으로 시행할 수 있는 매우 유용한 검사임을 알 수 있었다.

Cyst Size in Fetuses with Biliary Cystic Malformation: An Exploration of the Etiology of Congenital Biliary Dilatation

  • Hattori, Kengo;Hamada, Yoshinori;Sato, Masahito
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제23권6호
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    • pp.531-538
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    • 2020
  • Purpose: Our aim was the longitudinal assessment of cyst size in fetuses with biliary cystic malformation (BCM) to explore its etiology and the possibility of antenatal differentiation between biliary atresia (BA) and congenital biliary dilatation (CBD). Methods: We conducted a retrospective review of all patients diagnosed antenatally with BCM from 1994 to 2014 at our institutions. Results: The study cohort comprised of three patients with BA and six with CBD. There were no significant differences in the gestational age and cyst size at the first detection of BCM between the two groups. In fetuses with CBD, the cyst size steadily increased as the gestational age advanced, while it fluctuated around 1.5 cm and remained below 2.1 cm in those with BA. However, the ratio of cystic area to fetal trunk area was approximately constant due to linear fetal growth in fetuses with CBD. Conclusion: Fetuses with BCM <2.1 cm in the late gestation period were more likely to have BA than CBD. Our observation of cyst enlargement with advancing gestational age in the CBD group was attributed solely to fetal growth. Biliary dilatation in fetuses with CBD and BA might be completed at the onset of BCM.

Spontaneous Perforation of Common Bile Duct: Abscess Formation Presenting as a Choledochal Cyst

  • Kim, Cho Hee;Kim, Dae Jung;Kim, Kyoung Ah;Choi, Sung Hoon;Kwon, Chang-Il
    • Investigative Magnetic Resonance Imaging
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    • 제20권4호
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    • pp.254-258
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    • 2016
  • Spontaneous perforation of the bile duct without any traumatic or iatrogenic injury is extremely rare. We report a case of abscess formation related to spontaneous perforation of the common bile duct by a gallstone, mimicked a cholecochal cyst.

Management of Pediatric Patients Presenting with Acute Abdomen Accompanying Dilatation of the Common Bile Duct

  • Kim, Young A;Kim, Gyung Min;Chun, Peter;Hwang, Eun Ha;Mun, Sang Wook;Lee, Yeoun Joo;Park, Jae Hong
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • 제21권3호
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    • pp.203-208
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    • 2018
  • Purpose: The aim of this study was to describe our treatment experiences with patients who had acute abdomen (AA) with common bile duct (CBD) dilatation. Methods: The treatment outcomes in children with AA and CBD dilatation were retrospectively reviewed. According to the shape of the intrahepatic bile ducts on ultrasonography (US), the origin of the pain was estimated as choledochal cyst (CC) complication or choledocholithiasis in normal CBD. Patients with complicated CC underwent surgery, and patients with choledocholithiasis in a normal appearing CBD underwent symptomatic treatment initially. Results: Of the 34 patients, 30 (88.2%) were female. The mean age of the patients was $6.4{\pm}4.9$ (range, 0.8-17) years. Seventeen (50.0%) patients had CBD stones and 17 (50.0%) did not. Surgical treatment was performed in 20 (58.8%) patients, 2 of whom underwent preoperative stone removal with endoscopic retrograde cholangiopancreatography and an operation. Conservative treatment was applied in 12 (35.3%) patients (8 with and 4 without stones), 1 of whom developed symptom relapse and underwent an operation. Among the 8 patients with CBD stones, 4 (4/17, 23.5%) had complete resolution of the stones and recovery of the CBD diameter after conservative treatment. US findings of patients with stone showed a fusiform or cylindrical shape of the CBD in 14 (82.4%) patients. Conclusion: The presence of stones in the distal CBD and the US features of CBD dilatation may be helpful to diagnose and treat the causes of biliary dilatation. Conservative treatment can be considered as initial therapy in patients with uncomplicated CBD dilatation with stone.

A Case of Double Primary Cancer (Gallbladder cancer and pancreatic cancer) in Patient with Anomalous Union of Pancreaticobiliary Duct

  • Sung Yong Han;Dong Uk Kim;Geun Am Song
    • Journal of Digestive Cancer Research
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    • 제3권1호
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    • pp.42-44
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    • 2015
  • Anomalous union of the pancreaticobiliary duct (AUPBD) has been shown to predispose to carcinomas of the biliary tract (bile duct and gallbladder) and pancreatic cancer because of chronic recurrent inflammatory reaction due to pancreatic or bile juice refluxes. However, pancreatic duct would be less affected by the bile because of the relatively higher intraductal pressure of the pancreatic duct. We report a case of metachronous pancreatic cancer in AUPBD patient without choledochal cyst who underwent cholecystectomy because of gallbladder cancer.

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원위부 총담관 결석으로 오인된 결석을 동반한 총담관류 치료 (Choledochocele containing a stone mistaken as a distal common bile duct stone)

  • 곽태영;박창환;엄석현;황홍석;정덕원;서지영;김영성;곽동협
    • Journal of Yeungnam Medical Science
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    • 제32권1호
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    • pp.60-64
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    • 2015
  • A choledochocele is an expanded sac of the duodenal side of the distal common bile duct (CBD), and is categorized as a type III choledochal cyst. Unlike other choledochal cysts, it can be easily overlooked because of its very low prevalence, non-specific clinical symptoms, and lack of distinctive radiological findings. However, a patient having a repeated pancreaticobiliary disorder with an unknown origin, frequent abdominal pain after cholecystectomy, or repeated non-specific gastrointestinal symptoms can be suspected as having a choledochocele, and a more accurate diagnosis can be achieved via endoscopic retrograde cholangiopancreatography (ERCP) and endoscopic ultrasound. Because it rarely becomes malignant, a choledochocele can be treated via endoscopic sphincterotomy (EST) and surgical treatment. The authors were able to diagnose choledochocele accompanied by a stone in a patient admitted to the authors' hospital due to cholangitis and pancreatitis. The patient's condition was suspected to have been caused by a distal CBD stone detected via multiple detector computed tomography and ERCP, and was successfully treated via EST.

신세뇨관 확장증, Caroli 증후군 및 총 담관낭을 동반한 선천성 간 섬유증 1례 (A Case of Congenital Hepatic Fibrosis Accompanied by Renal Tubular Ectasia, Caroli Syndrome and Choledochal Cyst)

  • 최봉석;배상남;임영탁;박재홍;이창훈;이준우
    • Clinical and Experimental Pediatrics
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    • 제45권7호
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    • pp.923-927
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    • 2002
  • 우연히 발견된 간비장 종대를 주소로 내원한 3세 여아에서 신낭종을 동반한 선천성 간섬유화증을 진단한 예를 경험하였기에 문헌 고찰과 함께 보고하는 바이다.