1.Intraabdominal tuberculosis found by abnormal finding of ampulla of Vater.
Sang Woo LIM ; Tae Dong KIM ; Tae Il LEE ; Suk KIM
Korean Journal of Medicine 2006;70(4):467-468
No abstract available.
Ampulla of Vater*
;
Duodenum
;
Tuberculosis*
2.Primary outcomes of ampullary resection, bile ductoplasty and pancreatic ductoplasty through incision of D2 duodenum
Journal of Practical Medicine 2005;510(4):35-37
Study on 4 cases of malignant tumor of Vater’s ampulla operated at Viet-Duc Hospital and 1 case treated at University of Medicine and Pharmacy at Ho Chi Minh City between August 2003 and December 2004. Results: clinical sign is biliary obstruction jaundice. Gastroduodenoscopy with flexible tube found that papilla of Vater with the diameter lower than 3cm (histological finding: carcinomas), without metastasis to adjacent duodenum. Tumor invasion into head of pancreas and the lower of choledochous duct was determined by pancreatic and liver ultrasound, CT scanner or MRI examinations, in combination with intraoperative balance, immediate biopsy of lymph nodes in group 14 and group 8, sections of bile duct, pancreatic duct and duodenum in order to ensure the elimination of surgery. Initial outcomes showed that there wasn’t post-operative complication or death.
Ampulla of Vater
;
Duodenum
;
Therapeutics
;
Surgery
3.Problems of Pathologic T Staging in Ampullary Neoplasm.
Korean Journal of Pancreas and Biliary Tract 2014;19(3):117-120
Ampulla of Vater (AoV) is a small dilated duct less than 1.5 cm long, formed by the union of pancreatic duct and common bile duct. AoV has also anatomic layer of mucosa, sphincter of Oddi, perisphincteric or duodenal submucosa, and duodenal proper muscle, which corresponds to mucosa, muscularis mucosa, submucosa, and proper muscle layer of other gastrointestinal tract organs, respectively. Because of its small compact size and variation of anatomic structure, it is sometimes difficult to identify layering architecture of AoV. This anatomic difficulty may cause some problem in T classification of ampullary carcinoma (AC). The most confusing point in T classification is the vague definition of T2, "Tumor invades duodenal wall". It seems that duodenal wall includes duodenal mucosa, submucosa, and proper muscle layer. However there is no precise description or definition about duodenal wall that might lead personal variation in T classification of AC staging. We found that clinical course of AC with perisphincteric and/or duodenal submucosal invasion is more close to AC with T2 than T1. Although it is described as T1b according to T classification scheme of ordinary gastrointestinal tract cancer, we thought AC with T1b may have more high-grade malignant potential than those of other gastrointestinal (GI) tract malignancy. AC showed various clinicopatholgic findings that represent heterogeneous tumor groups within category of AC. Recently site-specific classification of AC was introduced, and it showed relatively well-categorized clinical prognosis. It may be reasonable to understand site-specific tumorigenesis in AC. The standard gross protocol is needed to evaluate pathologic T classification of AC. In conclusion, ampullary neoplasm is composed of various subtypes, which require a separate approach according to anatomic epicenter of ampullary neoplasm. Although submucosal invasion in AC was classified into pT1b, its' biologic behavior is more close to pT2.
Ampulla of Vater
;
Carcinogenesis
;
Classification
;
Common Bile Duct
;
Duodenum
;
Gastrointestinal Neoplasms
;
Gastrointestinal Tract
;
Humans
;
Mucous Membrane
;
Neoplasm Staging
;
Pancreatic Ducts
;
Prognosis
;
Sphincter of Oddi
4.Percutaneous transhepatic removal of common bile duct stone: a case report.
Yong Moon SHIN ; Joon Koo HAN ; Byung Ihn CHOI ; Jae Hyung PARK ; Man Chung HAN ; Yong Hyun PARK
Journal of the Korean Radiological Society 1992;28(1):24-27
Percutaneous transhepatic intervention for removal of common bile duct stones is introduced as a secondary choice of treatment in the high-risk patient. Through a percutaneous transhepatic biliary drainage catheter, a Dormia basket was inserted and the stone was entraped. Then the stone was crushed and fragments were passed spontaneously to the duodenum through the Ampulla of Vater. We experienced one case of successful treatment of a common bile duct stone using percutaneous transhepatic insertion of the Dormia basket.
Ampulla of Vater
;
Catheters
;
Common Bile Duct*
;
Drainage
;
Duodenum
;
Humans
5.A clinical analysis of primary malignant tumors of duodenum.
Wan Suk PARK ; Sun Whe KIM ; Kuhn Uk LEE ; Yong Hyun PARK ; Kuk Jin CHOE ; Jin Pok KIM
Journal of the Korean Surgical Society 1992;43(2):211-219
No abstract available.
Duodenum*
6.A Case of Endoscopic Management of Dieulafoy's Lesion in the Ampulla of Vater.
Ki Won HWANG ; Jae Hyung LEE ; Joo Ho LEE ; Sang Yong LEE ; Tae Oh KIM ; Gwang Ha KIM ; Jeong HEO ; Dae Hwan KANG ; Geun Am SONG ; Mong CHO
Korean Journal of Gastrointestinal Endoscopy 2006;32(5):357-360
Dieulafoy's lesion is an uncommon but important cause of massive upper gastrointestinal bleeding. The lesion usually occurs in the lesser curvature of the stomach within 6 cm of the gastroesophageal junction but extragastric locations of Dieulafoy's lesion are rare. In this study, diagnosis of Dieulafoy's lesion was frequently made by endoscopy instead of surgery. Hemostasis was achieved by endoscopic treatment in more than 90% of patients. We report the successful application of endoscopic hemoclipping for treatment of active bleeding from Dieulafoy's lesion in the ampulla of Vater of the duodenum.
Ampulla of Vater*
;
Diagnosis
;
Duodenum
;
Endoscopy
;
Esophagogastric Junction
;
Hemorrhage
;
Hemostasis
;
Humans
;
Stomach
7.Congenital Duodenal Web in a Young Adult.
Hwan Hyo LEE ; Hyung Guk KIM ; Young Yuk YOON
Journal of the Korean Surgical Society 2003;64(4):343-347
Congenital duodenal web in adult life is an extremely rare condition, which results from an incomplete recanalization of the duodenum during early embryologic development. We report a case of congenital duodenal web in a 23-year-old man who complained of postprandial epigastric pain and fullness, as well as nausea since childhood. The plain abdomen showed a double-bubble sign. The UGI study showed a marked dilatation of the proximal duodenum and a delayed passage of barium into the third portion of the duodenum. Abdominal ultrasonography and CT revealed a marked dilatation of the proximal duodenum and a duodenal web with windsock deformity, which originated from the ampulla of Vater and extended to the third portion of the duodenum. A winsock web with a 0.9 cm eccentric aperture and a healed ulcer proximal to the ampulla of Vater were observed during a longitudinal duodenotomy. The web was excised circumferentially and the duodenum was closed transversely in a Heineke-Mikulicz fashion.
Abdomen
;
Adult
;
Ampulla of Vater
;
Barium
;
Congenital Abnormalities
;
Dilatation
;
Duodenum
;
Humans
;
Nausea
;
Ulcer
;
Ultrasonography
;
Young Adult*
8.A Case of Lymphatic Metastasis to Ampulla of Vater from Gastric Adenocarcinoma.
Jin Bum KIM ; Bai Young KIM ; Moo Yous CHOO ; Gyo Seung HWANG ; Nam Hun KIM ; Jae Young KWAK ; Myoung Kee LEE ; Youn Hui CHO ; Young Lock LEE ; Kyu Sik KIM ; Young Ho KIM ; Joo Taik LEE ; Kyung Ho KIM
Korean Journal of Medicine 1997;53(4):591-595
Cancer of the stomach is responsible for approximately 650,000 deaths globally each year and is probably second only to lung cancer worldwide as an overall cause of cancer-related mortality. Similar to the situation with most adenocarcinomas of the gastointestinal tract, carcinomas of the stomach can spread by local extension to adjacent normal structures and can develop lymphatic, peritoneal, and distant metastases. The tumor cells, can also permeate diffusely into the lymphatic plexus of the bowel, more often at the level of the upper duodenum hut sometimes down into the distal ileum and the large bowel. We report a case of lymphatic metastasis of gastric adenocarcinoma to the ampulla of Vater with review of the literature.
Adenocarcinoma*
;
Ampulla of Vater*
;
Duodenum
;
Ileum
;
Lung Neoplasms
;
Lymphatic Metastasis*
;
Mortality
;
Neoplasm Metastasis
;
Stomach
;
Stomach Neoplasms
9.Ngiodysplasia in Gaint Diverticulum of Transverse Duodenum Causing Massive Gastrointestinal Bleeding: A Case Report.
Pil Yeob CHOI ; Sang Wook LEE ; Jae Soo KWON ; Young Soon SUNG ; Myoung Ho RHO ; Oh Joon HWON
Journal of the Korean Radiological Society 1998;39(6):1185-1187
The incidence of duodenal diverticulum found incidentally during upper gastrointestinal roentgenographicexamination varies between 2% and 5%. The majority of cases occur along the medial aspect of the second portion of the duodenum, within 2.5cm of the ampulla of Vater. The majority of duodenal diverticula are asymptomatic, but insome cases, complications such as diverticulitis, hemorrhage, perforation, and fistula formation occur in thethird and fourth portions of the duodenum. We describe a case of giant diverticulum of the transverse duodenum,revealed by UGI and angiography, massive gastrointestinal bleeding in a 80-year-old patient.
Aged, 80 and over
;
Ampulla of Vater
;
Angiography
;
Diverticulitis
;
Diverticulum*
;
Duodenum*
;
Fistula
;
Hemorrhage*
;
Humans
;
Incidence
10.A Case of Tubulovillous Adenoma Involving Ampulla of Vater, which Recurred after Local Excision.
Kang Hyeon CHOE ; Sung Koo LEE ; Myung Hwan KIM ; Young Il MIN ; Suck Joon HONG
Korean Journal of Gastrointestinal Endoscopy 1991;11(1):93-96
The villous adenoma of the duodenum is a rare disease and a considerable portion of the cases are known to be associated with malignancy. Although the diagnosis can be made with duodenoscopy, some cases showed false negative rate for malignancy detection with endoscopic biopsy only. So Whipple's operation is preferred than local excision. We experienced a case of tubulovillous adenoma involving ampulla of Vater, which recurred after local excision. So we report a case of tubulovillous adenoma involving ampulla of Vater with relevant literature.
Adenoma*
;
Adenoma, Villous
;
Ampulla of Vater*
;
Biopsy
;
Diagnosis
;
Duodenoscopy
;
Duodenum
;
Rare Diseases