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손정문(J M Sohn),박재갑(J G Park),오승근(S K Oh),박용현(Y H Park),최국진(K J Choe),김수태(S T Kim) 대한소화기학회 1982 대한소화기학회지 Vol.14 No.2
N/A Authors reviewed 8 cases of non-traurnatic hemobilia from Oct. 1st 1975 to Sep. 30th 1982, at the Department of Surgery, Seoul National University Hospital and arrived at the following conclusions. 1)Hemobilia associated with hepatobiliary malignancy were 5 cases, and hemobilia associated with hepatobiliary inflammation were 3 cases. 2) The main symptom of hemobilia associated with hepatobiliary malignancy was mostly jaundice, but those associated with hepatobiliary inflammation was gastrointeatinal bleeding. 3) 0ccult blood in feces proved very important in diagnosing hemobilia associated with hepatobiliary maligncies. 4) Blood clots in the common bile duct in patients with malignancies were helpful in confirming the diagnosis of original disease. 5) In cases of obstructive jaundice associated with hepatobiliary malignanies hemobilia must be considered in diagnosis 6) In cases of massive gastrointestinal bleeding of unknown origin, hemobilia must be considered in diagnosis, especially when the patient has a history of biliary colic, and also the exploration of the hepatobiliary area is mandatory during surgery 7) The possibility of blood clots due to minor bemobilia must be considered in differential diagnosis of filling defects in postoperative cholongiograms and unnecesary surgery must be avoided. 8) Ligation of hepatic artery branch was effective in treating symptomatic non-trarmatic hemobilia.
한국인 가족성 용종증 환자의 가계도 분석 - 한국 용종증 등록소 -
박규주 ( Kyu Joo Park ),박재갑 ( Jae Gahb Park ),최규완 ( Kyoo Wan Choi ),원치규 ( Chi Kyooh Won ),김광연 ( Kwang Yun Kim ),김세민 ( Sea Min Kim ),김영진 ( Young Jin Kim ),김용일 ( Yong Il Kim ),김응국 ( Eung Kook Kim ),김종훈 ( J 대한소화기학회 1992 대한소화기학회지 Vol.24 No.5
Familial adenomatous polyposis (FAP) is a disease characterzed by the development of 100 to several thousand colorectal adenomas, of which one or more will degenerate into carcinoma unless prophylactic colectomy is performed. It is characterized by autosomal dominant mode of inheritance, but sporadic cases without family history of the disease has been reported in up to one-third of patients. (continue...)