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조성락(Sung Rag Cho),김주호(Ju Ho Kim),한규호(Kyu Ho Han),박인철(In Cheol Park),김순관(Soon Kwan Kim),양만석(Man Seok Yang),허갑도(Gap Do Hur),최환주(Hwan Joo Choi),지정희(Jung Hee Ji) 대한소화기학회 1989 대한소화기학회지 Vol.21 No.3
This paper describes a unique case of concurrent malignant lymphoma of the colon and small intestine. Primary gastrointestinal lymphoma primarily confined to gastrointestinal tract is relatively rare disease, and the concurrent lymphoma of colon and small bowel is very rare in reported cases. We experienced of malignant lymphoma of entire ileum and colon, especially cecum. Ileum was widely involved, and colonic lumen was stricture and mucosal fold was destructed by polypoid mass and ulceration. He was expired due to ileal perforation. We report this case with a review of the literature.
조성락(Sung Rag Cho),나산균(San Gyun Rha),문성수(Seong Soo Moon),한규호(Kyu Ho Han),박인철(In Cheol Park),김순관(Soon Kwan Kim),양만석(Man Seok Yang),허갑도(Gap Do Hur),최태룡(Tae Lyong Choi) 대한소화기학회 1991 대한소화기학회지 Vol.23 No.1
Unilobular atrophy or hypoplasia involving the hepatic lobes is not uncommon on the left side. It is distinctly uncommon on the right, where it probably represents an developmental anomaly if no other etiological factor is demonstrable. So we report a case of hypoplasia of right hepatic lobe.
이상인(Sang In Lee),최세식(Se Seek Chol),배무현(Mu Hyun Bae),김종훈(Jong Hoon Kim),최익수(Ik Su Choi),김천환(Chun Whan Kim),구호성(Ho Sung Goo),이민기(Min Ki Lee),나산균(San Gyun Rha),허갑도(Gap Do Hur) 대한소화기학회 1995 대한소화기학회지 Vol.27 No.2
Primary malignant melanoma of esophagus is rare and its symptoms are similar to those of squamous cell carcinoma. In general, this tumor tends to be polypoid with smooth intact overlying mucosa or be pediculated and irregular. Microscopically, characteristic features are junctional lenti- ginous growth pattern and tendency to expand and fill the submucosa without invading the muscularis. Primary malignant melanoma should be radiologically differentiated with unusual esophageal tumor, particularly if the lesion is polypoid. Because of the patentially widespread intramural component, surgical treatment requires a radical procedures with a far greater margin than for the usual squamous cell carcinoma. Despite these measures, however the prognosis is poor, with a 5 year survival of 4.2%. It is usually fatal within one year. The case of a 64-year-old man with esophageal malignant melanoma is described, and review of the llterature in presented related studies. (Korean J Gastroenterol 1995;27:245 - 250)
이상인,문성수,허갑도,나산균,조성락,김순관,최태룡,변상준,최세식 대한내과학회 1992 대한내과학회지 Vol.43 No.1
Choledochal cyst is a rare congenital malformation of the pancreaticobiliary system. Cystic dilatation of the biliary tree has been reported in many forms. The etiology is multifaceted and evidence of the existence of both acquired and congenital cyst is presented. The anomalous pancreaticobiliary ductal union (APBD) has received attention because of its importance in pathogenesis of the pancreaticobiliary disease. APBD is associated with congenital cystic dilatation of common bile duct and carcinoma of gall bladder. We report two cases of choledochal cyst combined with anomalous pancreaticobiliary ductal union.
Ulcerative Colitis 를 동반한 Lunch Syndrome 1 1 예
김홍식,김상준,김주호,허갑도,최덕례,조성락 대한내과학회 1988 대한내과학회지 Vol.35 No.2
Lynch syndrome I is primarily caused by inherited factors and patients are susceptible to colonic cancer on a family basis. Virtually all family members who have inherited the critical gene can be expected to develop cancer eventually. It is therefore extremely important that biomarkers be investigated which might enable genotype carrier identification before phenotypic expression(clinical cancer). This syndrome appears to be inherited in autosomal dominant fashion with high penetration and is characterized by a lack of antacedent. Much of colonic cancer in young adults predeliction for occurance in the proximal colon and is associated with multiple primary colonic cancer, both synchronous and metachronous.
김홍식,김상준,김주호,허갑도,최덕례,조성락,지정희 대한내과학회 1987 대한내과학회지 Vol.33 No.3
Primary atrophy and lipomatosis of the pancreas in adults presenting with pancreatogenous steatorrhea and/or diabetes mellitus is an unusual pancreatic disease. This condition is characterized pathologically by almost complete disappearance of the acinar cells and by disappearance of the islets of Langerhans to a lesser extent, and fatty infiltration. No specific causative factors have been demonstrated. As we understand that none of the case reported in Korea up to date concerning the primary atrophy of pancreas associated with lipomatosis, authors report a case of total fat replacement of the exocrine pancreas with atrophy of acinar cells accompany with DM diagnosed by ERCP and surgical exploration.
김상준,박인철,김주호,한규호,김덕규,허갑도 대한내분비학회 1988 Endocrinology and metabolism Vol.3 No.1
Periodic paralysis is a group of diseases of unknown cause characterized byrecurrent attacks of weakness or paralysis of the limb muscles, accompanied byloss of deep reflex and failure of the muscles to respond to electrical stimulation. We have experienced a case of periodic paralysis in a 42 years old male who had frequent attacks of flaccid paralysis of the trunk and limb muscles. The diagnosis was easily established by clinical features and electromyographic findings. We found that his plasma renin activity was high during and after attack. But its significance in periodic paralysis was unclear.