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임화중(Hwa Joong Yim),백근욱(Keum Wook Baek),윤석부(Seok Bu Woon),장웅기(Woong Ki Chang),김동준(Dong Jun Kim),김홍기(Hong Ki Kim),채승완(Seung Wan Chae),박영의(Young Euy Park) 대한소화기학회 1994 대한소화기학회지 Vol.26 No.2
The Peutz-Jeghers syndrome is an autosornal dominant hereditary disease characterized by hamartous polyps of the gastrointestinal tract and by mucocutaneous melanin deposits. This syndrome is clinically important because of the complications caused by gastrointestinal pol- yps and of an increased risk for the development of cancer. W e experienced a case of develop- ing an adenocarcinoma of the stomach in patient with Peutz-Jeghers syndrome, who had mucocutaneous pigmentations and gastric, small intestinal and large intestinal polyps for seven years. (Korean J Gastroentero11994; 26: 337-342)
박희봉,김동준,장웅기,임화중,백근욱 대한소화기내시경학회 1993 Clinical Endoscopy Vol.13 No.4
Gastric tuberculosis is a rare disease and the diagnoeis of gastric tuberculosis is based on either positive histological or bacteriological study. We experienced a case of gastric tuberculosis with pleural effuaion in 59 year-old woman, diagnosed by the histological study of the endoscopic biopsy specimen. Follow up endoscopic finding revealed marked improvement of gastric lesion after anti-tubercadoua medication. We reported the case with review of literature.
박희봉,최영희,이상조,박성우,임성희,문승환,임화중,박영의,이민철 대한내분비학회 1991 Endocrinology and metabolism Vol.6 No.4
The ACTH-independent forms of endogenous Cushing's syndrome are adrenal in origin. They include adrenal carcinoma, adrenal adenoma and the rare adrenal nodular hyperplasia. We report a case of Cushing's syndrome caused by ACTH-independent bilateral macronodular adrenal hyper-plasia. A 31-year-old man presented with Cushingoid feature, diabetes mellitus and hypertension. Urinaryh free cortisol and 17-hydroxycorticosteroid excretion were 637.7 g/ㅇ묘 뭉 13.2mg/day, respectively. Both were not suppressed after administration of high-dose dexamethasone. Plasma ACTH was below 10 pg/ml. In abdomen C-T, both adrenal glands were markedly enlarged and nodular in appearance. Pituitary MRI showed no abnormal finding. Bilateral total adrenal glands were enlarged, with a total weight of 240 gm, and contained multiple nodules (diameter, 0.3~5cm). Histologic examination revealed round to ovoid nodules composed of clear cells and eosinophilic granular cells. No lipofuscin-containing cells were seen and the area between nodulwas atrophic and contained small cells. (J Kor Soc Endocrinol 6:362~366, 1991)
박충기,정기석,김호중,백근욱,현인규,이명구,임화중,강성하 대한내과학회 1995 대한내과학회지 Vol.49 No.3
Empyema may be caused by many organisms and may rarely be caused by fungi, particularly in immunocompromised hosts. Acremonium species have been reported to cause superficial infection but invasive pulmonary infection was very rare and only one case has been reported in a boy with chronic granulomatous disease. We report a case of Acremonium species-related empyema thoracis and pulmonary infection in a 66-year-old man with alcoholic liver disease.