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조민구(Min Koo Cho),김영중(Young Jung Kim),김진욱(Jin Wook Kim),서대원(Dae Won Seo),김홍남(Hong Nam Kim),장태종(Tae Jong Jang),반금진(Geum Jin Ban),김윤권(Youn Gwon Kim) 대한소화기학회 1997 대한소화기학회지 Vol.30 No.1
Since Rokitansky described the hamartoma of the spleen first in 1861, it has been a rare benign tumor composed of abnonnal rnixtures of normal splenic elements. Clinically it is asymptomatic in most patients but left upper quadrant mass, abnormal hetnatologic findings, frequent infection, fever, generalized weakness, and loss of appetite may be present in some cases. Although it can be diagnosed by roentgenologic examinations and aspiration biopsy, no one has been certain preoperatively. A case of splenic hamartoma in 35 years old male diagnosed postoperatively is presented. (Korean J Gastroenterol 1997;30:131 - 135)
종양양 위 전정부 폐쇄를 동반한 미만성 호산구성 위장관염 1 예
윤수진,노영호,조민구,김소연,이권전,반금진,한신,시석 대한소화기학회 1999 대한소화기학회지 Vol.33 No.5
Eosinophilic gastroenteritis is a rare disease characterized by tissue eosinophilia that can involve different layers of the gut wall. The pathogenesis and pathophysiology of this condition are poorly understood. Its clinical feature depends on the type of layer and location involved. The endoscopic and radiologic findings of eosinophilic gastroenteritis mimicked many other gastrointestinal diseases. We experienced a case of diffuse eosinophilic gastroenteritis in a 21-year-old male who presented severe vomiting and weight loss. After performing gastrofiberoscopy, barium study for upper gastro intestinal tract and abdominal computed tomography, we concluded that the lesion was gastric tumo with severe antral obstruction. Then, we carried out subtotal gastrectomy. We could confirm the diagnosis of eosinophilic gastroenteritis by full-thickness biopsy of the stomach wall. We report this case with a brief review of the literatures.