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스테로이드 치료없이 금식과 비경구 영양법으로 회복된 호산구성 복막염 및 위장염
장환준(Hwan Joon Chang),신언수(Eun Soo Shin),박혜영(Hye Young Park),한인수(In Soo Han),정숙향(Sook-Hyang Jung) 대한소화기학회 1994 대한소화기학회지 Vol.26 No.6
Eosinophilic gastroenteritis is a rare disease characterized by eosinophilic infiltration of vari- ous areas of gastrointestinal tract with gastrointestinal symptoms such as abdominal pain, vomiting, diarrhea and rarely ascites. Although its pathogenesis and natural course was not well defined,the main stay of treatment has been steroid administration with or without sur- gery. We experienced a case of diffuse eosinophilic gastroenteritis and serositis with massive ascites, which showed complete remission after conservative management such as NPO and TPN without steroid. This case suggests a speculation of pathogenesis in relation to the food allergy and self limited natural course of eosinophi)ic gastroenteritis. (Korean J Gastroente- rol 1994; 26: 1029 1033)
한인수,이홍규,박혜영,강문호,김종호,김종유,신언수,장환준,박흠례,우병완 대한내과학회 1995 대한내과학회지 Vol.48 No.1
Cavernous hemangiomas of the adrenal gland are rare, and no cases of them seem to have been reported in Korea. We report a case of adrenal hemangioma which was incidentally found in a patient with rectal cancer. The clinical presentation, rediographic characteristic, and management are also reviewed. Although rare, a hemangima should be considered in the differential diagnosis of a adrenal neoplasm.
한인수,이홍규,박혜영,강문호,김종호,김종유,신언수,장환준 대한내분비학회 1993 Endocrinology and metabolism Vol.8 No.4
Pachydermoperiostosis is a rare condition of unknown etiology, characterized by digital clubbing, periosteal new bone formatin and thickening of skin as a traid. Enlarged fingers and coarse facial features with thick, furrowed and oily skin often give fise to appearances simulating acromegaly. We describe three brothers with pachydermoperiostosis, one of whom had been misdiagnosed as having acromegaly and received hypophysectomy. The clinician should pay attention to the true diagnosis by the presence of clubbing and periosteal new bone formation and the lack of growth hormone excess despite the diagnostic pitafall dud to the gross features mimicking acromegaly. (J Kor Soc Endocrinol 8: 439~444, 1993).