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이배진(Bai Jin Lee),박정영(Jung Young Park),이희영(Hi Young Lee),강효승(Hyeo Seon Kang),이종영(Jong Young Lee),변동일(Dong Il Byun),김형길(Hyung Gil Kim),이수남(Su Nam Lee) 대한소화기학회 1998 대한소화기학회지 Vol.30 No.4
Eosinophilic gastroenteritis is a rare condition of unknown cause characterized by peripheral eosino- philia, eosinophilic infiltration of the gastrointestinal tract, and gastrointestinal symptomatology. Eosinophi]ic gastroenteritis is generally classified according to the layer of gastrointestinal tract involved. Especially, serosal eosinophilic infiltration is the rare,;t form of presentation, and may result in the development of eosinophilic ascites. Herein we repcrt an unusual case of eosinophilic gastroenteritis presenting with peritoneal eosinophilic infiltration diagnosed by a peritoneal biopsy. A 16-year-old woman came to our hospital presenting with abdminal <listensiron and tenderness, vomiting, and diarrhea with marked peripheral eosinophilia. Stool .;pecimens were negative for ova parasites. Biopsy specimens of esophagus, stomach, duodenum, and colon showed nonspecific intlammation but that of the peritoneum showed specific intense e.inophilic infiltration with fibrous band and eosinophilic vasculitis. A diagnosis of serosal eosinophil c gastroenteritis based on c]inical, laboratory, eosinophilic pertoneal fluid and histopathologic data, (:specially the biopsy specimens of the peritoneum. She was treated with corticosteroid and respond d dramatically with a complete resolution of ascites and other G-I symptoms. (Korean J Gastroenterol 1997; 30:547-552)
최웅송(Oung Seung Choi),박정영(Jong Young Park),이배진(Bai Jin Lee),이정호(Jung Ho Lee),김형기(Hyung Gi Kim),최낙현(Nak Hyun Choi),박봉수(Bong Sou Park),김시찬(Si Chan Kim),변동일(Dong Il Byun),김형길(Hyung Gil Kim),정동균(Dong Gyoon 대한내과학회 1994 대한내과학회지 Vol.47 No.6
N/A Osteopetrosis (also called Albers-Schoberg's disease, Marble bones and chalk bones) is a rare hone dysplasia in which, on the basis of a failure of osteoclastic and chondroclastic resorption, the bone become exceedingly dense. Two clinically distinct forms are now recognized and have different patterns of inheritance. The milder form is transmitted as an autosomal dominant trait and the more severe form is transmitted as an autosomal recessive trait. We have experienced a familial osteopertrosis, mother and three siblinges out of six, which was thought to be a autosomal dominant inheritance. We report a case of milder form of osteopetrosis with a review of literature.
박봉수(Bong Sou Park),박정영(Jung Young Park),이배진(Bai Jin Lee),이정호(Jung Ho Lee),김형기(Hyung Gi Kim),변동일(Dong Il Byun),김형길(Hyung Gil Kim),정동균(Dong Gyoon Jung) 대한소화기학회 1996 대한소화기학회지 Vol.28 No.6
Familial polyposis is an uncornmon hereditary disease characterized by the appearance of numerous polyps in the large intestine with a high potential for malignant transformation. If the patients were untreated, adenomatous polyp was developed to cancer. Therefore once the diagnosis is made, either total coloectomy or subtotal colectomy should be done as preventive measures. We experienced three cases of familial po]yposis which transformed to adeonocarcinoma. The diagnosis was rnade by familial history, morphologic findings of endoscopy and histologica.l study of the lesions. All of them were performed operative management and postoperative chemotherapy. We report our experiences of follow up of these cases and review with the disease reported in the literature. (Korean J Gastroenterol 1996;28:874 - 878)
이배진,변동일,김형길,정동균,최낙현,박정영 대한내과학회 1996 대한내과학회지 Vol.51 No.1
Hypothyroidism in frequently overlooked in the elderly because many of its symptoms are attributed to the normal aging process, Hypothyroidism may be accompanied by rheumatic syndromes such as neuropathy, myopathy, and arthropathy with chronic joint effusion. Because these symptoms are correlated with severity and durations of the hypothyroid state, early diagnosis may prevent severe articular sequelae. We experienced a case of primary hypothyroidism presenting with destructive arthropathy and thyroid replacement therapy was followed by longterm improvement.
허갑범,이현철,임승길,송영득,원영준,이유복,이배진,김준명 대한내분비학회 1997 Endocrinology and metabolism Vol.12 No.2
The relationship between hypercalcemic crisis and pancreatitis, first described in patients with hyperparathyroidism, still remains controversial. Acute pancreatitis may complicate the clinical course of hyperparathyroidism, particularly when the degree of hypercalcemia is severe. The incidence of hyperparathyroidism presenting as acute pancreatitis appears to be steadily decreasing, possibly reflecting the earlier diagnosis of asymptomatic hyperparaparathyroidism due to widespread application of screening methods. Here, we report two patients with primary hyperparathyroidism manifesting clinically as acute pancreatitis. One patient died of progessive pancreatitis and uncontrolled sepsis. The other patient was fullly recovered by emergent parathyroidectomy followed by medical management of hypercalcemia. (J Kor Soc Endocrinol 12:321-327, 1997)