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박의련(Eui Ryun Park),이동기(Dong Ki Lee),이상철(Sang Cheol Lee),김영경(Young Kyung Kim),김준명(Jun Myeung Kim),박성진(Sung Jin Park),홍사준(Sa Joon Hong),권상옥(Sang Ok Kwon) 대한내과학회 1996 대한내과학회지 Vol.50 No.5
N/A Objectives: The aim of this study was to investigate the prevalence of alcoholic chronic pancreatitis in alcoholic liver disease and the relationship between the degree of pancreatitis and the pathologic type of alcoholic liver disease. Methods: We reviewed ERCP in 68 patients with alcoholic liver disease who were clinically suscepted as alcoholic chronic pancreatitis. Alcoholic liver disease was diagnosed by liver biopsy and alcohol history. Alcoholic chronic pancreatitis was diagnosed by ERCP and grouped by severity according to Anacker and Loffler`s classification, Results: Pancreatic duct changes suggesting alcoholic chronic pancreatitis were present at ERCP in 31.5% of the biopsy-confirmed alcoholic liver disease. There was no correlation between the histopathologic classification of alcoholic liver disease and the severity of alcoholic chronic pancreatitis. Conclusion: In alcoholic liver disease, the possibility of alcoholic chronic pancreatitis should always be considered.
송창호,정춘희,박의련,원영준,신영구,이미덕,강성준,변주원,최윤종,조미연 대한내분비학회 1996 Endocrinology and metabolism Vol.11 No.3
Pheochromocytoma is a catecholamine producing turnor and raise with less than 0.1% of hypertensive patients. It is developed, most commonly, in sporadic pheochromocytoma or multiple endocrine neoplasia type 2. Therefore, when hypercalcitoninemia is found in a patient with pheochromocytoma, the possibility of multiple endocrine neoplasia type 2 or the ectopic secretion of calcitonin must be considered. Recently we experienced a 45 year old male patient with sporadic pheochrornocytoma. He also had hypercalcitoninemia and normocalcemia. After the removal of pheochromocytoma, serum calcitnnin level returned to normal. Secretion of calcitonin was confirmed by immunohisto- chemical stain(J Kor Soc Endocrinol 11:343-347, 1996).
공터키안을 동반한 쉬한 증후군에서 그레이보스 병이 병발된 2예
최윤종,정춘희,박의련,김홍승,신영구 대한내분비학회 1996 Endocrinology and metabolism Vol.11 No.4
The empty sella syndrome is characterized by obesity, frequent pregnancy, headache and high blood pressure, but its exact cause remains unknown. Usually the incomplete diaphragmatic sella has been considered as the cause of the empty sella syndrome, but some authors recently have suggested that the antipituitary antibody way be related to development of pituitary atrophy and the pituitary empty sella syndrome, and thus it may be clinically useful as screening test for the empty sella syndrome. We experienced two empty sella syndromes associated Graves disease and applied the antipituitary antibody as the diagnostic tool of the empty sella syndrome. But none of this two patients had antipituitary antibody and we report these cases with reviews of literatures. (J Kor Soc Endoerinol 11:517~522, 1996)