http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
D - Penicillamine에 의한 담즙 정체성 황달
이준상(Joon Sang Lee),백옥지(Ok Ji Paik),김한성(Han Sung Kim),박성수(Sung Su Park),한경근(Kyung Keun Han),박양훈(Yang Hun Park),제영성(Yeong Sung Jae),박욱화(Wook Hwa Park) 대한소화기학회 1993 대한소화기학회지 Vol.25 No.4
Since 1966, D-Penicillamine has been used in the management of scleroderma. However, its therapeutic usefulness has been limited by a high incidence of a variety of adverse reactions. Cholestatic jaundice secondary to D-Penicillamine administratiori has been reported infrequently. We have experierced a case of acute chotestatic jaundice in a patient with scleroderma treated with D- Fenicillamine. We have encountered a patients who recovered from this complication whn D Penicillamine therapy was withdrawn. Literature was re!iewed briefly.
최정숙(Jeong Sug Choi),류수현(Su Heon Ryu),유대성(Dae Seong Yu),오정열(Jeong Yeol Oh),김영묵(Young Mook Kim),이충원(Choong Won Lee),제영성(Yeong Sung Jae),이준상(Joon Sang Lee) 대한소화기학회 1995 대한소화기학회지 Vol.27 No.3
Hepatosplenic tuberculosis is manifested commonly as miliary form, but the isolated form of hepatosplenic tuberculosisis is extremity rare. The local form of hepatosplenic tuberculosis is trans- ported to liver from intestine through portal vein. Basic pathology is granuloma. We described a patient with tuberculous abscess of liver and spleen proved by computed tomography and microbial identification. Liver specimen obtained by CT-guided fine needle aspiration showed Mycobacterium tuberculosis. After one month of antituberculous medication, the patients condition has been improved. Thus, the local form of hepatic tuberculosis must be differentiated from similar diseases, because it can be cured dramatically by antituberculous medication. (Korean J Gastroenterol 1995;27:363 - 368)
Primary Empty Sella Syndrome 에 동반된 뇌하수체 기능저하중 및 중추성 요붕증 1 예
최정숙,김한성,권기호,박양훈,제영성,이복근,서보정,오정열 대한내과학회 1994 대한내과학회지 Vol.47 No.2
The empty sella syndrome results from and extension of the subarachnoid space into an intrasellar portion with expansion of sella and flattening of the pituitary gland. The empty sella syndrome is distinguisted between $quot;primary$quot; (without prior surgical or radiotherapeutic procedurea) and $quot;secondary$quot; (following such procedure) cases. In this syndrome, the endocrine function is usually normal and this syndrome which is accompanied with endocrinologic abnormalities and diabetes insipidus is rarely reported. We discribed a patients of central type of diabetes insipidus, hypoptuitarism including growth retardation and sexual infantilism in the primary empty sella syndrome. So we present this case with a review of the literature.