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이인성,Lee, In-Seong 한국건강관리협회 1983 건강소식 Vol.7 No.2
이번호부터 새로 연재되는 의학상식 시리즈는 세계적 권위기관인 국제임상세포학회 평의원이며 미국임상병리학회 평의원인 이인성 박사가 집필해 주시기로 되었습니다. 이 박사는 또한 건협에서 실시하고 있는 자궁암검진사업의 판독을 담당하고 있는 권위자 입니다.
이인성,Lee, In-Seong 한국건강관리협회 1983 건강소식 Vol.7 No.3
지난 호부터 새로 연재되는 의학상식 시리즈는 세계적 권위기관인 국제임상세포학회 평의원이며 미국임상병리학회 평의원인 이인성 박사가 집필해 주시기로 되었습니다. 이 박사는 또한 건협에서 실시하고 있는 자궁암검진사업의 판독을 담당하고 있는 권위자 입니다.
이인성 대한흉부심장혈관외과학회 1986 Journal of Chest Surgery (J Chest Surg) Vol.19 No.2
Congenital cystic adenomatoid malformation [CCAM] of the lung is a rare but often fatal congenital lung bud anomaly that causes acute respiratory distress in the newborn infants. In those who survive infancy and early childhood, its clinical manifestations are not unusual to detect. Recently we experienced two children with CCAM; one with coughing and high fever, another without any symptom On case I, the patient was a 9 year-old female, and was suffered from coughing and high fever since 15 days before. Medical treatment was failed and then, exploratory thoracotomy was performed under the impression of loculated empyema. Finally, a right lower lobectomy was done with a satisfactory postoperative course. On case II, the patient was a 12 year-old female, and admitted for evaluation of known large pulmonary cyst which was checked at the outpatient clinic. Preoperative evaluations gave no more informations, so obliteration of cysts was performed with open biopsy. Two patients with CCAM are described in Korean Univ. Medical Center.
이인성 대한흉부심장혈관외과학회 1993 Journal of Chest Surgery (J Chest Surg) Vol.26 No.4
Aberrant right subclavian arteries were experienced in two young children. This is a rare aortic arch anomaly that usually does not produce symptoms. Symtomatic patients require surgical interventions.We describe two young children who had aberrant right subclavian artery with symptoms of difficulty in swallowing and respiratory problems. Diagnosis was made by esophagography, aortography and 3-Dimension chest CT. Operation had been advocated through right thoracotomy without difficulty for ligation, division and anastomosis to the ascending aorta. Dysphagia lusoria was immediately relieved and postoperative course was uneventful. We consider that the right thoracotomy is the choice of operative approach and noninvasive diagnosis by 3-Dimension chest CT is easily made for infant with aberrant right subclavian artery.