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소아에 (小兒) 있어서 간담도계의 (肝膽道系) 원발성 (原發性) 악성종양의 (惡性腫瘍) 임상적 (臨床的) 관찰
정재선(Jae Sun Jung),이인실(In Sil Lee),서정기(Jeong Kee Seo),안효섭(Hyo Seop Ahn),홍창의(Chang Yee Hong) 대한소화기학회 1983 대한소화기학회지 Vol.15 No.2
N/A The clinical data on the patients with primary malignant tumors of the hepatobiliary system from Aug 1968 to Sep 1983 have been reviewed. Eleven patients were hepatoblastoma, 4 patients were hepatocellular carcinoma and 1 patient was embryonal rhabdomyosarcoma occurred in common bile duct. Age incidence of the hepatoblastoma was younger than hepatocellular carcinoma. All 11 patients with hepatoblastoma were less than 3 years old, and 3 of the 4 patients with hepatocellular carcinoma were more than 3 years old. The prognosis of hepatocellular carcinoma occuring in children has been reported as poor, but several long-term survival cases have been reported after surgical resection in the hepatoblastoma. In 8 of the 16 cases, surgical resection was possible. Of the four long-term survivors of the hepatoblastoma, 2 patients has been alive for 10 months and 15 months since diagnosis till now.
유경희(Gyung Hi Yu),홍수종(Soo Jong Hong),김영휘(Yung Hwi Kim),박인숙(In Sook Park),문형남(Hyung Nam Moon),홍창의(Chang Yee Hong),유시준(Shi Joon Yoo) 대한소아알레르기호흡기학회 1994 소아알레르기 및 호흡기학회지 Vol.4 No.1
The Unilateral Absence of a Pulmonary Artery(UAPA) is an uncommon congenital anomaly. The diagnosis may be suspected from chest roentgenogram and confirmed by pulmonary arteriography. UAPA is frequently associated with other anomalies of the cardiovascular system such as patent ductus arteriosus and tetralogy of Fallot. When it occurs as an isolated anomaly, patients are more frequently asymtomatic, while and only a minority of cases develop pulmonary hypertension. We report an asymptomatic case of UAPA in an 1-year-old girl. Her chest X-ray revealed reduction of volume of right lung with shifting of the heart and mediastinum to the right side and elevation of the right hemidiaphragm. There was the differrence in the vascularity between the two lung fields, and the right hilar shadow was absent. Her lung perfusion scan revealed total perfusion defect of right lung. The diagnosis of UAPA was confirmed by pulmonary arteriography,
신생아에 심한 심부전증을 일으킨 선천성 뇌동정맥 기형: 풍선 색전 요법을 시도한 1례
박인숙,김영휘,홍창의,조영국,서대철,박영일 울산대학교 의과대학 1993 울산의대학술지 Vol.2 No.2
Cerebral arteriovenous malformation is a rare cause of congestive heart failure in neonates and is known to carry a very poor prognosis even wish prompt recognition and aggressive treatment. We recently encountered a 2-day-old male neonate with huge cerebral arteriovenous malformation who presented with intractable heart failure. Despite aggressive medical treatment and partial embolization with detachable balloon, baby died of severe hearts failure. Since there is no report of percutaneous balloon embolization in a neonate with this lesion in Korean literature, we wish to present our experience in one such neonate. Also we believe this is the first report of color Doppler findings in cerebral arteriovenous malformation in Korean literature.