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이광섭 ( Lee Gwang Seob ),김신응 ( Kim Sin Eung ),김성림 ( Kim Seong Lim ),최광섭 ( Choe Gwang Seob ),장미영 ( Jang Mi Yeong ),김종만 ( Kim Jong Man ),이효진 ( Lee Hyo Jin ) 대한내과학회 1992 대한내과학회지 Vol.42 No.4
Squamous cell papilloma is a rare benign esophageal tumor which is usually small asymptomatic and is an incidental finding at esophagogastric endoscopy. It is important to confirm the diagnosis of esophageal papilloma histologically since this lesion may be confused with verrucous carcinoma of the esophagus on visual inspection. A case of 26-year-old man with epigastric pain and discomfort but no dysphagia was experienced. During endoscopy, small warty tumor with 1㎝ in size was found at 24㎝ portion of the incisor incidentally and biopsy turned out to be squamous cell papilloma on the esophagus.
진균구로 오인된 낭포내 응혈을 보인 23세 여자에서의 선천성 낭포성 유선종 폐기형 1례
이강룡 ( Gang Ryong Lee ),이군순 ( Kun Sun Lee ),주인규 ( In Kyu Joo ),박준옥 ( June Ock Park ),최승준 ( Seung Jun Choi ),이원석 ( Won Seok Lee ),김의숙 ( Eui Sook Kim ),이규현,김대하 ( Dae Ha Kim ),이광섭 ( Gwang Seob Lee ),한영숙 ( 대한결핵 및 호흡기학회 1999 Tuberculosis and Respiratory Diseases Vol.46 No.1
진균구로 오인된 낭포내 응혈을 보인 23세 여자에서의 선천성 낭포성 유선종 폐기형 1례
이강룡,이군순,주인규,박준옥,최승준,이원석,김의숙,이규현,김대하,이광섭,한영숙,지미경,박정웅,Lee, Gang-Ryong,Lee, Kun-Sun,Joo, In-Kyu,Park, June-Ock,Choi, Seung-Jun,Lee, Won-Seok,Kim, Eui-Sook,Lee, Gyu-Hyeon,Kim, Dae-Ha,Lee, Gwang-Seob,Han, 대한결핵및호흡기학회 1999 Tuberculosis and Respiratory Diseases Vol.46 No.1
We describe unusual manifestations of congenital cystic adenomatoid malformation (C.C.A.M.) of the lung, such as movable fungal ball-like intracystic blood clots and hemoptysis, which were detected in previously healthy 23 years-old woman. We identified blood clots only after left upper lobectomy and could not distinguish from fungal ball with radiographic methods. CCAM of the lung, rare and lethal form of congenital pulmonary cystic disease, was initially introduced by Ch, in and Tang in 1949. The histogenesis of this lesion is characterized by polypoid glandular tissue proliferation and overgrowth of mesenchymal elements due to cessation of bronchiolar maturation which occurred in after 16weeks intrauterine period. In 80-95% of reported cases, the lesion was confined to a single lobe and there was no lobe and right and left lung predilection The clinical presentation may be widely variable, ranging from intrauterine fetal death to late discovery in childhood with recurrent pulmonary infection. But there,s no reports which were misdiagnosed with intracystic fungal ball. The treatment choice is lobectomy of affected lobe. There,s a few case reports with rhabdomyosarcoma, bronchiolar cell carcinoma and myxosarcoma arising in CCAM patients. Therefore, early resection is recommended even if asymtomatic cases. We experienced a rare case of CCAM of the lung in 23 years old female, and there were intracystic fungal ball-like movable blood clots in lower portion of left lung. After left upper lobectomy was performed, now she is discharged and followed up without any complications.
김신응(Sin Eung Kim),이광섭(Gwang Seob Lee),선우인철(In Chul Sunwoo),조준길(Joon Gil Cho),장미영(Mi Young Jang),김종만(Jong Mann Kim),홍선미(Sun Mee Hong) 대한내과학회 1992 대한내과학회지 Vol.43 No.6
The tissue damage associated with an electrical injury occurs when electric energy is converted to thermal energy or heat according to Joule's law, and it occurs not only cutaneous contact site but may also involve underlying tissue and organs along the route taken by the current between the entrance and exit sites. Among multiple interacting variables, inc1uding voltage, amperage, tissue resistance, type of current and current pathway, amperage is most important factor which relates closely to deep tissue injury and mortality. A case of 33 year old laborer with left hemiplegia after electric current of AC 380 voltage, 60 Hz was experienced. Normal initial brain CT scan turned out to have right hemorrhagic infarct 5 days later, and decreased infarct size 2 months later, with neurological sequelae of left hemiplegia.
다발성 소방이 형성된 결핵성 흉막염 환자에서 경부에 결핵성 단일 한성농양을 보인
이정아 ( Jeong Aa Lee ),김의숙 ( Eui Sook Kim ),백영주 ( Young Joo Baek ),이광섭 ( Gwang Seob Lee ),선우인철 ( In Cheol Sunwoo ),김대하 ( Dae Ha Kim ),장지정 ( Jie Jeong Jang ),박석민 ( Suck Min Park ),지미경 ( Mi Kyung Ji ) 대한결핵 및 호흡기학회 1996 Tuberculosis and Respiratory Diseases Vol.43 No.3
폐렴을 동반한 15 세 남자 환자에서 발견된 선천성 낭포성 유선종 폐기형 1 예
백영주(Young Joo Baek),이정아(Jeong Aa Lee),김의숙(Eui Sook Kim),이원석(Won Seok Lee),이강룡(Kang Ryang Lee),이광섭(Gwang Seob Lee),김신응(Synn Eung Kim),선우인철(In Cheol Sunwoo),김대하(Dae Ha Kim),장지정(Jie Jeong Jang),한영숙(Young 대한내과학회 1997 대한내과학회지 Vol.52 No.1
Congenital cystic adenomatoid malformation(C.C. A.M.) is a rare variant of congenital pulmonary cystic diseases. C.C.A.M. was first distinguished from other pulmonary cystic lesions by Ch`in and Tang in 1949. It is characterized by cessation of bronchiolar maturation with an overgrowth of mesenchymal elements and proliferation of polypoid glandular tissue in the absence of normal alveolar differentiation. In 80% to 95% of cases, C.C.A.M. of the lung is confinded to a single lobe and there is no lobe predilection and right and left predominance. The clinical presentation may be widely variable, ranging from intrauterine fetal death secondary to nonimmune hydrops fetalis to discovery in childhood after recurrent pulmonary infections. Definitive treatment is removal of affected lobe. In rare instances, there is cases of myxosarcoma, embryonal rhabdomyosarcoma. Bronchoalveolar carcinoma arising in C.C.A.M.. So, resection is recommended even if they are asymtomatic. We have experienced a case of congenital cystic adenomatoid malformation (type II) of the lung in 15 year old man with pneumonia. After the improvement of pneumonia, surgical operation was performed. A brief review of the related literature is presented.
이달의 x-선 : 흉부 X-선상 속립성 결핵과 유사한 양상을 보인 Mycoplasma 폐렴에서 ARDS로 진행된 1예
김의숙 ( Eui Sook Kim ),이원석 ( Won Seok Lee ),이강룡 ( Kang Ryung Lee ),이정아 ( Jeong Aa Lee ),백영주 ( Young Joo Baek ),이광섭 ( Gwang Seob Lee ),선우인철 ( In Cheol Sunwoo ),김대하 ( Dae Ha Kim ),장지정 ( Jie Jeong Jang ) 대한결핵 및 호흡기학회 1996 Tuberculosis and Respiratory Diseases Vol.43 No.4
전자 현미경상 Epinephrine 과립이 관찰된 Zuckerkandl 기관에 발생한 Norepinephrine 분비성 갈색세포종 1예
이원석,김의숙,이강룡,이정아,장지정,선우인철,김대하,이광섭,백영주 대한내분비학회 1996 Endocrinology and metabolism Vol.11 No.2
Extraadrenal pheochromocytomas developed from the paraganglia other than adrenal medulla are uncommon tumors. Such lesions have been reported that as much as 10% of retroperitoneal paragliomas arise outside the adrenal gland. But their incidence and prognosis are changing partly as a result of progression in developmental mechanism, diagnostic tools and concepts including ultrastructure, immunohistochemistry. The ultrastructure of chromaffine neoplasm from adrenal and extraadrenal tissues has been studied with chrornaffine granule specificity and type of catecholamine content. With rare exceptions, extraadrenal chrornaffine tumor mainly has high concentration of norepinephrine which is suggested as dict relationship to numoruos electrone dense granular bodies in the cell cytoplasrm. High or intermediate level of epinephrine in tissue is associated with cytoplasmic granular bodies of much less density. Recently we experienced the exception, a case of norepinephrine secreting pheochrom-ocytoma in the organ of Zuckerkandl with epinephrine granules in cytoplasm and this discrepancy probably due to the plasticity - the differences in developmental process and local factors between adrenal medulla and extraadrenal tissues(J Kor Soc Endocrinol 11:233 ~239, 1996).