http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
박찬금,류근신,김완섭,전석철,이중달,Park, Chan-Kum,Lyu, Geun-Shin,Kim, Wan-Sup,Jeon, Seok-Chol,Lee, Jung-Dal The Korean Society for Cytopathology 1997 대한세포병리학회지 Vol.8 No.1
저자들은 최근 면역기능이 저하되지 않은 50세 남자환자의 폐장에 국한되어 발생한 효모균증을 세침흡인 도말소견으로 진단하고 이의 세포도말 소견을 보고하는 바이다. 세침흡인 도말배경내에는 녹색 내지는 염색되지 않으며 굴절되어 보이는 다양한 크기의 둥글거나 난원형이면서 그 주변에 투명한 운륜을 갖는 균체가 다수 산재되어 관찰되었다. 균체의 크기는 $5{\sim}15{\mu}m$이었으며 Gomori methenaminesilver 염색상 발아성 홀씨가 잘 관찰되었다. Mucicarmine 염색상 피막은 연분홍색으로 염색되었다. Initial rapid diagnosis of primary pulmonary cryptococcosis(PPC) occurring in a immunocompetent host was made by transthoracic fine needle aspiration cytology of a solitary subpleural nodule. Numerous refractile spherical organisms surrounded by a clear halo were demonstrated with haematoxylin-eosin and Papanicolaou stains. The organisms, $5{\sim}15{\mu}m$ in diameter, were easily demonstrated with Gomori methenamine-silver stain. Many of the organisms showed narrow-base budding. Carminophilic cell walls were well demonstrated with mucicarmine stain.
김혁,이재원,이신영,전석철,강정호,지행옥,Kim, Hyuck,Lee, Jae-Won,Lee, Shin-Yeong,Jeon, Seok-Chol,Kang, Jung-Ho,Jee, Heng-Ok 대한흉부심장혈관외과학회 1987 Journal of Chest Surgery (J Chest Surg) Vol.20 No.3
A successful repair of traumatic descending thoracic aorta rupture was performed in a 27 year old man. The patient had automobile accident and transferred to our hospital. On admission, a chest film showed mediastinal widening and soon aortography was done. There was a fusiform aneurysm on the descending thoracic aorta just distal to the origin of the left subclavian artery measuring 5cm in diameter and 7cm in length. He underwent thoracotomy and the injured part of the aorta was replaced with a 24mm tightly Woven Dacron graft using femora-femoral bypass. The postoperative course was uneventful.
송동섭,정원상,김혁,김영학,강정호,이철범,전석철,이원미,홍은경,Song, Dong-Seop,Chung, Won-Sang,Kim, Hyuck,Kim, Young-Hak,Kang, Jung-Ho,Lee, Chul-Bum,Jeon, Seok-Chol,Lee, Won-Mi,Hong, Eun-Kyung 대한흉부심장혈관외과학회 2001 Journal of Chest Surgery (J Chest Surg) Vol.34 No.7
잘 분화된 태아성 선암종은 조직학적으로 폐모세포종과 유사하여, 폐모세포종의 한 분류로 생각되어지며, 육종성 형태와 상피성 형태 사이의 태아성 폐에 유사한 상피성 형태를 보인다. 최근 저자등은 19세 남자 환자에서 폐의 좌상엽 부위에 발생한 종괴에 미세 흡침 조직 검사상 폐모세포종으로 나와 좌상엽 절제술을 시행하였고, 술 후 시행한 조직 검사상 육종성 형태는 없었으며, 잘 분화된 태아성 선암종으로 확진되어 문헌고찰과 함께 보고하는 바이다. WDFA(Well-differentiated fetal adenocarcinoma) histologically resembles pulmonary blastoma. It is also thought to be a subtype of pulmonary blastoma, which has differentiated epithelial features resembling the fetal lung among its epithelial features and sarcomatous features. We recently encounted a patient who underwent surgery for WDFA. A 19-year-old man had a mass shadow in the upper lobe of the left lung. The tumor was diagnosed as pulmonary blastoma as a result of fine needle aspiration biopsy, and left upper lobe lobectomy was performed. No sarcomatous features was observed on postoperative histologic assessment, and the patient was diagnosed as having WDFA. This case is reported with a discussion of the literatures.
반동규,김혁,김영학,강정호,정원상,지행옥,이철범,전석철,Ban, Dong-Gyu,Kim, Hyuck,Kim, Young-Hak,Kang, Jung-Ho,Chung, Won-Sang,Jee, Heng-Ok,Lee, Chul-Bum,Jeon, Seok-Chol 대한흉부심장혈관외과학회 2001 Journal of Chest Surgery (J Chest Surg) Vol.34 No.10
만성 폐동맥 색전증은 비교적 드문 질환으로 저산소증과 폐동맥 고혈압을 일으켜 결국 호흡부전 및 우심부전을 초래한다. 급성 폐동맥 색전증 환자들은 대부분 혈전 방지제, 혈전용해제 등의 내과적 치료에 잘 치료되나 만성 폐동맥 색전증의 경우 섬유화된 혈전이 폐동맥벽에 견고히 붙어있어 내과적 치료에는 별 효과가 없어, 수술적 치료를 고려할 수 있겠다. 본원에서는 만성 폐쇄성 폐질환 및 만성 폐동맥 색전증으로 진단 받고 타 병원에서 수 차례 입원 치료를 받아 오던 47세 남자환자를 간헐적인 완전 순환 정지를 이용하여 폐색전증에 대한 내막 절제술을 시행하여 좋은 결과를 얻었기에 보고하는 바이다 Chronic pulmonary artery thromboembolism is a relatively rare phenomenon causing hypoxia and pulmonary hypertension that eventually leads to respiratory failure and right heart failure. Patients with acute pulmonary artery thromboembolism are generally treated with antithrombotics and thrombolytics. However, in cases with chronic pulmonary artery thromboembolism the fibrinized thrombus is so strongly adhered to the pulmonary artery wall that medical treatment becomes ineffective and surgical treatment must then be considered. We report a 47year old patient, with a history of repeated admission due to unresolved chronic obstructive pulmonary disease and chronic pulmonary artery thromboembolism at a local hospital, who underwent a successful endarterectomy of pulmonary artery thromboemboli using intermittent total circulatory arrest.
소아의 흉벽에 발생한 Langerhans 세포 조직구증의 치료 - 1례 보고 -
송동섭,지행옥,정원상,강정호,김영학,김혁,이철범,함시영,전석철,이원미,박찬금,Song, Dong-Seop,Lee, Heng-Ok,Chung, Won-Sang,Kang, Jung-Ho,Kim, Young-Hak,Kim, Hyuck,Lee, Chul-Bum,Ham, Shi-Young,Jeon, Seok-Chol,Lee, Won-Mi,Park, Chan-Kum 대한흉부심장혈관외과학회 2001 Journal of Chest Surgery (J Chest Surg) Vol.34 No.6
Langerhans 세포 조직구증(LCH, Langerhans\` Cell Histiocytosis)은 Langerhans\` cell histiocyte의 이상 증식을 특징으로 하는 원인 불명의 질환이다. 이 질환은 eosinophilic granuloma, Hand-Sch ller-Christian씨 병, Letterer-Siwe병을 포함하는 것으로 과거에는 histiocytosis X로 불리던 질환이다. 피부, 림프절, 골, 골수 및 체내 모든 조직과 기관을 침범할 수 있으나 국내에서 흉벽에서 발생된 예는 보고된 증례가 많지않다. 18개월 된 남자 환아에서 흉벽의 늑골에서 기원하여 골용해 소견을 동반한 종괴가 있어 수술적 절제한 후 LCH로 확진된 증례가 있어 문헌고찰과 함께 보고하는 바이다 Langerhans\` Cell Histiocytosis(LCH) is a disease of unknown origin, characterized by abnormal proliferation of Langerhans\` cells. Previously, it has been called histiocytosis X, which included eosinophilic granuloma, Hand-Sch ller-Christian\`s disease, and Letterer-Siwe disease. Any organs or tissues such as skin, lymph nodes, bone and bone marrow can be involved. However, LCH of chest wall is rarely reported in our country. We experienced a 18 month old male child, who had osteolytic lesion involving the rib with axillary lymph node metastasis. The tumor was confirmed as LCH after surgery.
우측상대정맥 없이 좌측 상대정맥이 좌심방으로 유입되는 활로씨 사징증의 수술치험 1례
김혁,김병일,김남수,김영학,정원상,강정호,지행옥,이철범,전석철,Kim, Hyuk,Kim, Byoung-Il,Kim, Nam-Su,Kim, Young-Hak,Chung, Won-Sang,Kang, Jung-Ho,Jee, Heng-Ok,Lee, Chul-Bum,Jeon, Seok-Chol 대한흉부심장혈관외과학회 1999 Journal of Chest Surgery (J Chest Surg) Vol.32 No.12
A persistent left superior vena cava draining into the coronary sinus is the most benign and widely encountered abnormality and can easily be explained embryologically as the persistence of the usual pattern of vnous circulation in the embryo,. However a persistent left superior vena cava draining into the left atrium with absent right superior vena cava is an extremely rare anomaly. We report this situation in an infant with tetralogy of Fallot. The most common approach has traditionally been intraatrial baffle repair to create a tunnel to the right atrium or rerouting of the left superior vena cava flow by directly anastomosing the left superior vena cava to the right atrium In the present study the left superior vena cava was transposed to the left pulmonary artery after the correction of tetralogy of Fallot. The most common approach has traditionally been intraatrial baffle repair to create a tunnel to the right atrium or rerouting of the left superior vena cava flow by directly anastomosing the left superior vena cava to the right atrium. In the present study the left superior vena cava was transposed to the left pulmonary artery after the correction of tetralogy of Fallot.
류마티스 관절염 환자에서 MTHFR 유전자 다형성과 경동맥 죽상경화증과의 관계
박재홍 ( Jae Hong Park ),( Ahmed El Sohemy ),강태영 ( Tae Young Kang ),정청일 ( Chung Il Joung ),전석철 ( Seok Chol Jeon ),이혜순 ( Hye Soon Lee ),엄완식 ( Wan Sik Uhm ),김태환 ( Tae Hwan Kim ),전재범 ( Jae Bum Jun ),유대현 ( D 대한류마티스학회 2003 대한류마티스학회지 Vol.10 No.3
Objective: Studies have suggested that the 5, 10-methylenetetrahydrofolate reductase (MTHFR) C677T mutation (alanine→valine) is a risk factor for atherosclerotic disease. We assessed the association between MTHFR gene polymorphism and carotid atherosclerosis in patients with rheumatoid arthritis (RA). Methods: Forty postmenopausal RA women (mean age: 58±5 years, mean duration of RA 14±5 years) treated with low dose methotrexate, other concurrent disease modifying anti-rheumatic drugs, non-steroidal anti-inflammatory drugs, steroid (prednisolone ≤5 mg/day) and folic acid (≥1 mg/day) were studied. The genetic polymorphism was detected by the polymerase chain reaction. We measured intima-media thickness (IMT) and plaques of the common carotid arteries by ultrasonography, and evaluated relations among the known risk factors for atherosclerosis, the genetic polymorphism, RA outcomes (Steinbrocker`s radiological stage and functional class defined by the ACR criteria) and markers of inflammation (erythrocyte sedimentation rate and C-reactive protein). Results: Among the 40 subjects, 12 had MTHFR genotype CC, 24 genotype CT, and 4 genotype TT. The frequencies of the MTHFR C and T allele were 0.6 and 0.4, respectively. Between the subjects with the CC genotype and those with the mutant T allele, there was no difference in age, body mass index, blood pressure (BP), lipid, duration of RA, RA outcome indices, rheumatoid factor, acute phase reactants and IMT. Carotid IMT was positively associated with age, systolic BP and antihypertensive drug use. There was no significant association between carotid IMT and the MTHFR C677T mutation. Conclusion: It is assumed that there was no significant relationship between the MTHFR C677T polymorphism and carotid atherosclerosis in Korean postmenopausal RA women.
1996년 춘계학술대회 학술퀴즈 : 다발성 임파절 이상증을 동반한 비대칭적 폐 간질성 병변
이경상 ( Kyung Sang Lee ),양석철 ( Suck Chul Yang ),윤호주 ( Ho Joo Yoon ),신동호 ( Dong Ho Shin ),박성수 ( Sung Soo Park ),이정희 ( Jung Hee Lee ),김혁 ( Hyuk Kim ),최요원 ( Yo Won Choi ),전석철 ( Seok Chol Jeon ) 대한결핵 및 호흡기학회 1996 Tuberculosis and Respiratory Diseases Vol.43 No.4