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폐암진단을 위한 객담세포검사 결과 - 16개월간의 전주 예수병원 객담세포검사 결과를 바탕으로 -
이혜경,이광민,정동규,강대송,김귀완,Lee, Hye-Kyung,Lee, Kwang-Min,Chung, Dong-Kyu,Kang, Dae-Song,Kim, Kwi-Wan 대한세포병리학회 1994 대한세포병리학회지 Vol.5 No.2
A prospective survey of sputum cytologic specimen was performed for 16 months from Jan. 1993 to Apr. 1994 in Presbyterian Medical Center. The purpose of this study is to find the positive rate of sputum cytology in the diagnosis of lung cancer and to correlate these results with tumor location and stage. Sputum cytologic specimen were received from 104 patients among 158 patients diagnosed as lung malignancy by histologic examination. Cytologic diagnosis of "suggestive of malignancy" was made in 61 patients (59%) and dysplasia in 9 patients(9%), atypia in 14 patients(13%), benign in 15 patients(14%) and inadequate specimen in 5 patients (5%), respectively. Among 84 patients beyond the cytologic diagnosis of atypia, 51 patients (61%) disclosed a central location, while 33 patients (39%) showed peripheral lesions. All 54 patients diagnosed as suggestive of non-small cell carcinoma were stage III or over, and all 7 patients diagnosed as suggestive of small cell carcinoma were in advanced stage. These results suggest that the cytologic examination of sputum seems to be an important tool in diagnosis of lung cancer.
고요산 혈증을 나타낸 부분적 Hypoxanthine Guanine Phosphoribosyltransferase ( HGPRT ) 결핍 1 예
허원영(Weon Young Huh),신성혜(Sung Hye Shin),이순형(Soon Hyung Lee),양성욱(Seong Wook Yang),강대송(Dae Song Kang),김미애(Mi Ae Kim),이용웅(Yong Ung Lee),이광영(Kwang Young Lee) 대한내과학회 1995 대한내과학회지 Vol.48 No.5
Hypoxanthine-guanine phosphoribosyltransferase deficiency is an inborn error of purine metabolism, and transmitted by X-linked recessive trait. complete deficiency of the enzyme causes the Lesch-Nyhan syndrome which is characterized by hyperuricemia, hyperuricaciduria, severe neurologic dysfunction including hyper-reflexia, choreo-athetosis, mental retardation and self mutilation. Partial deficiency of the enzyme causes uric acid overproduction and uric acid nephrolithiasis, but does not manifest neurologic dysfunction. We report a case of partial hypoxanthine-guanine phosphoribosyltransferase deficiency. The enzyme activity, measured by high performance liquid chromatography from erythrocyte lysate, was 23.7% of normal control. The patient exhibited hyperuricemia, bladder stone, and growth retardation, without neurologic manifestation.
조진웅(Chin Woong Cho),김병구(Byoung Ku Kim),최수영(Su Young Choi),이태헌(Tae Hun Lee),김미애(Mee Ae Kim),강대송(Dae Song Kang),이순형(Sun Hyoung Lee),김귀완(Kwi Wan Kim),이광민(Kwang Min Lee) 대한내과학회 1995 대한내과학회지 Vol.48 No.6
Primary pulmonary amyloidosis is a rare disorder. It can be classified into tracheo-bronchial, diffuse alveolar septal and nodular parenchymal form. Tracheo-bronchial amyloidosis can be further subdivided into submucosal plaques and pseudotumorial mass. We report a case of pseudotumorial tracheo-bronchial amyloidosis in a 61year-old woman confirmed by bronchofiberscopic biopsy. She has suffered from cough and sputum for 3 months, and recently triangular hazy density in right perihilar area was found on chest X-ray with aggravation of symptoms. The chest CT showed a collapse in superior segment of right lower lobe and pleural thickening with multiple calcifications in posterior pleura of left lower chest. The bronchofiberscopic findings showed that the superior segmental bronchus of right lower lobe was completely obstructed and a solitary mass was in the orifice of right intermedius bronchus. The bronchoscopic biopsy revealed amyloid depositions beneath bronchial mucosa. We discuss this case with review of literature.