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진행성 대장암 환자에서 Oxaliplatin과 UFT, Leucovorin 복합화학요법의 효과
신진향 ( Jin Hyang Shin ),김소연 ( So Yeon Kim ),우창민 ( Chang Min Woo ),김영섭 ( Young Sup Kim ),김지영 ( Ji Young Kim ),서정현 ( Jung Hyun Seo ),이완석 ( Wan Suk Lee ),배성화 ( Sung Hwa Bae ),류헌모 ( Hun Mo Ryoo ),이한일 ( Han 대한내과학회 2004 대한내과학회지 Vol.67 No.1
목적: UFT와 경구용 leucovorin (LV) 요법은 진행성 대장암 환자의 치료에서 5-Flurouracil/LV 급속 정주법과 같은 효과를 보이면서 더 안전하고 편리하다. 저자들은 진행성 대장암 환자에서 oxaliplatin과 UFT/LV 요법의 효과와 안전성을 조사하였다. 방법: 1999년 1월부터 2001년까지 전이성 또는 재발성 대장암으로 진단받았던 28명의 환자를 대상으로 하였다. 치료 방법은 제 1일에 oxaliplatin 130㎎/㎡을 Background: UFT/oral leucovorin (LV) provided a safer, more convenient oral alternative to bolus i.v. 5-Fluorouracil/LV regimen for advanced colorectal cancer while producing equivalent survival. We evaluated the efficacy and safety of a combination of ox
IgA 신병증을 동반한 쇼그렌증후군과 피부근염의 중복증후군
신진향 ( Jin Hyang Shin ),박근우 ( Keun Woo Park ),조자경 ( Ja Kyoung Cho ),한석재 ( Seok Jae Han ),정승혜 ( Seung Hie Chung ),김채기 ( Chae Gi Kim ),최정윤 ( Jung Yoon Choe ),김상경 ( Sang Gyung Kim ) 대한류마티스학회 2005 대한류마티스학회지 Vol.12 No.4
An overlap syndrome is used to describe patients who have two or more well-defined connective tissue diseases such as rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), systemic sclerosis (SSc), and polymyositis. Their coexistence is defined clinically and often by specific serologic tests. We report a case of dermatomyositis associated with IgA nephropathy that had overlapping features of Sjogren`s syndrome. This dermatomyositis and Sjogren`s overlap is a rarely reported overlap syndrome worldwide.
장천공과 누공을 동반한 베체트 장염 환자에서 수술 후 Infliximab으로 치료한
최우영 ( Woo Young Choi ),최정윤 ( Jung Yoon Choe ),이주형 ( Joo Hyoung Lee ),서창진 ( Chang Jin Seo ),박근우 ( Keun Woo Park ),김지영 ( Ji Young Kim ),박성훈 ( Sung Hoon Park ),신진향 ( Jin Hyang Shin ) 대한류마티스학회 2007 대한류마티스학회지 Vol.14 No.1
Behcet`s disease is a chronic, relapsing vasculitis of unknown origin that affects nearly all organs. The most frequent extra-oral sites of gastrointestinal involvement are the ileocecal lesion and the colon. The lesions are typically resistant to medical treatment and frequently recur with surgical treatment. We describe a patient who had intestinal Behcet`s disease complicated perforation and enterocutanous fistula with a good response to infliximab.
김현숙 ( Hyun Sook Kim ),박근우 ( Keun Woo Park ),김수경 ( Soo Kyoung Kim ),김지영 ( Ji Young Kim ),박성훈 ( Sung Hoon Park ),신진향 ( Jin Hyang Shin ),김상경 ( Sang Gyung Kim ),최정윤 ( Jung Yoon Choe ) 대한류마티스학회 2007 대한류마티스학회지 Vol.14 No.2
Adult onset Still`s disease is an rare inflammatory disease with the characteristic of fever, skin rash, arthralgia or arthritis, lymphadenopathy, leukocytosis and multiple systemic organ involvement. Its accurate pathogenesis has not been elucidated yet. Its clinical manifestation is also very diverse, from relatively mild symptoms to severe complications such as concomitant infection, liver failure, disseminated intravascular coagulation, myocarditis, adult respiratory distress syndrome, which may lead to death in some cases. Particularly, concomitant hemophagocytic syndrome is rare complication that could induce a fatal outcome. Thus it is important to diagnose early and start treatments. Until now, it has been reported in only one case of adult onset Still`s disease in Korea. Here, we report two female cases of adult onset Still`s disease with concomitant hemophagocytic syndrome.