http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
최원석 ( Won Seok Choi ),박준오 ( Joon Oh Park ),정해원 ( Hae Won Jeong ),장태훈 ( Tae Hoon Jang ),윤원경 ( Won Kyoung Yun ),이지인 ( Ji In Lee ),박영석 ( Young Suk Park ) 대한내과학회 2008 대한내과학회지 Vol.75 No.3
십이지장의 원발성 편평세포암종은 매우 드문 종양이며 치료와 예후도 아직 잘 알려져 있지 않다. 최근 저자들은 복통을 주소로 내원한 44세 여자 환자를 복부 전산화 단층 촬영, 내시경, 전신 PET-CT 촬영을 통해 십이지장에서 발생한 원발성 편평세포암종으로 진단하였다. 환자는 수술을 하지 못하는 진행성 병변소견으로 고식적 항암치료를 시행하였으나 결국 악화소견을 보였으며, 이에 십이지장에서 발생한 편평세포암종을 문헌고찰과 함께 보고하는 바이다. Squamous cell carcinoma of the duodenum is an extremely rare neoplasm worldwide. A 44-year-old female patient was admitted to our institution for abdominal pain, and she was diagnosed with primary squamous cell carcinoma of the duodenum. The duodenal cancer was inoperable due to vascular invasion and regional lymph node metastasis. The patient was treated with palliative chemotherapy, but her disease progressed, and she was eventually referred to a local hospital for supportive care. The prognosis of squamous cell carcinoma of the duodenum is poor compared with that of usual duodenal adenocarcinoma. We report the details of this case of squamous cell carcinoma of the duodenum along with a review of the literature. (Korean J Med 75:349-353, 2008)
Budd-Chiari 증후군을 동반한 Churg-Strauss 증후군
장태훈 ( Tae Hoon Jang ),정해원 ( Hae Won Jeong ),최원석 ( Won Seok Choi ),윤원경 ( Won Kyoung Yun ),이진영 ( Jin Young Lee ),이병재 ( Byung Jae Lee ),최동철 ( Dong Chull Choi ) 대한천식알레르기학회 2007 천식 및 알레르기 Vol.27 No.3
Churg-Strauss syndrome (CSS) is a rare disease entity of unknown cause, which is characterized by systemic vasculitis, peripheral eosinophilia, extravascular granulomastosis and chronic atopic disease such as bronchial asthma. However, venous thrombosis is rarely reported in patients with Churg-Strauss syndrome. We report one patient with CSS who experienced obstruction of the hepatic and portal veins (Budd-Chiari syndrome). To our knowledge, this is the first report on the association between CSS and Budd-Chiari syndrome in Korea. (Korean J Asthma Allergy Clin Immunol 2007;27:181-185)
흉수를 동반한 Mycobacterium intracellulare 폐질환
곽수영 ( Soo Yeong Kwak ),배선윤 ( Sun Youn Bae ),윤원경 ( Won Kyoung Yun ),김민영 ( Min Young Kim ),김윤정 ( Yoon Jung Kim ),최문기 ( Moon Ki Choi ),고원중 ( Won Jung Koh ) 대한내과학회 2008 대한내과학회지 Vol.75 No.4
MAC은 NTM 폐질환을 일으키는 가장 흔한 원인균으로 만성폐쇄성폐질환, 기관지확장증 등 만성 호흡기질환을 가진 환자에서 많이 발생한다. 증상이 서서히 진행하는 경과와 함께 방사선학적으로는 상엽에 공동을 보이거나 기관지확장증에 동반된 다발성 결절이 특징적이다. 저자들은 기관지확장증을 가진 환자에서 흉수를 동반한 M. intracellulare 폐질환 증례를 경험하여 이를 보고하는 바이다. Nontuberculous mycobacterial infection is rarely accompanied by pleural involvement. We report a very rare case of Mycobacterium intracellulare pulmonary disease accompanied with pleural effusion. A 76-year-old man was admitted to our hospital because of dyspnea. A chest radiograph and CT showed bilateral bronchiectasis and bronchopneumonia accompanied with right pleural effusion. The fluid was lymphocyte-dominant exudative effusion, and microbiological examinations of the effusion, including staining and culturing, proved negative. However, one month after admission, subsequent cultures of bronchial washing fluid revealed the presence of M. intracellulare. The patient`s effusion was gradually resolved with antibiotic treatment, including clarithromycin. (Korean J Med 75:475-478, 2008)