http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
류한작,한지숙,김유선,박기일,양우익,이종두 연세대학교의과대학 2004 Yonsei medical journal Vol.45 No.SUP
Posttransplant lymphoproliferative disorder (PTLD) is a serious complication of organ transplantation. PTLD is the disorder arising from the combined effects of Epstein-Barr virus associated lymphoid proliferation with the disruption of the normal immune control by the cytotoxic T cells. The treatment for PTLD is one of the most controversial topics in solid organ transplantation. It is well known that the initial management of PTLD is a reduction of immunosuppression. Early diagnosis and the early reduction in immunosuppression are essential even for monomorphic lymphoma. We report here on a case of the complete resolution of PTLD (diffuse large B cell lymphoma) which occurred after a drastic reduction of immunosuppression in a renal transplant recipient.
Hepatic Artery Pseudoaneurysm Associated with Plastic Biliary Stent
박정엽,류한작,방승민,송시영,정재복 연세대학교의과대학 2007 Yonsei medical journal Vol.48 No.3
The increased use of interventional procedures and laparoscopic cholecystectomy in the management of hepatobiliary disorders is associated with an increased incidence of hemobilia and hepatic artery aneurysm. Here we report a case of hepatic artery pseudoaneurysm associated with a plastic biliary stent. Multiple factors were involved in the formation of the hepatic artery aneurysm (HAA) and it was successfully treated by embolization.
춘계학술대회 : 포스터발표 ; 간 절제술을 시행받은 간세포암 환자에서 수술 전 α-Fetoprotein과 PIVKA-2 양성 여부와 수술 후 임상 경과
안상훈,류한작,김자경,김도영,김지현,한광협,백용한,이관식,문병수,전재윤,문영명 대한간학회 2005 Clinical and Molecular Hepatology(대한간학회지) Vol.11 No.3(S)
배경/목적: 간세포암의 종양표시자로서 α-Fetoprotein (AFP)과 Prothrombin induced by vitamin K absence or antagonist-II (PIVKA-II)가 유용하게 쓰이고 있다. 하지만 AFP 또는 PIVKA-II를 생성하는 간세포암의 임상적 차이에 대해서는 아직 밝혀진 바가 많지 않다. 본 연구는 간세포암 절제 후 예후 인자로서 수술 전 혈청 AFP과 PIVKA-II 양성 여부에 따른 수술 후 임상적 경과를
강신욱,김영리,김현욱,권영은,류동열,이미정,박경숙,류한작,박정탁,오형중,한승혁,유태현 연세대학교의과대학 2016 Yonsei medical journal Vol.57 No.5
Purpose: Despite new treatment strategies, anemia remains the most prevalent complication in patients with end-stage renal disease (ESRD). We investigated whether 25-hydroxyvitamin D [25(OH)D3] deficiency was associated with anemia in ESRD patients. Materials and Methods: We reviewed the medical records of 410 ESRD patients who had undergone renal transplantation (RTx) at Yonsei University Health System and who had 25(OH)D3 levels measured at the time of RTx. Patients were divided into two groups based on baseline 25(OH)D3 concentrations: group 1, 25(OH)D3 levels <10 ng/mL; and group 2, 25(OH)D3 levels ≥10 ng/mL. Results: Using multivariate regression models, 25(OH)D3, age, and erythrocyte-stimulating agent (ESA) dose were found to be significantly associated with hemoglobin (Hb) levels [25(OH)D3: β=0.263, p<0.001; age: β=0.122, p=0.010; ESA dose: β=-0.069, p=0.005]. In addition, logistic regression analysis revealed that patients in group 1 had a significantly higher risk for developing anemia (Hb level <10 g/dL) compared to group 2 patients, even after adjusting for potential risk factors for anemia (odds ratio=3.857; confidence interval=1.091–13.632; p=0.036). Conclusion: 25(OH)D3 deficiency was significantly associated with anemia in patients with ESRD. Randomized controlled trials are needed to determine whether vitamin D supplementation can improve anemia in these patients.
급성 A형 전격성 간염 (Fulminant Hepatitis)과 동반된 급성 신부전증
이동형 ( Dong Hyung Lee ),김자경 ( Ja Kyung Kim ),정현수 ( Hyun Soo Chung ),류한작 ( Han Jak Ryu ),문성진 ( Sung Jin Moon ),안상훈 ( Sang Hoon Ahn ),전재윤 ( Chae Yoon Chon ),한대석 ( Dae Suk Han ),강신욱 ( Shin Wook Kang ) 대한신장학회 2006 Kidney Research and Clinical Practice Vol.25 No.1
증례 : 선천적 배측 췌장 부분 발육 부전증과 동반된 Castleman 병 1예
박수영 ( Soo Young Park ),방승민 ( Seung Min Bang ),김명환 ( Myoung Hwan Kim ),류한작 ( Han Jak Ryu ),정재복 ( Jae Bock Chung ),이우정 ( Woo Jung Lee ),송시영 ( Si Young Song ) 대한내과학회 2006 대한내과학회지 Vol.71 No.1
배측 췌장의 발육 부전증은 배측 원기로부터 유래하는 췌장의 체부와 미부가 형성되지 않는 매우 드문 췌장의 선천적 기형이다. Castleman 병 역시 매우 드문 림프절 종양으로 일반적으로 종격동에서 호발하나 후복막강의 췌장 미부 위치에서 발견된 예는 흔하지 않다. 배측췌장 발육 부전증과 췌장 미부에 위치하는 Castleman병이 한 환자에서 동시에 발견된 예는 아직 보고된 바 없다. 저자들은 췌장의 부분 발육 부전증이 있는 환자에서 마치 췌장 미부의 종양처럼 보이는 Castleman 병을 영상학적 검사와 수술 및 조직 검사를 통해 확진하였기에 이를 보고하는 바이다. Agenesis of dorsal pancreas is a very rare congenital anomaly which comes from the failure of development of the body and tail of pancreas in embryogenesis. Castleman`s disease is a rare lymphoid tumor which usually occurred in the mediastinum, but it is very uncommon in the retroperitoneal pancreatic tail area. We report a case of partial agenesis of dorsal pancreas with Castleman`s disease in pancreatic tail area, mimicking a pancreatic tumor. A 46-year-old woman was admitted to our hospital with intermittent abdominal discomfort for 2 months. Computed tomography, magnetic resonance imaging, and endoscopic retrograde cholangiopancreatography (ERCP) revealed a tumor at distal pancreatic tail area, short pancreatic duct, and absence of pancreatic body and tail. The surgical excision of the tumor revealed hyaline-vascular type Castleman`s disease.(Korean J Med 71:80-85, 2006)