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목단피(牧丹皮)가 천식(喘息)유발 cytokine 분비와 호산구 chemotaxis에 미치는 영향
문성훈,정승기,이형구,정희재,Moon, Sung-Hun,Jung, Sung-Ki,Rhee, Hyung-Koo,Jung, Hee-Jae 대한한방내과학회 2005 大韓韓方內科學會誌 Vol.26 No.1
Objective : Airway inflammation is now regarded as a defining feature of asthma. The importance of eosinophits in the airway inflammation of asthma patients is widely recognized, and eosinophils mobilization in the respiratory epithelium is activated by chemoattractants and cytokines. This study was designed to examine the extent of the ability of Moutan Cortex Radicis to inhibit eosinophil chemotaxis of pulmonary epithelium after allergic stimulation. Material and Methods : Water extracts of Moutan Cortex Radicis and pulmonary epithelial cell lines A549(human type II-like epithelial cells) and human eosinophils were used. Cytotoxic effects of Moutan Cortex Radicis were estimated via MTS assay, and the effects of Moutan Cortex Radicis on chemokines from prestimulated A549 cells were estimated by sandwich ELISA and RT-PCR. Chemotaxis assay on prestimulated eosinophils treated with Moutan Cortex Radicis. was conducted Result : In this study we demonstrated that $TNF-{\alpha}$ and IL-4, $IL-1{\beta}$ induced the accumulation of chemokines' mRNA in the pulmonary epithelial cell lines A549 in a dose-dependent manner. Chemokines of eotaxin, ICAM-1, YCAM-1, IL-8, IL-16 were inhibited by Moutan Cortex Radicis in a dose dependent manner, but RANTES showed no inhibition due to Moutan Cortex Radicis. Eosinophil migration was inhibited at high concentrations of Moutan Cortex Radicis. Conculusion : These findings are indicative of supression of chemokines accomplished by Moutan Cortex Radicis treatment, demonstrating the potential therapeutic value of Moutan Cortex Radicis for treating diseases such as asthma.
문성훈(Sung Hun Moon),최해종(Hae Jong Choi),윤욱돈(Uk Don Yun),양두경(Doo Kyoung Yang),우영석(Young Seok Woo),장광열(Kwang Yul Chang),지삼룡(Sam Ryong Jee),오일환(Il Hwan Oh),김성은(Seong Eun Kim),김기현(Ki Hyun Kim) 대한신장학회 2001 Kidney Research and Clinical Practice Vol.20 No.1
Tuberous sclerosis is a rare disease, which occurs sporadically or hereditarily and is recognized by its neurological and dermatological manifestations and may be accompanied with renal anomalies. The cla- ssical triad is composed of seizure, mental retardation and adenoma sebaceum on face. We experienced two cases of tuberous sclerosis in sporadic forms by mutation without any familial history which suggests the diseases were occurred by mutation rather than by autosomal dominant inheritance. In the first case, a 24-year-female patient with hypertension and abnormal renal function tests which were noted on the routine prenatal check at 32 weeks of gestation delivered normally at 37 weeks. The daughter of patient had seizure when she was 6 years old and was diagnosed as polycystic kidney disease by abdorninal computed tomography. This case developed sporadic form of disease without familial history but, the daughter of patient might inherited by autosomal dominant form. The patient's clinical feature was characterized by history of epilepsy, painless abdominal mass due to polycystic kidney disease, abnormal renal function, skin abnormalites including angiofibroma and shagreen patch. Abdominal computed tomography demonstrated numerous variable sized cysts throughout both kidney. In second case, the patient was a 32-year-female patient complaining of 5kg weight gain, abdominal distension due to palpable masses. Her clinical feature was characterized by bilateral huge renal angiomyolipoma with normal renal function and skin abnormality such as erythematous papule on the face. Abd CT and MRI revealed huge angiomyolipoma of about 15cm×18.5cm×30cm and 14.5cm×18cm×30cm res- pectively. We presented the two cases with brief review of the literatures.
권영석 ( Young Seok Kwon ),문성훈 ( Sung Hoon Moon ),강호석 ( Ho Suk Kang ),임현 ( Hyun Lim ),최난영 ( Nan Young Choi ),김순영 ( Soon Young Kim ),강동훈 ( Dong Hun Kang ),김종혁 ( Jong Hyeok Kim ) 대한췌담도학회 2015 대한췌담도학회지 Vol.20 No.2
자가면역췌장염과 췌장암의 감별진단은 유사한 임상증상들과 영상검사소견을 보일 수 있기 때문에 종종 어렵다. 혈청 IgG4는 자가면역췌장염과 췌장암의 감별에 중요한 인자이다. 췌장암 환자에서도 약 10%에서는 혈청 IgG4가 상승할 수 있으나, 대부분 정상 상한의 2배 이내이다. 그래서 저자들은 자가면역췌장염과 감별이 어려웠던 혈청 IgG4가 정상 상한의 6배 이상으로 상승된 췌장암 1예를 경험하였기에 문헌 고찰과 함께 보고하는 바이다. Differential diagnosis between autoimmune pancreatitis (AIP) and pancreatic cancer is often difficult due to similar clinical manifestations and radiological findings. Serum immunoglobulin G4 (IgG4) is a marker to differentiate AIP from pancreatic cancer. Although serum IgG4 can be elevated in 10% of patients with pancreatic cancer, most of serum IgG4 elevation in pancreatic cancer is limited within two times of upper normal limit. Herein, we report a case of pancreatic cancer with markedly elevated serum IgG4 over six times of upper normal limit that needed steroid trial to differentiate from AIP. Korean J Pancreatobiliary 2015;20(2):78-82
김영규(Young-Kyu Kim),이종훈(Jong-Hun Lee),곽지훈(Ji-Hoon Kwak),문성훈(Sung-Hoon Moon) 대한정형외과학회 2008 대한정형외과학회지 Vol.43 No.3
목적: 불응성 외 상과염의 치료로 개방적 유리술과 관절경적 유리술을 시행한 예를 분석하여 임상적 결과를 비교하고자 하였다. 대상 및 방법: 34예를 대상으로 평균 16개월 추시하였다. 21예에서 개방적 유리술, 13예에서 관절경적 유리술을 시행하였으며 개방적 유리술을 시행한 예 중 7예에서는 관절경 검사를 먼저 시행하였다. 단 요 수근 신근의 관절내, 외측 병변을 비교하였으며 치료 결과는 시각 상사 척도(Visual Analog Scale)를 이용하여 동통을 평가하였고 기능 평가는 Nirschl과 Pettrone의 평가 방법으로 판정하였다. 결과: 관절경적 소견은 20예 중 6예(30%)에서 거의 정상 관절막을 보였고, 단 요 수근 신근에 세동을 보인 예가 6예(30%), 선상 파열이 4예(20%), 견열 파열이 4예(20%)에서 관찰되었다. 관절경 소견상 거의 정상의 관절막을 가졌으나 개방적 유리술 시 점액성 변성의 병변이 관찰된 예는 5예 중 3예 있었다. 결과는 개방적 유리술의 경우 86%, 관절경적 유리술의 경우 85%에서 만족스러운 결과를 보였다. 결론: 수근 신근 기시부의 관절내, 외의 육안적 소견은 여러 형태를 보였다. 두 술식의 임상적 결과는 유의한 차이없이 만족스러운 결과를 나타내어 관절경적 유리술도 불응성 외 상과염의 치료에 유용한 방법이라 사료된다. Purpose: To compare clinical outcomes when using open or arthroscopic release for recalcitrantlateral epicondylitis. Materials and Methods: A total of 34 cases were followed up for an average of 16 months. Open release was performed in 21, and arthroscopic release in 13. In the open release group, arthroscopic examination was performed first in 7. Intraarticular and extraarticular lesions of the extensor tendon were compared. Pain was evaluated using the Visual Analog Scale, and function was evaluated using the assessment of Nirschl and Pettrone. Results: In arthroscopic findings, 6 out of 20 cases were nearly normal, 6 showed fraying, 4 a linear tear, and 4 avulsion. Some (3 of 5) cases with nearly normal arthroscopic findings had mucinoid degeneration detected during the open procedure. Overall, 86% of open release and 85% of arthroscopic release showed satisfactory results. Conclusion: The extraarticular and intraarticular surfaces of the extensor origin had diverse appearances, and both procedures showed satisfactory results. Therefore, arthroscopic release is a useful treatment option for recalcitrant lateral epicondylitis.