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흡입용 스테로이드인 Budesonide 6주 치료가 기관지 천식환자의 기관지 과민반응과 부신피질기능에 미치는 영향
김관형 ( Kwan Hyong Kim ),오용석 ( Yong Seok Oh ),김치홍 ( Chi Hong Kim ),권순석 ( Soon Seog Kwon ),김영균 ( Young Kyoon Kim ),한기돈 ( Ki Don Han ),문화식 ( Hwa Sik Moon ),송정섭 ( Jeong Sup Song ),박성학 ( Sung Hak Park ) 대한결핵 및 호흡기학회 1992 Tuberculosis and Respiratory Diseases Vol.39 No.3
증례보고 : 전신마취하 제왕절개술 중 발생된 고도 방실 차단
이해진 ( Hae Jin Lee ),전진영 ( Jin Young Chon ),오용석 ( Yong Seog Oh ),김나현 ( Na Hyun Kim ) 대한마취과학회 2006 Korean Journal of Anesthesiology Vol.51 No.5
This report is presented in which an asymptomatic parturient with Mobitz I second degree heart block developed high grade heart block during cesarean section under general anesthesia with enflurane. Progression of the block might be associated with vagal reflex. The event in this case suggests that the patients with pre-existing heart block may be a risk factor for development of high grade atrioventricular block during general anesthesia and surgery. (Korean J Anesthesiol 2006; 51: 641~3)
증례 : 순환기 ; 좌회선지 원위부에서 우관상동맥이 기원하는 단일 관상동맥 기형 1예
박하욱 ( Ha Wook Park ),류시영 ( Si Young You ),윤재승 ( Jae Seung Yun ),이해미 ( Hae Mi Lee ),이수연 ( Soo Yeon Lee ),정욱성 ( Wook Sung Chung ),오용석 ( Yong Seog Oh ) 대한내과학회 2011 대한내과학회지 Vol.80 No.2S
선천성 심장이상을 동반하지 않은 단일 관상동맥 기형은 매우 드물고, 특히 우관상동맥이 좌회선지의 원위부에서 기시하는 경우는 현재까지 국내에서 1예, 전 세계적으로는 18예에서만 보고되었다. 단일 관상동맥 기형은 분류에 따라 급성 심장사를 일으킬 수 있는 경우가 있어 임상적으로 중요한 의의를 갖지만, 환자의 평가 및 치료에는 정확한 지침이 없는 실정이다. 저자들은 미세혈관 협심증으로 진단된 좌회선지 원위부에서 기원하는 우관상동맥을 보이는 단일 관상동맥 기형 1예를 경험하였기에 문헌고찰과 함께 보고하는 바이다. Single coronary artery (SCA) is a rare congenital anomaly and commonly associated with other congenital cardiac malformations. Some subgroups of SCA can lead to angina pectoris, acute myocardial infarction, or even sudden cardiac death in the absence of atherosclerosis. An anomalous origin of the right coronary artery, arising from the distal portion of the left circumflex artery, has previously been reported in a few cases. In this article, we report a case of a right coronary artery arising from the distal portion of the left circumflex artery with no other cardiac congenital anomaly. (Korean J Med 2011;80:S172-S177)
간문맥혈전을 동반한 간암에서 경동맥화학색전 요법후 방사선조사 및 온열요법의 효과
최규용,김기태,배시현,김부성,박두호,최종영,박영민,오용석,윤승규,김창섭,방승호,김희열,윤세철 대한내과학회 1994 대한내과학회지 Vol.47 No.4
Primary Hepatocellular carcinoma (HCC) is well recognized as one of the most malignant tumors with a dismal prognosis Although surgical resection is effective in small solitary HCC, only 10%. of tumors are resectable. As a result, most HCC patients receive palliative therapy. Many efforts have been made in the treatment of the advanced HCC; systemic chemotherapy, transcatheter arterial chemo-embolization (TACE), percutaneous ethanol injection therapy (PEIT). The prognosis of HCC with main portal vein tumor thrombus is very poor due to limitation of treatment modality and poor results of treatment. Radiation therapy is known to be effective in the treatment of unresectable HCC and even in the case of portal vein tumor thrombus. Now we report three cases of advanced HCC with portal vein tumor thrombus or inferior vena cava thrombus that was treated with combined radiotherapy and hyperthermia after TACE.
박종원,강문원,신완식,김춘추,오용석,유진홍,김동집,김양리,한치화 대한내과학회 1995 대한내과학회지 Vol.49 No.4
Typhlitis is a life-threatening disease of bowel, mainly ileum or cecum, complicated in the immunocompromised hosts. Recently we experienced four cases of typhlitis in leukemic patients following cytotoxic chemotherapy. All the patients were diagnosed as acute myelogenous leukemia and received cytotoxic chemotherapy followed by granulocytopenia. They mainly showed fever, abdominal pain, and diarrhea. In one case, he suffered from intestinal obstruction. Abdominal CT showed diffuse thickening of ileocecal region or ascending colon. Stool culture revealed Staphylococcus aureus in two cases and Entercoccus species in one case. Staphylococcus aureus was isolated from blood culture in one case. They were managed medically and three out of four cases survived.
양진모,노희정,윤영연,오용석,변재영,정해억,김창섭,홍관수,안석주,최상욱 대한감염학회 1994 감염 Vol.26 No.2
저자들은 50세의 남자에서 수술후 발생한 양측성 후복막강 농양에 대해 경피적 배농술로 성공적으로 치료한 1예를 문헌 고찰과 함께 보고하는 바이다. Retroperitoneal abscesses are complicated serious surgical infections marked by an insidious, occult process leading to considerable mortality and morbidity. Knowledge of the anatomy of the retroperitoneal spaces as well as an increased awareness of the symptoms, physical findings, and causes of these abscesses are the keys to prompt and efficient therapy. Recently percutaneous guided catheter drainage has changed the traditional surgical therapeutic approach to this disease in the majority of cases. We report a case of postoperative complicated bilateral retroperitoneal abscess successfully treated with percutaneous guided catheter drainage combined with medical control.
강성구,이광우,손호영,강무일,윤건호,손현식,유순집,홍관수,오용석 대한내분비학회 1992 Endocrinology and metabolism Vol.7 No.2
Male pseudohermaphroditism is a sexual differentiation disorder in which the affected patient has gonads that are testes, but the genital ducts or external genitalia are not completely masculinized due to deficient testosterone secretion as a consequence of (1) a defect in testicular differentiation, (2) failure of secretion of testosterone or m llerian duct inhibitory factor, (3) failure of target tissue response to testosterone or dihydrotestosterone, and (4) failure of conversion of testosterone to dihydrotestosterone. Of these, a defect in 17 -hydroxylation of pregnenolone precludes formation of corisol and sex steroids in man, which results in elevated plasma concentrations of deoxycorticosterone (DOC) and corticosterone (B), hypertension, hypokalemia, and suppression of renin and aldosterone production. We experienced a case of 17 -hydroxylase deficiency in a 21-year-old phenotypically female who was admitted to our hospital due to primary amenorrhea and hypertension. The characteristic findings were decreased serum cortisol level, hypokalemia, metabolic alkalosis, increased urinary metabolite of DOC. The sex chomosomal analysis showed male XY. The patient was diagnosed as male pseudohermaphroditism due to 17 -hydroxylase deficiency, so we report a case with the review of the literature. (J Kor Soc Endocrinol 7:153~159, 1992)