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A peripheral tremor associated with intractable pain after traffic accident: case report
홍주철,김성호 영남대학교 의과대학 2009 Yeungnam University Journal of Medicine Vol.26 No.1
There are debates about whether peripherally induced movement disorders exist. We report a case of upper limb tremor induced by peripheral nerve injury. A 25-year-old male patient presented with pain and tremor of the left upper extremity, 2 days after a car accident. Magnetic resonance images of the brain and cervical spine were normal. His past medical history was unremarkable and there were no family members with symptoms of movement disorders. He suffered from an aggravating tremor for about 10 minutes, four to six times a day. We treated the patient with medication, epidural infusion, cervical nerve root block and trigger point injection of the trapezius muscle. The pain subsided 50% and the incidence of tremor attacks was reduced to once or twice a day. The role of peripheral trauma in the genesis of movement disorders has not been generally accepted. It is unclear whether peripheral trauma can induce dystonia and other movement disorders. It has been proposed that peripheral trauma can alter sensory input and induce cortical and subcortical reorganization that generates a movement disorder. Some studies provide evidence for central reorganization following peripheral injury.
홍장수,박주철,노준량,김종환,서경필,이영균,Hong, Jang Soo,Park, Joo Chul,Rho, Joon Ryang,Kim, Chong Whan,Suh, Kyung Phil,Lee, Yung-Kyoon 대한흉부심장혈관외과학회 1976 Journal of Chest Surgery (J Chest Surg) Vol.9 No.2
Truncus arteriosus is a rare and highly lethal cardiac anomaly characterized by a single arterial trunk emerging from the heart and supplying the coronary, systemic, and pulmonary circulations, The first successful correction of truncus arteriosus was reported by McGoon et al. in 1968 and was based on experimental work reported by Rastelli et al. in 1967 in which a conduit consisting of a homograft of the ascending aorta and aortic valve was used to establish continuity between the right ventricle and the pulmonary arteries, Modification of this procedure using a Dacron tube valved with porcine xenograft instead of a homograft have resulted in the current definite treatment for truncus arteriosus. This report describes an 3 years and 4 months old boy with heart failure from type I truncus arteriosus who was diagnosed as the V. S. D. with pulmonary hypertension preoperatively and underwent corrective surgery employing the Rastelli procedure using a Dacron conduit valved with canine xenograft, but died due to massive bleeding from the anastomosis sites in operating room.
Galantamine 사용 후 발생한 QT간격의 연장 1예
박주철,김병석,박성민,박일우,홍영미,정준훈,차태준 고신대학교 의과대학 2011 고신대학교 의과대학 학술지 Vol.26 No.2
Among the Acetylcholinesterase inhibitors as used for Alzheimer's disease treatment, Galantamine has been recently developed and widely used owing to proven its clinical efficacy and safety. However, it has reported that prolonged QT interval, which can lead to ventricular arrythimias such as Torsade de points, has developed in Galantamine-treated patients. A 74-year-old female Alzheimer's patient been treated with galantamine for 8 months visited the hospital complaining about frequent dizziness. ECG monitor was performed promptly, it was informed that the prolonged QTc interval was increased 450 ms to 486 ms. So, we made her stop taking the galantamine, and after that QTc interval has normalized to 406 ms. In this article, we reported the first case on prolonged QT interval associated with galantamine in Korea.
Burkholderia pseudomallei에 의한 전립선 농양
홍영미 ( Young Mi Hong ),김병석 ( Byung Seok Kim ),박성민 ( Seong Min Park ),박일우 ( Il Woo Park ),박주철 ( Ju Chul Park ),이병희 ( Byung Hee Lee ),조현명 ( Hyun Myung Cho ) 대한내과학회 2011 대한내과학회지 Vol.81 No.4
Melioidosis is an infectious disease caused by the Gram-negative bacillus, Burkholderia pseudomallei. It is endemic in Southeast Asia and northern Australia, where B. pseudomallei is a soil saprophyte and invades the host through inoculation, inhalation or ingestion. It infects mostly adults with predisposing conditions, mainly diabetes mellitus. The lung is the most commonly affected organ, presenting with either cough or fever resulting from a primary spread. Also, seeding and abscess formation can arise in any organ. However, prostatic abscess due to melioidosis is uncommon. We report a case of pneumonia, and prostate and scrotal abscesses due to Burkholderia pseudomallei, in a 48-year-old man with diabetes mellitus who had a history of working in Malaysia. This is the first report of genitourinary infection of melioidosis in Korea. (Korean J Med 2011;81:526-532)
홍장수,박주철,김종환,Hong, Jang-Soo,Park, Ju-Cheol,Kim, Jong-Hwan 대한흉부심장혈관외과학회 1977 Journal of Chest Surgery (J Chest Surg) Vol.10 No.1
Congenital lobar emphysema is one of the many causes of the respiratory distress syndrome in infant and an unusual condition barely mentioned before 1949, and only 166 cases were reported till 1967 in English literature This report describes a one-month-old boy who had a congenital middle lobar emphysema. The middle lobectomy was the operation for this case with complete cure.
Clinicoepidemiological Features of Asymptomatic Moyamoya Disease in Adult Patients
양제열,홍주철,오창완,권오기,황교준,김정은,강현승,조원상,김택균,문종언,안성열,김준학,방재승 대한뇌혈관외과학회 2014 Journal of Cerebrovascular and Endovascular Neuros Vol.16 No.3
Objective : The aim of this study was to document the natural course ofasymptomatic adult moyamoya disease (MMD) and the factors related todisease progression to aid in treatment decisions. Materials and Methods : Among 459 adult MMD patients (aged ≥ 20 years),42 patients were included in this retrospective cohort study. Clinical records ofadult asymptomatic MMD patients (n = 42) and follow-up data from September2013 were reviewed to determine the factors related to disease progression. Results : The mean age of patients at the time of diagnosis was 41.2years (range, 23-64 years), and the mean follow-up period was 37.3 months(range, 7.4-108.7 months). Of the 42 patients and 75 hemispheres, therewere 12 patients (28.6%) and 13 hemispheres (17.3%) with disease progression. There were four hemispheres (5.3%) with symptomatic progression (threehemorrhage, one transient ischemic attack) and nine hemispheres (12.0%)with asymptomatic radiographic progression. There were no relationshipswith sex, diabetes, hypertension, thyroid disease, family history of MMD,or family history of stroke. However, reduced initial cerebrovascular reservecapacity was observed in seven hemispheres (9.3%) in patients withdisease progression. A relationship was found between disease progressionand initial cerebrovascular reserve capacity (p = 0.05). None of the patientsunderwent bypass surgery during the follow-up period. Conclusion : It appears that asymptomatic adult MMD is not a permanentstable disease. In particular, reduced cerebrovascular reserve capacityis an indication of MMD progression, so close regular observation is needed.
건강한 성인에서 발생한 Gemella morbillorum에 의한 간농양 1예
박일우,박성민,박주철,김병석,홍영미,이준상,임주견 대한감염학회 2011 Infection and Chemotherapy Vol.43 No.4
Gemella morbillorum is a normal flora of the oral cavity, upper respiratory tract, gastrointestinal tract, or genitourinary system. Human infection cause by G. morbillorum is very rare. Known predisposing conditions are intravenous drug abuse, alcoholism, cardiovascular disease, chronic obstructive pulmonary disease, diabetes, renal disease and poor oral hygiene. Most reported cases are infective endocarditis and vasculitis. We experienced a case of liver abscess by G. morbillorum in a healthy young woman, who was treated successfully with antibiotics and drainage. We report this case along with a literature review.
심첨부 비후형 심근증에서 C,S 단백이 동반 결핍된 폐동맥 색전증 1례
박성민,김병석,홍영미,박일우,박주철,정준훈,이재우 고신대학교 의과대학 2011 고신대학교 의과대학 학술지 Vol.26 No.1
Pulmonary embolism is caused by various conditions including genetic and acquired factors, and among them, C and S protein deficiency are known as a cause of pulmonary embolism although their incidences are low. Apical hypertrophic cardiomyopathy is known as a subtype of hypertrophic cardiomyopathies which was reported to be a cause of diastolic heart failure or thromboembolism by activating coagulation system, and this may have an effect on developing pulmonary embolism. We report this since we experienced a case of both C and S protein deficiencies in a patient with apical hypertrophic cardiomyopathy who was diagnosed as pulmonary embolism and has been examined to find the cause of the disease.