1.Changes in Blood Superoxide Dismutase Activities after Alcohol Withdrawal.
Jin Sook CHEON ; Kyu Cheon LEE ; Byoung Hoon OH
Journal of the Korean Society of Biological Psychiatry 1999;6(2):219-226
OBJECTIVES: The aims of this study were to evaluate changes in plasma superoxide dismutase(SOD) activities in alcohol depedence, to fine out variables to influence on the SOD activities, and finally to identify the correlation of SOD activities with the alcohol-associated cognitive disorders. METHODS: For 24 male alcoholics and 21 healthy male controls, plasma SOD activities were measured by spectrophotometry on 1-2 wks after alcohol withdrawal. Structured interviews and laboratory tests were also performed. RESULTS: 1) Upon comparing SOD activities between controls and alcoholics, the SOD activities were significantly(p<0.01) lower in alcoholics(0.308+/-0.140 units/mL) than in healthy controls(0.313+/-0.086 units/mL). 2) Upon comparing SOD activities according to the presence of alcohol-related cognitive disorders, the SOD activities were significantly(p<0.05) lower in alcoholics with cognitive disorders(0.247+/-0.049 units/mL) than in alcoholics without cognitive disorders(0.317+/-0.148 units/mL). 3) Upon comparing SOD activities according to the presence of alcoholic polyneuropathy or alcohol withdrawal seizure, the SOD activities showed no significant differences between alcoholics with polyneuropathy or epilepsy and those without. 4) Upon analyzing variables influencing on the SOD activities in alcoholics, the SOD activities had the negative correlation with hemoglobin(gamma=-0.433) and severity of alcohol withdrawal symptoms(gamma=-0.375). 5) Upon comparing variables according to the presence of alcohol-related cognitive disorders, the occurrence of alcoholic polyneuropathy(p<0.05) and blood phosphorus concentrations(p<0.01) were significantly higher in alcoholics with cognitive disorders than those without. 6) Upon analyzing an association between SOD activities and variables in alcoholics with cognitive disorders, the SOD activities were positively correlated with the onset age(gamma=0.995), and negatively correlated with the severity of alcohol withdrawal symptoms(gamma=-0.996). CONCLUSIONS: Lower SOD activities in alcohol dependence suggested alcohol-associated cognitive disorders and alcohol withdrawal symptoms might be caused by oxidative stress.
Alcohol Withdrawal Seizures
;
Alcoholic Neuropathy
;
Alcoholics
;
Alcoholism
;
Epilepsy
;
Humans
;
Male
;
Oxidative Stress
;
Phosphorus
;
Plasma
;
Polyneuropathies
;
Spectrophotometry
;
Substance Withdrawal Syndrome
;
Superoxide Dismutase*
;
Superoxides*
2.Intrasellar arachnoid cyst with endocrine and anxiety manifestations.
Journal of Korean Neuropsychiatric Association 1991;30(5):927-933
No abstract available.
Anxiety*
;
Arachnoid*
3.Comparison of measurements of airway resistance during panting and quiet breathing.
Seon Hee CHEON ; Woo Hyung LEE ; Kee Young LEE ; Se Kyu KIM ; Joon CHANG ; Sung Kyu KIM ; Won Young LEE
Tuberculosis and Respiratory Diseases 1993;40(3):267-273
No abstract available.
Airway Resistance*
;
Respiration*
4.Congenital anomalies of the ribs
Chang Kyu LIM ; Kyung Won LEE ; Jae Cheon BIN ; Byung Chull RHEE
Journal of the Korean Radiological Society 1982;18(3):487-495
Conegenital anomalies of the ribs are common but rarely result in shadow which might be mistaken forpathological lesions. Careful inspection of the bony parts, which should be a routine, will usually be sufficientto avoid mistakes. Authors reviewed 6,921(5,865 male, 1,056 female) chest P-A films in adult (older than 16years), and radiolographic findings of congenital anomalies of the ribs were analized. The result were as follows;1. Congenital anomalies of the ribs were present in 193 patients. The incidence of congenital anomalies of theribs were 2.7% in male, 3.3% in female. 2. Among the 193 cases of congenital rib anomalies, 7 cases(0.1%) ofcervical ribs, 31 cases (0.4%) of underdeveloped ribs, 81 cases (1.2%) of anterior bifurcation, 34 cases (0.5%) ofbroadned ribs, 19 cases (0.3) of complete fusion and 21 cases (0.3%) of pseudathrosis were included. 3. 11.4% ofthe cases were bilateral, and right to left was 4:3 in unilateral involvement. 4. The location of the ribanomalies were as follows; (1) Underdeveloped ribs; 1st rib 31 case (79.5%), 2nd rib 3 cases(7.7%), 4th rib 3cases(7.7%), 5th rib 2 cases(5.1%). (2) Anterior bifurcation; 3rd rib 37 cases. 4th rib 29 cases, 5th rib 12cases, 6th rib 6cases, 2nd rib 2 cases. (3) Broadened ribs; 3rd 17 cases, 4th rib 15 cases, 5th rib 4 cases, 2ndrib 1 case. (4) Complete fusion; 1st-2nd rib 13 cases (68.4%), 5-6th ribs 4 cases (21.0%), 4-5th ribs 1case(5.3%), 6-7 ribs 1case(5.3%). The fusion occur in the posterior portion of 1st-2nd and 4-5th ribs,and in theposterior portion of 5-6th and 6-7ribs. (5) Pseudarthrosis; 1st-2nd and 2nd-3rd ribs, and in the posterior portionof 3-4th, 4-5 and 5-6th ribs. 5. In the cases of anterior bifurcation, the rib bifurcates almost in its anterior2.1-5.0 cm and most common in 3.1-4.0cm. 6. The characteristic radiographic findings in anterior bifurcation wereas follow;
Adult
;
Female
;
Humans
;
Incidence
;
Male
;
Pseudarthrosis
;
Ribs
;
Thorax
5.Assessment of the relationship between pulmonary function test and dyspnea index in patients with bronchial asthma.
Se Kyu KIM ; Seon Hee CHEON ; Joon Ha CHANG ; Won Hong JONG ; Soo CHEIN ; Sung Kyu KIM ; Won Young LEE
Tuberculosis and Respiratory Diseases 1992;39(5):392-399
No abstract available.
Asthma*
;
Dyspnea*
;
Humans
;
Respiratory Function Tests*
6.Extracardiac uptake of thallium-201 during myocardial perfusionimaging with pharmacologic vasodilation.
Chung Il CHOI ; Dong Sik KWAK ; Byung Cheon CHUNG ; Moo Keun PARK ; Jae Tae LEE ; Kyu Bo LEE
Korean Journal of Nuclear Medicine 1992;26(1):65-71
No abstract available.
Vasodilation*
7.Polymorphism of the ACE Gene in Dialysis Patients: Overexpression of DD Genotype in Type 2 Diabetic End-Stage Renal Failure Patients.
Hyeong Cheon PARK ; So Rae CHOI ; Beom Seok KIM ; Tae Hee LEE ; Byung Seung KANG ; Kyu Hyun CHOI ; Ho Yung LEE ; Dae Suk HAN ; Sung Kyu HA
Yonsei Medical Journal 2005;46(6):779-787
The angiotensin-converting enzyme (ACE) gene DD homozygote has been suggested to be a significant risk factor for the progression of diabetic nephropathy. We analyzed clinical parameters and ACE genotype distribution between type 2 diabetic patients at the extremes of renal risk, i.e. an end-stage renal failure (ESRF) group (n = 103, group 1) who were on dialysis therapy due to progression of diabetic nephropathy, and a no progression group (n = 88, group 2) who had maintained normal renal function and normoalbuminuria for more than 15 years. There were no significant differences in age, sex, body mass index, HbA1c level, or lipid profiles between the two groups (p > 0.05). Group 1 had a significantly higher prevalence of hypertension [group 1: 82.5% (85/103) vs. group 2: 50.0% (44/88), p < 0.05] and diabetic retinopathy [group 1: 103/103 (100%) vs. group 2: 28/88 (31.8%), p < 0.05] than group 2. Daily urinary albumin excretion was also higher in group 1 than in group 2 [group 1: 2873 +/- 2176 mg/day vs. 12 +/- 7 g/day, p < 0.05]. The frequencies of the DD, ID, and II genotypes of the ACE gene in group 1 and group 2 were 26.2%, 47.6%, and 26.2%, and 7.9%, 57.9%, and 34.2%, respectively. The ACE genotype frequencies between the two groups were significantly different according to a chi-square test with Bonferroni's correction (p = 0.004). The presence of the DD genotype increased the risk of ESRF 4.286-fold compared to the II genotype [odds ratio 4.286, 95% CI 1.60- 11.42, p = 0.005]. The frequency of the D-allele was higher in both male and female patients in group 1 compared to group 2, but reached statistical significance only in males [male, group 1: 50.8% vs. group 2: 35.0%, p = 0.018, female, group 1: 48.8% vs. group 2: 39.5%, p = 0.231]. This study, although limited by sample size, showed that type 2 diabetic ESRF patients more frequently expressed the DD genotype. These findings may substantiate the previously noted relationship between the ACE DD genotype and the progression of diabetic nephropathy in Korean type 2 diabetic patients.
Renal Dialysis
;
*Polymorphism, Genetic
;
Peptidyl-Dipeptidase A/*genetics/metabolism
;
Middle Aged
;
Male
;
Kidney Failure, Chronic/diagnosis/*genetics
;
Humans
;
Homozygote
;
Gene Frequency
;
Female
;
Diabetic Nephropathies/diagnosis/*genetics
;
Diabetes Mellitus, Type 2/diagnosis/*genetics
;
Aged
8.A Case of Paraneoplastic Limbic Encephalitis Presented with Schizophrenic Symptoms.
Kyu Sik SHIN ; Eun Jin CHEON ; Se Jin LEE
Journal of Korean Neuropsychiatric Association 2015;54(4):596-599
Paraneoplastic limbic encephalitis associated with ovarian teratoma has variable clinical manifestations, including hallucination, abnormal behavior, amnesia, mental change, fever, chorea and dystonia, and often has antibodies to N-methyl-D-aspartate receptor (NMDAR), however cases without tumor or antibodies to NMDAR have also been reported. Here, we describe a 35-year-old female who was initially misdiagnosed as schizophrenia because she presented with acute onset of psychiatric symptoms, including visual hallucination, abnormal behavior, confusion, and memory impairment. Three days after admission, she developed high fever refractory to antibiotics. Brain MRI and examination of cerebrospinal fluid were normal. Computerized tomography of the pelvis showed an ovarian teratoma. The patient showed complete improvement after surgical removal of the ovarian teratoma and steroid therapy. We suggest that physicians should consider the possibility of paraneoplastic limbic encephalitis in patients who present with acute onset of psychiatric symptoms with high fever or movement disorder.
Adult
;
Amnesia
;
Anti-Bacterial Agents
;
Antibodies
;
Brain
;
Cerebrospinal Fluid
;
Chorea
;
Dystonia
;
Female
;
Fever
;
Hallucinations
;
Humans
;
Limbic Encephalitis*
;
Magnetic Resonance Imaging
;
Memory
;
Movement Disorders
;
N-Methylaspartate
;
Pelvis
;
Schizophrenia
;
Teratoma
9.Clinical Analysis of Stereotactic Aspiration and Conservative Management in Spontaneous Thalamic Hematoma.
Cheon Hyun NAM ; Jae Kyu KANG ; Jong Oung DOH ; Chun Dae LEE
Journal of Korean Neurosurgical Society 2001;30(2):156-162
OBJECTIVES: The purpose of this study is to review our experience with spontaneous thalamic hemorrhage. Clinical outcome of patients was brought about by comparing stereotactic aspiration and conservative medical therapy. METHODS: The study consists of seventy-three cases with spontaneous thalamic hemorrhage which were treated from the period of Jan. 1993 to Dec. 1999. Thirty-eighty patients were treated with computed tomography (CT) guided stereotactic aspiration and thirty-five patients were treated conservatively. We compared the factors affecting treatment and the factors are as follows: age and sex, conscious level on admission, hematoma volume, hematoma sites, presence of ventricular penetration. RESULTS: The results in the thirty eight stereotactic aspirated cases for the 6 months from oneset are as follows: good recovery or moderate disability in 43%, severe disability in 32%, vegitative state in 11%, dead in 13% respectively. The clinical result was more favorable in stereotactic aspiration, with 11-30cc hematoma volume, extend to internal capsule of hematoma, poor conscious level on admission than conservative medical therapy. But age and sex, conscious level on admission, presence of ventricular penetration were not influential in the statistical outcome between stereotactic aspiration and conservative medical therapy. CONCLUSION: Treatment modality of spontaneous thalamic hemorrhage is still controversial. But stereotactic aspiration is more recommended for improvement therapeutic results than conservative treatment or open craniotomy in case of 11-30cc hematoma volume, extend to internal capsule of hematoma and poor conscious level on admission.
Craniotomy
;
Hematoma*
;
Hemorrhage
;
Humans
;
Internal Capsule
10.Tailgut Cyst A case report.
Byeong Yul AHN ; Choon Sik JEONG ; Dong Hee LEE ; Chang Sik YU ; Ho Jung LEE ; Moon Kyu LEE ; Jin Cheon KIM
Journal of the Korean Society of Coloproctology 1998;14(3):617-620
Tailgut cyst is a rare congenital lesion in retrorectal space. The clinical significance of tailgut cyst presents its morbidity that occurs in the unrecognized and incompletely treated lesion. A forty four year-old female patient visited with lower abdominal pain during defecation. Preoperative abdominopelvic MRI and endorectal ultrasonography revealed a retrorectal mass suggestive of leiomyoma, dermoid cyst, teratoma, or duplication cyst of rectum. She underwent complete resection of retrorectal mass by transsphincteric approach. The mass was multilocular cyst lined by multiple types of epithelium. It was histologically confirmed as a tailgut cyst. She recovered uneventfully. This report includes the case and a brief review of tailgut cyst.
Abdominal Pain
;
Defecation
;
Dermoid Cyst
;
Epithelium
;
Female
;
Humans
;
Leiomyoma
;
Magnetic Resonance Imaging
;
Rectum
;
Teratoma
;
Ultrasonography