1.A Case of Partial Renal Infarction due to Trauma.
Kil Sung KWON ; In Chul CHANG ; Tai Kyung KIM ; Su Kil LIM
Korean Journal of Urology 1982;23(8):1202-1204
One case of renal infarction due to trauma in a 26 years old male patient, which was treated with partial nephrectomy, was presented with the brief review of literature.
Adult
;
Humans
;
Infarction*
;
Male
;
Nephrectomy
2.Effect of Cortisone and X-ray Irradiation on Mast Cells of the Adrenalectomized Albinor Rats.
Yung Keun OH ; Soo Yun PAK ; Tai Su KWON ; Kum Duck CHOI
Yonsei Medical Journal 1964;5(1):6-12
The effects of cortisone administration and whole body irradiation by X-ray upon mesenteric mast cells of intact and adrenalectomized albino rats were studied. In intact rats, the administration of cortisone (50mg./kg) and whole body irradiation by X-ray (800r) caused severe degranulation and disruption of mesenteric mast cells within 24 hours. However their degranulation and disrupting effects upon mesenteric mast cells were markedly inhibited after the removal of the adrenal gland. Although the adrenalectomy alone hardly caused these morphological changes of mesenteric mast cells of the albino rats. According to this experiment it is fairly clear that the effects of cortisone and whole body X-ray irradiation inducing degranulation and disruption of mesenteric mast cells of the albino rats, were not direct phenomena but they indirectly affected the mesenteric mast cells through some special mechanism mediated by the adrenal gland.
4.Expression of human papillomavirs 18 capsid protein L2 in insect cells.
Byung Tae KANG ; Seung Won JIN ; Eun Kyung YANG ; Dur Han KWON ; Soon Hee PARK ; C Young KANG ; Wang Don YOO ; Hyun Su KIM ; In Seong CHOE ; Tai Wha CHUNG
Journal of the Korean Society of Virology 1993;23(2):233-238
No abstract available.
Capsid Proteins*
;
Capsid*
;
Humans*
;
Insects*
5.Differential Effects of Typical and Atypical Antipsychotics on MK- 801-induced EEG Changes in Rats.
Jee Sook KWON ; Ki Min KIM ; Su Min CHANG ; Choong Young KIM ; Tai Ho CHUNG ; Byung Ju CHOI ; Maan Gee LEE
The Korean Journal of Physiology and Pharmacology 2005;9(1):17-22
We examined whether the abnormal EEG state by NMDA receptor blocker MK-801 can be reversed by typical and atypical antipsychotics differentially by comparing their spectral profiles after drug treatment in rats. The spectral profiles produced by typical antipsychotics chlorpromazine (5 mg/kg, i.p.) and haloperidol (0.5 mg/kg, i.p.) were differ from that by atypical antipsychotic clozapine (5 mg/kg, i.p.) in the rats treated with or without MK-801 treatment (0.2 mg/kg, i.p.) which produce behavioral abnormalities like hyperlocomotion and stereotypy. The dissimilarity between the states produced by antipsychotics and the control state was examined with the distance of the location of the canonical variables calculated by stepwise discriminant analysis with the relative band powers as input variables. Although clozapine produced more different state from normal state than typical antipsychotics, clozapine could reverse the abnormal schizophrenic state induced by MK-801 to the state closer to the normal state than the typical antipsychotics. The results suggest that atypical anesthetic can reverse the abnormal schizophrenic state with negative symptom to the normal state better than typical antipsychotic. The results indicate that the multivariate discriminant analysis using the spectral parameters can help differentiate the antipsychotics with different actions.
Animals
;
Antipsychotic Agents*
;
Chlorpromazine
;
Clozapine
;
Dizocilpine Maleate
;
Electroencephalography*
;
Haloperidol
;
N-Methylaspartate
;
Rats*
;
Schizophrenia
6.Clinical Trends in Acute Rheumatic Fever in Korean Children: Mailed Questionnaire Survey from 1988 to 1997(Compared with 1978-1987).
Hyeon Ho KANG ; Sung Ho CHA ; Kyong Su LEE ; Sang Bum LEE ; Tae Chan KWON ; Young Chang TOCKGO ; Chang Sung SON ; Jin A SON ; Hee Ju PARK ; Yong Soo YUN ; Jung Yun CHOI ; Chang Hwi KIM ; Chul Ho KIM ; Tai Ju HWANG ; Jae Sook MA ; Chan Uhng JOO ; Nam Su KIM
Journal of the Korean Pediatric Society 1999;42(10):1381-1391
PURPOSE: The purpose of this study was to assess the frequency of acute rheumatic fever(ARF) among children in Korea and to describe trends in its clinical characteristics compared to data from a previous study(1978-1987). METHODS: A mailed questionnaire survey sent to the pediatric departments of 13 general hospitals in Korea requested the total number of patients with ARF and its clinical manifestations from Jan. 1988 to Dec. 1997. These data were compared with the data from a previous study (1978-1987) to evaluate the clinical trends in occurrence and clinical manifestations of ARF during the last 20 years in Korea. RESULTS: The average number of patients with ARF for the 10-year period(1988-1997) was 0.74 per 1,000 annual pediatric inward patients. There was a significant decrease in incidence during the study period. There were 115 male and 85 female patients with ARF, and 97.5% of total patients were 6 to 15 years old. 126 out of 200 patients(63.0%) had a history of preceding upper respiratory infection(URI). The percentage of major manifestations were as follows; carditis(66.5%),polyarthritis(54.0%), erythema marginatum(12.0%), chorea(7.5%) and subcutaneous nodule (6.0%). Clinical findings of carditiswere cardiac murmur(91.0%), cardiomegaly in chest PA(34.6%), congestive heart failure(15.8%). The electrocardiographic findings were PR interval prolongation (37.6%), right ventricular hypertrophy (RVH) and left ventricular hypertrophy(LVH)(15.8%), QT interval prolongation(13.5%). Doppler echocardiographic valvular lesions were mitral insufficiency(96.2 %), aortic insufficiency(39.8%). Minor and other clinical manifestations were fever(69.0%), arthralgia (56.5%), sore throat(28.5%). CONCLUSION: There was a steady decrease in the number of patients with ARF during the study period from 1988 to 1997. A sudden decrease in number of patients with ARF between the two study periods is likely due to patients with valvular heart disease, possibility of double registration, and wide spread use of echocardiography for accurate diagnosis.
Adolescent
;
Arthralgia
;
Cardiomegaly
;
Child*
;
Diagnosis
;
Echocardiography
;
Electrocardiography
;
Erythema
;
Estrogens, Conjugated (USP)
;
Female
;
Heart
;
Heart Valve Diseases
;
Hospitals, General
;
Humans
;
Hypertrophy, Right Ventricular
;
Incidence
;
Korea
;
Male
;
Postal Service*
;
Surveys and Questionnaires*
;
Rheumatic Fever*
;
Thorax
7.A Case of Left Ventricular Noncompaction Accompanying Fasciculo-Ventricular Accessory Pathway and Atrial Flutter.
Sun Mie YIM ; Sung Won JANG ; Hyun Ji CHUN ; Su Jung KIM ; Kyu Young CHOI ; Beom June KWON ; Dong Bin KIM ; Eun Joo CHO ; Man Young LEE ; Tai Ho RHO ; Jae Hyung KIM
Korean Circulation Journal 2012;42(10):705-708
Left ventricular hypertrabeculation/noncompaction (LVHT) is an uncommon type of genetic cardiomyopathy characterized by trabeculations and recesses within the ventricular myocardium. LVHT is associated with diastolic or systolic dysfunction, thromboembolic complications, and arrhythmias, including atrial fibrillation, ventricular arrhythmias, atrioventricular block and Wolff-Parkinson-White syndrome. Herein, we describe a patient who presented with heart failure and wide-complex tachycardia. Echocardiography showed LVHT accompanied with severe mitral regurgitation. The electrophysiologic study revealed a fasciculo-ventricular accessory pathway and atrial flutter (AFL). The AFL was successfully treated with catheter ablation.
Arrhythmias, Cardiac
;
Atrial Fibrillation
;
Atrial Flutter
;
Atrioventricular Block
;
Cardiomyopathies
;
Catheter Ablation
;
Echocardiography
;
Heart Failure
;
Humans
;
Isolated Noncompaction of the Ventricular Myocardium
;
Mitral Valve Insufficiency
;
Myocardium
;
Pre-Excitation, Mahaim-Type
;
Tachycardia
;
Wolff-Parkinson-White Syndrome
8.Safety and Temporal Pattern of the Lymphocyte Count During Fingolimod Therapy in Patients With Multiple Sclerosis: Real-World Korean Experience
So-Young HUH ; Su-Hyun KIM ; Ki Hoon KIM ; Young Nam KWON ; Sung-Min KIM ; Seung Woo KIM ; Ha Young SHIN ; Yeon Hak CHUNG ; Ju-Hong MIN ; Jungmin SO ; Young-Min LIM ; Kwang-Kuk KIM ; Nam-Hee KIM ; Tai-Seung NAM ; Sa-Yoon KANG ; Jeeyoung OH ; Seong-il OH ; Eunhee SOHN ; Ho Jin KIM
Journal of Clinical Neurology 2022;18(6):663-670
Background:
and Purpose Fingolimod (FTY) inhibits lymphocyte egress from lymphoid organs to cause lymphopenia, but the clinical implications of FTY-induced lymphopenia are not fully understood. We aimed to determine the frequency and severity of lymphopenia during FTY treatment among Korean patients with multiple sclerosis (MS), and its association with infections.
Methods:
We retrospectively reviewed the medical records of patients with MS treated using FTY from 12 referral centers in South Korea between March 2013 and June 2021. Patients were classified according to their nadir absolute lymphocyte count (ALC) during treatment:grade 1, 800–999/μL; grade 2, 500–799/μL; grade 3, 200–499/μL; and grade 4, <200/μL.
Results:
FTY treatment was administered to 69 patients with a median duration of 18 months (range=1–169 months), with 11 patients being treated for ≥7 years. During FTY treatment, mean ALCs were reduced after the first month (653.0±268.9/μL, mean±standard deviation) (p<0.0001) and remained low during treatment lasting up to 84 months. During follow-up, 41 (59.4%) and 7 (10.1%) patients developed grade-3 and grade-4 lymphopenia, respectively.No significant difference was found in age at FTY initiation, sex, baseline ALC, body mass index, or prior disease-modifying treatment between patients with and without grade-4 lymphopenia. Infections were observed in 11 (15.9%) patients, and the frequencies of patients with and without grade-4 lymphopenia were similar.
Conclusions
FTY treatment induced grade-4 lymphopenia in 10% of South Korean patients with MS, but did not appear to be associated with an increased infection risk.
9.Prevalence of Anti-Ganglioside Antibodies and Their Clinical Correlates with Guillain-Barre Syndrome in Korea: A Nationwide Multicenter Study.
Jong Kuk KIM ; Jong Seok BAE ; Dae Seong KIM ; Susumu KUSUNOKI ; Jong Eun KIM ; Ji Soo KIM ; Young Eun PARK ; Ki Jong PARK ; Hyun Seok SONG ; Sun Young KIM ; Jeong Geun LIM ; Nam Hee KIM ; Bum Chun SUH ; Tai Seung NAM ; Min Su PARK ; Young Chul CHOI ; Eun Hee SOHN ; Sang Jun NA ; So Young HUH ; Ohyun KWON ; Su Yun LEE ; Sung Hoon LEE ; Sun Young OH ; Seong Hae JEONG ; Tae Kyeong LEE ; Dong Uk KIM
Journal of Clinical Neurology 2014;10(2):94-100
BACKGROUND AND PURPOSE: No previous studies have investigated the relationship between various anti-ganglioside antibodies and the clinical characteristics of Guillain-Barre syndrome (GBS) in Korea. The aim of this study was to determine the prevalence and types of anti-ganglioside antibodies in Korean GBS patients, and to identify their clinical significance. METHODS: Serum was collected from patients during the acute phase of GBS at 20 university-based hospitals in Korea. The clinical and laboratory findings were reviewed and compared with the detected types of anti-ganglioside antibody. RESULTS: Among 119 patients, 60 were positive for immunoglobulin G (IgG) or immunoglobulin M antibodies against any type of ganglioside (50%). The most frequent type was IgG anti-GM1 antibody (47%), followed by IgG anti-GT1a (38%), IgG anti-GD1a (25%), and IgG anti-GQ1b (8%) antibodies. Anti-GM1-antibody positivity was strongly correlated with the presence of preceding gastrointestinal infection, absence of sensory symptoms or signs, and absence of cranial nerve involvement. Patients with anti-GD1a antibody were younger, predominantly male, and had more facial nerve involvement than the antibody-negative group. Anti-GT1a-antibody positivity was more frequently associated with bulbar weakness and was highly associated with ophthalmoplegia when coupled with the coexisting anti-GQ1b antibody. Despite the presence of clinical features of acute motor axonal neuropathy (AMAN), 68% of anti-GM1- or anti-GD1a-antibody-positive cases of GBS were diagnosed with acute inflammatory demyelinating polyradiculoneuropathy (AIDP) by a single electrophysiological study. CONCLUSIONS: Anti-ganglioside antibodies were frequently found in the serum of Korean GBS patients, and each antibody was correlated strongly with the various clinical manifestations. Nevertheless, without an anti-ganglioside antibody assay, in Korea AMAN is frequently misdiagnosed as AIDP by single electrophysiological studies.
Amantadine
;
Antibodies*
;
Axons
;
Cranial Nerves
;
Facial Nerve
;
Guillain-Barre Syndrome*
;
Humans
;
Immunoglobulin G
;
Immunoglobulin M
;
Korea
;
Male
;
Ophthalmoplegia
;
Prevalence*