1.Clinical Studies on Congenital Malformation.
Jung Hwan CHOI ; Hun Jong CHUNG ; Chong Ku YUN
Journal of the Korean Pediatric Society 1985;28(4):378-385
No abstract available.
2.Flow Cytometric Analysis of T-cell Subsets in Brain Tumor Patients.
Jung NAM ; Hyoung Ihl KIM ; Jung Chung LEE ; Rae Kil PARK ; Hun Taeg CHUNG
Journal of Korean Neurosurgical Society 1989;18(7-12):977-984
The immunocompetence is important not only to kill the neoplastic cells but also to keep the neoplastic cells from growing further. T lymphocyte is plays the most important role in maintaining the tumor immunity efficiently. T lymphocyte has its specific functions depending in the subset of T lymphocytes. The author analyzed the T lymphocyte subsets in 31 brain tumor patients using anti-CD3, anti-CD4, anti-CD8 monoclonal antibodies and flow cytometry to determine the immunological status of brain tumor patients. All CD3, CD4 and CD8 subsets were reduced in both benign and malignant brain tumor patients but more signigicantly reduced in malignant tumor group. But in benign tumor group, the subtypes of T lymphocytes were not so different from those of normal healthy controls except the pituitary tumor patients, who showed the significant decrease in all the subtypes. In malignant tumor group, each subtype was signigicantly reduced and CD8 subtypes was markedly reduced in metastatic tumor patients, These analyses were considered to have the possibility to be contributable to planning the further immunotherapy and also the possibility to moniter the brain tumor patients clinically.
Antibodies, Monoclonal
;
Brain Neoplasms*
;
Brain*
;
Flow Cytometry
;
Humans
;
Immunocompetence
;
Immunotherapy
;
Lymphocytes
;
Pituitary Neoplasms
;
T-Lymphocyte Subsets*
;
T-Lymphocytes*
3.Malignant Melanoma in the Spinal Cord: Report of a Case.
Hun Hwa JUNG ; Su Hyu KIM ; Sang Sup CHUNG ; Hun Jae LEE
Journal of Korean Neurosurgical Society 1974;3(1):59-62
Malignant melanoma of the spinal cord is a rare tumor 3,8,9,12 The melanomas that originate in the meninges bear a general structural resemblance to those arising elsewhere, but it is questionable whether they ever metastasis outside the central nervous system7. If can be also argued that the primary central nervous system melanoma could actually be a metastasis from an occult primary site in the skin, esophagus, rectum or other sites6. We are reporting a case of malignant melanoma involving the cervical spinal meninges and hard palate.
Central Nervous System
;
Esophagus
;
Melanoma*
;
Meninges
;
Neoplasm Metastasis
;
Palate, Hard
;
Rectum
;
Skin
;
Spinal Cord*
4.Dandy-Walker Cyst Case Report.
Hun Hwa JUNG ; Sang Chul KIM ; Sang Sup CHUNG ; Hun Jae LEE
Journal of Korean Neurosurgical Society 1974;3(1):91-98
In 1921, Dandy discussed the clinical diagnosis and treatment of hydrocephalus secondary to occlusion of the foramina of Magendie and Luschka. In 194, Walker reported a case of congenital atresia of the outlets of the fourth ventricle treated surgically. Since a detailed study of this disease entity by Benda in 1954, the condition has commonly been known by the term, the Dandy-Walker syndrome. In 1968, Raimondi and et al refered this condition as the Dandy-Walker cyst. There is considerable discussion as to the nature of the fundamental embryologic error in this condition, but Denda suggested that atresia of developing fourth ventricular foramina was only a part of the syndrome and not its cause, because in some cases reported, the foramina were found to be patent. These patients. Show characteristic clinical symptoms, signs and radiological findings and should suggest the correct diagnosis. This syndrome was one of the first cause of hydrocephalus to be treated successfully by surgery. We are reporting one case of this cyst encountered recently at Yonsei University Medical Center.
Academic Medical Centers
;
Dandy-Walker Syndrome*
;
Diagnosis
;
Fourth Ventricle
;
Humans
;
Hydrocephalus
5.Dandy-Walker Cyst Case Report.
Hun Hwa JUNG ; Sang Chul KIM ; Sang Sup CHUNG ; Hun Jae LEE
Journal of Korean Neurosurgical Society 1974;3(1):91-98
In 1921, Dandy discussed the clinical diagnosis and treatment of hydrocephalus secondary to occlusion of the foramina of Magendie and Luschka. In 194, Walker reported a case of congenital atresia of the outlets of the fourth ventricle treated surgically. Since a detailed study of this disease entity by Benda in 1954, the condition has commonly been known by the term, the Dandy-Walker syndrome. In 1968, Raimondi and et al refered this condition as the Dandy-Walker cyst. There is considerable discussion as to the nature of the fundamental embryologic error in this condition, but Denda suggested that atresia of developing fourth ventricular foramina was only a part of the syndrome and not its cause, because in some cases reported, the foramina were found to be patent. These patients. Show characteristic clinical symptoms, signs and radiological findings and should suggest the correct diagnosis. This syndrome was one of the first cause of hydrocephalus to be treated successfully by surgery. We are reporting one case of this cyst encountered recently at Yonsei University Medical Center.
Academic Medical Centers
;
Dandy-Walker Syndrome*
;
Diagnosis
;
Fourth Ventricle
;
Humans
;
Hydrocephalus
6.Minimum Five-Year Results of Arthroscopic Management with Labral Preservation in Borderline Hip Dysplasia
Dong Hun HAM ; Woo Chull CHUNG ; Soon Ho HUN ; Myung Cheol JUNG
The Journal of the Korean Orthopaedic Association 2022;57(2):115-121
Purpose:
This study examined the patient-reported outcome scores at mid-term follow-up after arthroscopic labral preservation in patients with borderline hip dysplasia.
Materials and Methods:
Data were collected retrospectively from patients who underwent arthroscopic labral preservation. Among the 61 patients classified with hip dysplasia, patients with arthritis beyond Tönnis grade II were excluded, Patients with subchondral bony exposure were excluded even if they had arthritis of Tönnis grade I. Forty-two patients with borderline hip dysplasia were enrolled among patients whose lateral center edge angle (LCEA) was between 18° and 25°. The PRO scores including the modified Harris hip score (mHHS), hip outcome score activities of daily living (HOS-ADL), hip outcome score sport-specific subscale (HOS-SSS) and visual analog scale (VAS), were collected and compared preoperatively, and then at one year and a minimum of five years after surgery.
Results:
The mean preoperative LCEA and Tönnis angle were 20.9° (range, 18° to 25°) and 6.3° (range, 0° to 18°), respectively. The mean follow-up was 64.8 (range, 60 to 84) months. The mean mHHS increased from 73.5 before surgery to 86.2 in the fifth year after surgery (p<0.01), the mean HOS-ADL from 70.5% before surgery to 84.9% in the fifth year after surgery (p<0.01), and the mean HOS-SSS from 51.4 before surgery to 69.4 in the fifth year after surgery (p<0.01). The mean VAS score improved from 6.3 before surgery to 1.5 in the fifth year after surgery (p<0.01).
Conclusion
Arthroscopic labral preservation performed in appropriately selected patients with borderline dysplasia showed good results at mid-term follow-up. In borderline hip dysplasia without the progress of osteoarthritis and subchondral bone exposure, arthroscopic labral preservation may be considered a good and less invasive option.
7.Electron Microscopic Study of Enalapril Effect on Left Ventricular Hypertrophy in Spontaneously Hypertensive Rat.
Bang Hun LEE ; Jung Hyun KIM ; Heon Kil LIM ; Chung Kyun LEE ; Il Gyun CHOI
Korean Circulation Journal 1990;20(2):232-241
Left ventricular hypertrophy is a compensatory response to hemodynamic overload secondary to an increased systemic resistance. This increase, however, is not the only cause of hypertrophy, and there are other factors which can have a significant effect on its incidence. To determine whether chronic antihypertensive therapy by enalapril modifies the cellular and subcellular changes of left ventricular hypertrophy observed in spontaneously hypertensive rats(SHR), 20-weeks-old SHR were treated for 22 weeks with enalapril(2mg/kg) and compared with normotensive Wister-Kyoto rats and not-treated SHR. Systolic blood pressure in enalapril-treated SHR was significantly lowered after 22 weeks compared with that of untreated control SHR group. Myocytes were reduced in size and fibrination seen in cardiac muscle fibers of control SHR was decreased in treated SHR group. Myofibrils appeared to be irregular in shape and myofilaments are decreased in control SHR but in enalapril-treated SHR the diameter and length of the myofilament became turned to regular forms. These results suggest that, enalapril, angiotensin converting enzyme inhibitor, may regress hypertrophy and some subcellular changes may be modified by enalapril.
Animals
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Blood Pressure
;
Enalapril*
;
Fibrin
;
Hemodynamics
;
Hypertrophy
;
Hypertrophy, Left Ventricular*
;
Incidence
;
Muscle Cells
;
Myocardium
;
Myofibrils
;
Peptidyl-Dipeptidase A
;
Rats
;
Rats, Inbred SHR*
8.Electronmicroscopic Study of Collodion Baby.
Jung Bock LEE ; Seung Hun LEE ; Sung Nack LEE ; Chung Sook KIM
Korean Journal of Dermatology 1981;19(1):93-98
Collodion baby is one of the rare congenital ichthyosiform dermatoses first described by Seeligmann in 1841. It is a phenotypic expression of several genotypes such as aex-linked ichthyosis and bullous and non-bullous congenital ichthyosiform erythroderma. The infant is enveloped in a smooth and shiny collodion-like membrane at birth, which temporarily may deform the facial feature and extremities. The skin clears almost completely in the first month of life and remains free of ichthyosis. Etiology of this condition is still controversy, but it has been known that abnormalities of other organs are not accompanied but prematurity frequently. We present two cases of collodion baby with electron microscopic findings. In the upper stratum spinosum, keratinosomes and desomoaomes were increased in the keratinocytes, and intercellular spaces widened, however, desmosomes and tonofilaments were intact. These findings were similar to those of nonbullous congenital ichthyosiform erythroderma. But in some widened intercellular spaces of the upper stratum spinosum, multiple finely granular electron dense particles were seen within large round membranous structures.
Collodion*
;
Desmosomes
;
Extracellular Space
;
Extremities
;
Genotype
;
Humans
;
Ichthyosiform Erythroderma, Congenital
;
Ichthyosis
;
Ichthyosis, Lamellar
;
Infant
;
Intermediate Filaments
;
Keratinocytes
;
Membranes
;
Parturition
;
Skin
;
Skin Diseases
9.Levels of Soluble Interleukin-2 Receptors in Serum of Patients with Behçet's Disease.
Won HUR ; Seung Hun LEE ; Dongsik BANG ; Sungnack LEE ; Jung Chul KIM ; Tai Ho CHUNG
Annals of Dermatology 1993;5(1):13-16
BACKGROUND: Interleukin-2 receptor (IL-2) is expressed and released predominantly activated T lymphocyte. Increased serum levels of soluble IL-2R have been noted in a variety of autoimmune diseases and in conditions associated with T lymphocyte activation. OBJECTIVE: We aimed to examine whether the T lymphocyte activation has any association with the pathogenesis of Behçet's disease. METHOD: We have measured the serum level of soluble IL-2R in serum samples obtained from 67 patients with Behçet's disease and 30 healthy people as a control group, using a double-antibody sandwich enzyme-linked immunosorbent assay technique. RESULTS: Serum soluble IL-2R levels were found to be significantly elevated in the group of Behçet's disease as compared with the control group. No significant differences were found within clinical subtypes of Behçet's disease. CONCLUSION: These findings suggest the presence of an ongoing T lymphocyte activation in this disease process.
Autoimmune Diseases
;
Enzyme-Linked Immunosorbent Assay
;
Humans
;
Interleukin-2*
;
Lymphocyte Activation
;
Lymphocytes
;
Methods
;
Receptors, Interleukin-2*
10.Levels of Soluble Interleukin-2 Receptors in Serum of Patients with Behçet's Disease.
Won HUR ; Seung Hun LEE ; Dongsik BANG ; Sungnack LEE ; Jung Chul KIM ; Tai Ho CHUNG
Annals of Dermatology 1993;5(1):13-16
BACKGROUND: Interleukin-2 receptor (IL-2) is expressed and released predominantly activated T lymphocyte. Increased serum levels of soluble IL-2R have been noted in a variety of autoimmune diseases and in conditions associated with T lymphocyte activation. OBJECTIVE: We aimed to examine whether the T lymphocyte activation has any association with the pathogenesis of Behçet's disease. METHOD: We have measured the serum level of soluble IL-2R in serum samples obtained from 67 patients with Behçet's disease and 30 healthy people as a control group, using a double-antibody sandwich enzyme-linked immunosorbent assay technique. RESULTS: Serum soluble IL-2R levels were found to be significantly elevated in the group of Behçet's disease as compared with the control group. No significant differences were found within clinical subtypes of Behçet's disease. CONCLUSION: These findings suggest the presence of an ongoing T lymphocyte activation in this disease process.
Autoimmune Diseases
;
Enzyme-Linked Immunosorbent Assay
;
Humans
;
Interleukin-2*
;
Lymphocyte Activation
;
Lymphocytes
;
Methods
;
Receptors, Interleukin-2*