1.A Wide Muscle-splitting Approach to the Lumbosacral Spine
The Journal of the Korean Orthopaedic Association 1986;21(6):1119-1125
20 patients with lumbosacral disorder underwent anterior spinal fusion using wide muscle splitting approach. The approach has considerable advantages over the usual muscle cutting approach or the transperitoneal approach commonly employed for this incision. The advantages of this approach are as follows: 1. The approach to the lesion site is safe and accurate. 2. The operation field is wide. 3. It is less destructive to the abdominal wall. 4, The defect left in iliac crest after removal of bone graft can be covered with external oblique layer. 5. The exposure given to the Ls-S1 intervertebral disc is superior to that given by the Rutherford Morrison approach.
Abdominal Wall
;
Humans
;
Intervertebral Disc
;
Spinal Fusion
;
Spine
;
Transplants
2.The clinical effect of vigabatrin in refractory pediatric epilepsies.
Ki Joong KIM ; Baeck Hee LEE ; Se Hee HWANG ; Yong Seung HWANG
Journal of the Korean Child Neurology Society 1993;1(2):91-96
No abstract available.
Epilepsy*
;
Vigabatrin*
3.A Case of Piouitary Hyperplasia with Retardation due to Primary Hypothyroidism.
Hong Seung KIM ; Choon Hee CHUNG ; Young Goo SHIN ; Bong Ki LEE
Journal of Korean Society of Endocrinology 1997;12(4):589-595
Primary hypothyroidism can result in reactive enlargement of the pituitary gland which is indistinguishable from primary pituitary lesions in clinical presentation and on magnetic resonance imaging. A 17-year-old girl came to the hospital due to short stature, general weakness and galac-torrhea. The magnetic resonance imaging (MRI) study showed pitutary enlargement. The hormone study showed hyperprolactinemia, decreased basal growth hormone level and primary hypothyroi-dism. By thyroid replacement therapy only, mass was successfully regressed on follow up MRI after 4 months, and growth acceleration could be achieved.
Acceleration
;
Adolescent
;
Female
;
Follow-Up Studies
;
Growth Hormone
;
Humans
;
Hyperplasia*
;
Hyperprolactinemia
;
Hypothyroidism*
;
Magnetic Resonance Imaging
;
Pituitary Gland
;
Thyroid Gland
4.Anticardiolipin Antibody (ACA) and Lupus Anticoagulant (LA): Association with Vascular Access Occlusion in Hemodialysis (HD) Patients.
Duk Hee KANG ; Seung Ki RYU ; Sung Nam KIM ; Kyun Il YOON ; Yoon Ha LEE
Korean Journal of Medicine 1997;53(5):661-670
OBJECTIVES: Anticardiolipin antibody (ACA) and lupus anticoagulant (LA) are acquired antiphospholipid antibodies (APAs), which are regarded as important risk factors far vascular thrombosis and recurrent fetal loss. Although the clinical relevance of APAs in dialysis patients is uncertain, recent studies have suggested that APAs are involved in bioincompatibility and thrombogenic complications in hemadialysis (HD) patients. METHOD: We performed a cross sectional study of ACA and LA in 50 stable HD patients and their 68 vascular accesses (52 native arteriovenous fistulae and 16 synthetic arterovenous grafts), with the analysis of factors associated with the presence of APAs and the retrospective evaluation of vascular access occlusion (VAO). LA was assessed by platelet neutralization method whereas IgG-ACA was measured by a solid phase ELISA. Values higher than 23GPLU/ml (IgG phospholipid units) were considered to be positive for IgG-ACA and positive values for LA was more than 8 seconds in prolongation of the clotting time with human platelet lysate. Vascular access survival was assessed by Kaplan- Meier method, RESULTS: The mean age of the subject (M:F 21:29) was 46 years and the mean duration of hemodialysis was 49 months. The frequency of VAO in entire subjects was 0.45+/-0.98 episodes/patient year. The median value of IgG-ACA was 16.0 GPLU/ml with a distribution from 2.7 to 46.1GPLU/ ml. The median titer of I.A was 4.5 (3.1-45.6) seconds. Fourteen patients (28%) were found to have at least one episode of VAO. In spite of comparable clinical and biochemical data according to the presence of VAO, the titers of IgG-ACA (13.6+/-7.7 vs, 20.3+/-8.7GPLIJ/ml, P<0.05) and LA (4.5+/-2.9 vs. 11.7 +/-12.6sec, P<0.05) were significantly higher in VAO group. Six out of 50 patients(12%) had an increased titer of IgG-ACA and LA was found in 11 patients(22%). No patients were positive for ACA and LA simultaneously. There was no significant difference in sex, etiology of ESRD, diabetic status, the dosage of heparin during HD or the amount of erythropoietin administered according to the presence of APAs. We could not find any significant correlation between the titer of APAs and age, duration of dialysis, blood pressure, platelet count and biochemical parameters. In the patients with positive ACA, the frequency of VAO was 1.05+/-0.12 episodes/patient year, which was significantly higher than patients without ACA (0.33+/-0.17 episodes/ patient year, P<0.05). In the patients with the presence of LA(1.06+/-0.43 vs. 0.12+/-0.06 episodes/ patients year, P<0.01). The median vascular access survival time in IgG-ACA positive patients (32.7 months) was significantly decreased compared to 66.8 months in IgG-ACA negative group. CONCLUSION: Our data suggest that the presence of APAs (ACA and/or LA) affects the event-free vascular access survival in HD patients. Therefore the evaluation of APAs status have to be included in the diagnostic strategies for the patients with recurrent VAO. Further studies are necessary to explore the pharmacologic intervention method to decrease APAs and prevent VAO in HD patients.
Antibodies, Anticardiolipin*
;
Antibodies, Antiphospholipid
;
Arteriovenous Fistula
;
Blood Platelets
;
Blood Pressure
;
Dialysis
;
Enzyme-Linked Immunosorbent Assay
;
Erythropoietin
;
Heparin
;
Humans
;
Kidney Failure, Chronic
;
Lupus Coagulation Inhibitor*
;
Platelet Count
;
Renal Dialysis*
;
Retrospective Studies
;
Risk Factors
;
Thrombosis
5.Comparison of tuberculin skin test results and adverse reactions following BCG vaccination in various infant groups of different ages.
In Seung PARK ; Dong Ki HAN ; Ho Joon LIM ; Sung Hee OH ; Hahng LEE
Journal of the Korean Pediatric Society 1993;36(9):1300-1307
Most authorities including WHO recommended immununizing infants with BCG as early as possible in areas prevalent with tuberculosis, however the optimal time for immunization has not well been characterized. Therefore the investigation was undertaken by vaccinating various infant groups of different ages with BCG and subsequently evaluating for adverse effects and tuberculin reactions, in order to contribute to undestanding the optimal time for immunization. Four hundred eighty three infants from the newborn nursery and the well baby clinic of Hanyang University Hospital who had no family history of tuberculosis were divided into three groups; group I of infants immunized within 7 days after birth, group II of infants immunized at about 1 month of age and group III of infants immunized at about 3 months of age. To each infant 0.1 ml of BCG(Institute Merieux, France) was administered intradermaly and approximately 3 months later tuberculin skin test using 5 TU PPD (NIH, Korea) was performed. Adverse reactions following BCG vaccination such as temperature elevation, induration alone or with suppuration at or near the injection site, and lymph node enlargement were also analyzed. The summary of the results is as follows. 1) Distribution of diameters of induration on tuberculin skin test illustrated incomplete bimodal configuration in all three different age groups. The means 2 standard deviations of diameters of indurations distributed on the main bells were 10.07 4.52 mm in group I, 10.65 3.82 mm in group II, and 10.83 5.08 mm in group III, and were not significantly different. 2) Criteria for positive tuberculin reaction was diameters of indurations equal to or greater than 6mm, 2 standard deviations below the mean values of diameters of indurations on the main bells. 3) The positive tuberculin reaction rates of 85.8% in group II and 88.6% in group III were significantly greater than 74.1% in group I. 4) Incidence of complications following BCG vaccination including temperature elevation, induration with suppuration, and localized lymphadenopathy was not different among three groups and the serious complications such as temperature elevation and lymphadenopathy were minimal. The data indicate that it is appropriate to immunize infants with BCG at about one month of age and the incidence of complications following BCG vaccination was not different among three infant groups of different ages.
Humans
;
Immunization
;
Incidence
;
Infant*
;
Infant, Newborn
;
Lymph Nodes
;
Lymphatic Diseases
;
Mycobacterium bovis*
;
Nurseries
;
Parturition
;
Skin Tests*
;
Skin*
;
Suppuration
;
Tuberculin Test
;
Tuberculin*
;
Tuberculosis
;
Vaccination*
6.Median sternotomy for bilateral resection or plication of bullae.
Hee Chul PARK ; Suck Jun KONG ; Ho Seung SHIN ; Bung Joo KIM ; Ki Woo HONG
The Korean Journal of Thoracic and Cardiovascular Surgery 1991;24(2):182-189
No abstract available.
Sternotomy*
7.Evaluation of fibrovascular ingrowth into the hydroxyapatite ocular implant by Tc-MDP bone scintigraphy.
Hee Seung BOM ; Ho Chun SONG ; Ji Yeul KIM ; Sang Ki JEONG ; Young Kul PARK
Korean Journal of Nuclear Medicine 1993;27(2):256-260
No abstract available.
Durapatite*
;
Radionuclide Imaging*
8.Formal charts for quantified Tc-DMSA renal uptake rates.
Tae Yong MOON ; Yong Ki KIM ; Su Hee HWANG ; Chong Byung YOON ; Kyung Tak SEUNG
Korean Journal of Nuclear Medicine 1993;27(2):248-255
No abstract available.
9.Association of HLA-DR and -DQ Genes with Familial Moyamoya Disease in Koreans.
Seok Ho HONG ; Kyu Chang WANG ; Seung Ki KIM ; Byung Kyu CHO ; Myoung Hee PARK
Journal of Korean Neurosurgical Society 2009;46(6):558-563
OBJECTIVE: Moyamoya disease (MMD) is an uncommon cerebrovascular disorder, characterized by progressive occlusion at the terminal portion of the internal carotid artery. Incidence of the disease is high in East Asia and familial MMD accounts for about 15% of the disease. Although the pathogenesis is unknown, association of HLA class I or II alleles with MMD has been reported with conflicting results. We investigated whether there is a difference in HLA class II association between familial and non-familial forms of the disease. METHODS: A total of 70 Korean children with MMD, including 16 familial cases (10 probands), and 207 healthy controls were studied. Among familial cases, only 10 probands were used for the HLA frequency analysis. High resolution HLA-DRB1 and DQB1 genotyping was performed using polymerase chain reaction (PCR)-sequence specific oligonucleotide hybridization and PCR-single strand conformation polymorphism methods. RESULTS: The phenotype frequencies of HLA-DRB1*1302 (70.0%) and DQB1*0609 (40.0%) were significantly increased in familial MMD compared to both controls [vs. 15.5%, corrected p (pc) = 0.008, odds ratio (OR) = 12.76; vs. 4.3%, pc = 0.02, OR = 14.67] and non-familial MMD patients (vs. 14.8%, pc = 0.02, OR = 13.42; vs. 1.9%, pc = 0.02, OR = 35.33). The frequencies of DRB1 and DQB1 alleles in non-familial MMD patients were not significantly different from those in controls. CONCLUSION: Our findings suggest that the genetic polymorphism of HLA class II genes or other closely linked disease relevant gene(s) could be a genetic predisposing factor for familial MMD.
Alleles
;
Carotid Artery, Internal
;
Cerebrovascular Disorders
;
Child
;
Chimera
;
Far East
;
Genes, MHC Class II
;
HLA-DQ Antigens
;
HLA-DR Antigens
;
HLA-DRB1 Chains
;
Humans
;
Incidence
;
Moyamoya Disease
;
Odds Ratio
;
Phenotype
;
Polymerase Chain Reaction
;
Polymorphism, Genetic
10.Case report of pan-peritonitis due to duodenal ulcer perforation associated with comminuted mandibular fracture.
Dong Keun LEE ; In Woong UM ; Kue Hee KIM ; Seung Ki MIN
Journal of the Korean Association of Oral and Maxillofacial Surgeons 1992;18(1):87-90
No abstract available.
Duodenal Ulcer*
;
Mandibular Fractures*