1.Clinical Study and Therapeutic Experience in Tinea Versicolor.
Jae Hong KIM ; Jin Tack LEE ; Eui Chul JEONG
Korean Journal of Dermatology 1986;24(1):55-60
Fifty-six patients with tinea versicolor were studied clinically and therapeutically, from July 1984 to August 1985, at the Department of Dermatology, Hanyang University. L atients were treated with 20g sodium thiosulfate solution, 1g isoconazole nitrate cream, lg bifonazole cream and. oral ketoconazole. The result obtained were as follows: 1. The average age of all patients at visit was RO. 1 years, the oldest patient was 72 year-old and the youngest patient was 13 year-old. The male to female ratio was 3. 7: 1. 2. Distribution of lesions were anterior chest(26.8%), back(23.9%), abdomen (19%), axilla (17%), neck(6. 3%), pubic area(4. 2%), upper extremities(1. 4%), hip(0.7%) and lower extremities(0.7%). The incidence of hyperpigmented lesions was 76. 8%, and that of hypopigmented lesions was 23. 2g. 3. Average of treatment duration in each trial group indicated 3. 71-I--0 83 weeks (M+SD) in 20g sodium thiosulfate regimen group, 3. 07+ 0. 73 weeks in 1g isoconazole nitrate, 3.29+1.14 weeks in bifonazole, R. 00+0. 68 weeks in oral ketoconazole. No treatment results show statistically significant differences among the trial groups.
Abdomen
;
Adolescent
;
Aged
;
Axilla
;
Dermatology
;
Female
;
Humans
;
Incidence
;
Ketoconazole
;
Male
;
Sodium
;
Tinea Versicolor*
;
Tinea*
2.Role of Sp Family Transcription Factors in Growth Hormone Receptor Gene Expression.
Jeong Won SHIN ; Jae Hong YU ; Ren Zhe AN
Journal of Korean Society of Pediatric Endocrinology 2000;5(2):151-162
PURPOSE: The growth hormone receptor(GHR) is essential for the actions of growth hormone on postnatal growth and metabolism. GHR transcripts are characterized by the presence of disparate 5'untranslated exons. In contrast to L1 transcript, factors regulating the expression of the GC rich L2 transcript have remained unidentified. The purpose of this study is in order to characterize the mechanisms regulating expression of the L2 transcript in the murine GHR gene METHODS: Transient transfection experiments including deletional analysis and co-transfection assay were performed to find a region containing promoter activity in the L2 5'flanking sequence using BNCL2(mouse liver) cells, CV-1(African green monkey kidney) cells, HRP.1 trophoblasts and Drosophila Schneider(SL2) cells. Sequencing analysis was performed to find the region contained consensus binding sites for transcription factors. Standard gel shift(Electrophoretic mobility shift assay, EMSA) and supershift analysis using liver nuclear extracts was performed to establish proteins(transcription factors) bound this regulatory element. RESULTS: The 5'flanking region of the L2 untranslated region(UTR) exhibited promoter activity in BNCL2(mouse liver), CV-1(monkey kidney) cells and HRP.1 trophoblasts. Deletional analyses indicated the presence of a Sp binding site important for transcription of the L2 UTR and localized the major regulatory region within 75 bp of the 5'transcription start site. Sequencing analyses revealed the region contained consensus binding sites for the Sp family of transcription factors. EMSA and supershift EMSA revealed that in mouse liver nuclear extracts that Spl and Sp3 bound to this cis-element. Functional studies in Drosophila SL2 cells and BNCL2(mouse liver) cells established the ability of Sp3 and Sp1 to stimulate transcriptional activity via this cis-element. Functional studies in Drosophila SL2 cells demonstrated a functional interaction between Sp3 and Sp1 at this DNA-binding site. CONCLUSION: Sp family transcription factors play a role in regulation of L2 transcript gene expression in the 5'flanking region of the murine GHR gene.
Animals
;
Binding Sites
;
Cercopithecus aethiops
;
Consensus
;
Drosophila
;
Electrophoretic Mobility Shift Assay
;
Exons
;
Gene Expression
;
Growth Hormone*
;
Humans
;
Liver
;
Metabolism
;
Mice
;
Receptors, Somatotropin*
;
Regulatory Sequences, Nucleic Acid
;
Transcription Factors*
;
Transfection
;
Trophoblasts
3.Two Cases of Cutaneous Cytomegalovirus Infection in Immunocompromised Patients.
Jae Hong PARK ; Jeong Joon OH ; Eil Soo LEE
Annals of Dermatology 2004;16(2):67-70
Cytomegalovirus (CMV) is a major cause of morbidity and mortality in immunocompromised patients. CMV can cause pneumonia, retinitis, gastrointestinal ulcers, and widely disseminated disease, but cutaneous CMV is rare. We report two cases of cutaneous CMV infection presenting as perianal ulcers. A 54 year-old male who had liver transplantation and a 72-year-old male, who was treated with chemotherapy for angioimmunoblastic T-cell lymphoma, presented with perianal ulcers and had systemic symptoms of CMV infection with CMV antigenemia. They had multiple ulcerations with erythematous bases on the perianal area, and histopathologic examinations showed large atypical cytomegalic cells in the dermis, and immunohistochemical stains, with the anti-CMV antibody showed positive reactions.
Aged
;
Coloring Agents
;
Cytomegalovirus Infections*
;
Cytomegalovirus*
;
Dermis
;
Drug Therapy
;
Humans
;
Immunocompromised Host*
;
Liver Transplantation
;
Lymphoma, T-Cell
;
Male
;
Mortality
;
Pneumonia
;
Retinitis
;
Ulcer
4.Three Cases of Congenital Adrenal Hyperplasia Owing to Multiple Mutations of CYP21 Gene.
Jun HEO ; Jae Hong YU ; Dong Ki JEONG
Journal of Korean Society of Pediatric Endocrinology 2001;6(2):176-181
Congenital adrenal hyperplasia(CAH) results from an inherited defect in enzymatic steps required to synthesize cortisol from cholesterol. 21-hydroxylase deficiency accounts for 95% cases of CAH. We have analyzed CYP21 genes of CAH by PCR direct sequencing. Our results shows three cases of CAH owing to multiple mutations of CYP21 gene; first case, IVS2AS, A/G, -13, Ile172Asn; second case, IVS2AS, A/G, -13, Ile236Asn, Val237Glu, Met239Lys; third case, Ile172Asn, C to G at 1590nt, Val281Leu, Arg484Pro, G to A at 2697nt. Mutations such as Ile236Asn, Val237Glu, Met239Lys, and Arg484Pro are first noted in Korea.
Adrenal Hyperplasia, Congenital*
;
Cholesterol
;
Hydrocortisone
;
Korea
;
Polymerase Chain Reaction
;
Steroid 21-Hydroxylase
5.A Study on Postgonococcal Urethritis.
Eui Chul JEONG ; Jae Hong KIM ; Joong Hwan KIM
Korean Journal of Dermatology 1986;24(2):242-248
The subject were 653 male patients with uncomplicated gonorrhea at the VD Clinic of Choong Ku Public Health Center in Seoul from January to November 1985. 653 male patients with uncomplicated gonococcal infection were treated one of the following regimens. Five treatment regimens used were 2, 0 gm spectinomycin single 1M, 4 0 mega unit fortified procain penicillin G+2. 0 gm kanamycin sulfate IM preceded by 1 pgm probenecid PO, 6.0 mega unit fortified procain penicillin G+2 pgm kanamycin sulfate IM preceded by 1. 0 gm probenecid PO, 5, 0 rnega unit aqueous crystaline penicillin+2. 0 gm kanamycin sulfate irn preceded by 1, 0 gm probenecid PO and 9 tablets of cotrimoxazole+ 2. 0 gm kanamycin sulfate IM. There were no significant differences in the incidence of PGU among the five treatment groups. The overall PGU rate was 67.3% 59.2% and 53.6% at 3~5, 7~10 and 14 days after treatment respectively. The incidence of PGU at 7-10 days was not significantly higher than that of at 14 days after treatment. It is suggested that it is best to test PGU at 7 days after treatment. Because the longer one waits, the harder to follow the patients, and in earlier period, post-inflammatory irritation might be too frequent. It is also suggested that at 3 5 days after treatment examination of urethritis might serve to compare the effect of treatment regimens on the incidence of PGU.
Gonorrhea
;
Humans
;
Incidence
;
Kanamycin
;
Male
;
Penicillins
;
Probenecid
;
Public Health
;
Seoul
;
Spectinomycin
;
Tablets
;
Urethritis*
6.Freeman-Sheldon Syndrome: Report of Two Cases in a Family
Jae In AHN ; Byoung Suck KIM ; Yeong Seong KIM ; Jeong HONG
The Journal of the Korean Orthopaedic Association 1996;31(4):937-941
Freeman-Sheldon Syndrome is one of the very rare genetic diseases which primarily affects face, hands and feet. At first, Freeman and Sheldon described this syndrome as cranio-carpo-tarsal dystrophy in 1938 and later Burian, as "whistling face" syndrome in 1963. There were 60 cases of reports in the world up to now, and only one paper with 5 cases in a family was reported in Korea. The authors report 2 cases of Freeman-Sheldon Syndrome associated with bilateral inguinal hernias and undescended tests in a family, briefly review the literature and alert orthopaedic surgeons to this condition.
Cryptorchidism
;
Foot
;
Hand
;
Hernia, Inguinal
;
Humans
;
Korea
;
Male
;
Surgeons
7.Clinical application of hydroxyapatite(surgibone(r)).
Jung Soo HONG ; Jeong Chul KIM ; Jae Ho JEONG ; Dong Bo SUH ; Jung Hyun SEUL
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1993;20(2):333-342
No abstract available.
8.Prognostic Factors in Neurologic Deficit after Thoracic and Lumbar Spine Fracture
Young Gi HONG ; Keon PARK ; Jae Do KIM ; Jeong HWAN ; Jeong Ho PARK
The Journal of the Korean Orthopaedic Association 1996;31(4):688-694
The thoracic and lumbar spine fractures were usually combined with neurological deficit. But the prognostic factors in degree of neurological damage and process of the recovery are controversial. The purpose of this study is to evaluate the factors affected neurological injury and the recovery. The 31 cases who had been performed surgical interventions due to traumatic thoracic or lumbar spine fractures with the neurological deficits were studied according to the radiographic findings of the spinal columns and neurological changes of the injured cord and/or the roots. The duration of mean follow-up was 32.6 months, and all cases were evaluated by motor index score and Frankel grade. Total cases were divided into complete paralytic (N=8) and partial paralytic(N=23) group. In incomplete paraplegia group, the neurological recovery rate was better than complete group(P < 0.001) and neurological recovery period was shorter than complete group (P=0.005). The neurologic deficits according to the Frankel grade were higher in Chance fracture, flexion-distraction and translation (complete paraplegia: 4/7 cases, 57.1%) than unstable bursting fracture (complete paraplegia: 4/24 cases, 16.7%)(P=0.031). The recovery rate of Chance fracture, flexion-distraction and translation were worse than unstable bursting fracture (0.001). The fracture which occurred in T5-11 showed higher incidence of complete paraplegia(75%) compared with that of the T12-L1(30.8%) & L2-4(7.1%)(p=0.021). The neurological recovery in motor index score in L2-4 was higher than T5-11 or T12-L1(P=0.0017). There was no correlation in kyphotic deformity and anterior body height loss between complete and incomplete paraplegia groups. But the A-P diameter of compromised neural canal showed significant difference between complete and incomplete paraplegia group(P=0.027)
Body Height
;
Congenital Abnormalities
;
Follow-Up Studies
;
Incidence
;
Neural Tube
;
Neurologic Manifestations
;
Paraplegia
;
Spine
9.A Case of Mucoepidermoid Carcinoma in Pulmonary Tuberculosis Patient.
Jae Man JEONG ; Ju Young SONG ; Jae Rack HONG ; Young Jun KIM ; Moon Shik KIM
Tuberculosis and Respiratory Diseases 1994;41(4):429-434
Mucoepidermoid carcinoma of lung are rare carcinoma arising from the submucosal glands tissue of the proximal tracheobronchial tree. The carcinoma can be divided into low grade and high grade varienties. The most important factors in the prognosis include histological grading and the ability to achieve a complete surgical resection. We experienced a case of high grade mucoepidermoid carcinoma in pulmonary tuberculosis patient of 67 years old male who has been suffered from left chest pain for several weeks. He was not treated and died seventeen months later.
Carcinoma, Mucoepidermoid*
;
Chest Pain
;
Humans
;
Lung
;
Male
;
Prognosis
;
Trees
;
Tuberculosis, Pulmonary*