1.A Case of Solitary Keratoacanthoma Originated from Verruca Vulgaris.
Yoon Sung PARK ; Soo Il CHUN ; Chang Jo KOH
Korean Journal of Dermatology 1984;22(3):334-337
Keratoacanthoma is a benign neoplasm that develops as a protruding mass especially on the central part of face, We experienced a case of keratoacanthoma that developed on the nasal vestibule after the eradication of verruca vulgaris on the same site by surgical intervention 3 months before. We treated it with total excision and skin graft.
Keratoacanthoma*
;
Skin
;
Transplants
;
Warts*
2.The Effects of Combination of PDGF-BB and Dexamethasone on Differentiation of MC3T3-E1 Cells.
Jae Mok LEE ; Jo Young SUH ; Sung Jo KIM ; Jeom Il CHOI
The Journal of the Korean Academy of Periodontology 2000;30(1):27-37
To evaluate the effects of Dexamethasone(Dex), Platelet derived growth factor-BB(PDGF) and combination of Dex and PDGF(DP) on the growth and differentiation of MC3T3-E1 cells, Dex(10(-7) M) and PDGF(10 ng/ml) in experimental group were added to the cells at the days 5, 10, 15, 20, 25 and examined for cell proliferation activities, DNA synthesis activities, ALP activities and bone nodule formation. The results were as follows : 1.In Dex group, cell proliferation, DNA synthesis and ALP activities were lower until 15 days when compared to the control group. Bone nodules formation were shown at 10 days. 2.In PDGF group, cell proliferation and DNA synthesis activities were higher until 15 days and ALP activities were lower when compared to the control and Dex groups. Bone nodules formation were shown at 20 days. 3.In DP group, cell proliferation and DNA synthesis activities of PDGF were suppressed by Dex and synergistic effects of combination of Dex and PDGF on ALP activities were shown at days 5 when compared to control and Dex groups. Bone nodules formation activities of Dex were suppressed by PDGF.
Blood Platelets
;
Cell Proliferation
;
Dexamethasone*
;
DNA
3.Bowen's Disease and Internal Malignacy.
Jin Soo KANG ; Soo Il CHUN ; Chang Jo KOH ; Sung Nack LEE
Korean Journal of Dermatology 1980;18(4):313-320
It is well known that Bowen's.disease, a precancerous dermatosis can be associated with internal malignancy. We report 2 cases of Bowen's disease of probable arsenic origin associated with. internal malignancies. Case one, a 55 year-old man, who had the past history of arsenic intake and herb medication for the treatment of suspicious leprosy, had Bowen's disease and arsenical keratosis on his palms and soles with bronchogenic and stomach carcinoma. The other case, a 65 year-old man, who had history of intake of arsenic and herb medicine for epilepsy, had Bowen's disease and squamous cell carcinoma of the skin with stomach cancer. We suggest that in these 2 cases, the ingestion of organic arsenics might be the causative factor for the internal malignancy.
Aged
;
Arsenic
;
Bowen's Disease*
;
Carcinoma, Squamous Cell
;
Eating
;
Epilepsy
;
Humans
;
Keratosis
;
Leprosy
;
Middle Aged
;
Skin
;
Skin Diseases
;
Stomach
;
Stomach Neoplasms
4.Development of PCR Technology for Identification of the Restriction Fragment Length Polymorphism(RFLP) of the Immunoglobulin Allotypes in Periodontal Patients.
Jeom Il CHOI ; Sung Jo KIM ; In Hoo KIM
The Journal of the Korean Academy of Periodontology 1999;29(2):349-354
The present study has been performed to develop a PCR technology to identify human immunoglobulin(Ig) allotypes with restriction fragment length polymorphism(RFLP) using a probe. Genomic DNA were ampilified with PCR tecnology using primers from peripheral blood lymphocytes of 10 periodontal patiens, whose Ig allotypes have been pre-determined by serological tecnique using heagglutination technique. The result indicated that the RFLP patterns could successfully differentiate the Ig allotypes, which suggests that this technology can be developed as a tool useful for population genetics studies.
DNA
;
Genetics, Population
;
Humans
;
Immunoglobulin Allotypes*
;
Immunoglobulins*
;
Lymphocytes
;
Polymerase Chain Reaction*
;
Polymorphism, Restriction Fragment Length
5.Nail - Patella Syndrome.
Soo Il CHUN ; Su Chan KIM ; Chang Jo KOH ; Sung Nack LEE
Korean Journal of Dermatology 1980;18(2):149-153
The nail-patella syndrome is a genetically determined autosomal dominant disease with variabIe expression affectiag tissues of both ectodermal and mesodermal origin. The condition in an individual is characterized chiefly by dysplasia of the fingernails, hypoplastic or absent patellae, deformities or luxation af the head of the radius, and the presence of illiac horns. It is now well established that the locus for the nail-patella syndrome and the locus for the ABO blood groups are closely linked. We report 2 cases of nail-patella syndrome affected a brother and a sister in a family. Our 2 cases, with blood group B, showed dystrophic nails and hypoplastir. patellae.
Animals
;
Blood Group Antigens
;
Congenital Abnormalities
;
Ectoderm
;
Head
;
Horns
;
Humans
;
Mesoderm
;
Nail-Patella Syndrome
;
Nails
;
Patella*
;
Radius
;
Siblings
6.Polymorphisms Linked to Factor IX Gene in Korean Population.
Joong Sik SHIN ; Sung Ro JUNG ; Il Pyo SON ; Yool Hee JO
Korean Journal of Obstetrics and Gynecology 2000;43(11):2038-2044
OBJECTIVE: Linkage analysis is a very useful method for prenatal diagnosis of Hemophilia B, especially when a mutation was not identified. Seven polymorphic markers were studied in Korean populations to evaluate the efficiency for prenatal and carrier diagnosis. METHODS: Subjects of this study was 100 healthy Korean women (200 X-chromosomes). Polymerase chain reacton-restriction fragment length polymorphism (PCR-RFLP) method was used to detect SalI, MseI, NruI, DdeI, XmnI, TaqI and HhaI polymorphisms. RESULTS: SalI (-) allele showed the frequency of 0.355 and SalI(+) allele 0.645. MseI(-) allele was 0.645 in frequency and MseI(+) allele was 0.355. SalI and MseI polymorphisms were in complete linkage disequilibrium. And no increase was expected in overall heterozygosity with these two polymorphisms. NruI(-) allele frequency was 0.855 and NruI(+) was 0.145. There was no polymorphism of DdeI, XmnI and TaqI marker systems in Korean population. In HhaI polymorphism, allele frequencies were estimated that HhaI(-) is 0.82 and HhaI(+) is 0.18. CONCLUSION: Only SalI, NruI and HhaI polymorphisms are useful for the diagnosis of hemophilia B in Korean population. Expected heterozygosity for above 3 poylmorphic markers was estimated to be 0.723, and 71 of 100 female subjects were heterozygous for at least one marker system. Korean population showed relatively low extent of polymorphisms compared to Caucasians, Blacks and Japanese. For the effective prenatal diagnosis of hemophilia B with linkage analysis, other polymorphic markers should be evaluated.
African Continental Ancestry Group
;
Alleles
;
Asian Continental Ancestry Group
;
Diagnosis
;
Factor IX*
;
Female
;
Gene Frequency
;
Hemophilia B
;
Humans
;
Linkage Disequilibrium
;
Prenatal Diagnosis
7.A Case of Penile Horn.
Kyung Hoon CHANG ; Yoon Sung PARK ; Soo Il CHUN ; Chang Jo KOH
Korean Journal of Dermatology 1984;22(3):327-329
Penile Horn occurs as a single or multiple lesions. It usually starts as warty growth that later becomes hyperkeratotic and assumes the appearance of a horn. A 22-year-old male patient was presented with a slow growing, asymptomatic, dark brownish colored, corn-shaped, protruding mass on prepuce of the penis for 5 months. Histopathologic finding showed verruca vulgaris. We think that penile horn in this case may be come from verruca vulgaris.
Animals
;
Horns*
;
Humans
;
Male
;
Penis
;
Warts
;
Young Adult
8.Cellular and Humoral Immune Responses to Sequential Periodontopathic Bacterial Immunization in Animal Model.
Soo Kyung JEON ; Sung Jo KIM ; Jeom Il CHOI
The Journal of the Korean Academy of Periodontology 2000;30(3):687-698
Antigen-specific T cell clones were obtained from mice immunized with Fusobacterium nucleatum ATCC 10953(F. nucleatum) and/or Porphyromonas gingivalis 381(P. gingivalis). 10 Balb/c mice per group were immunized with F. nucleatum followed by P. gingivalis, or with P. gingivalis alone by intraperitoneal injection of viable microorganisms. Spleen T cells were isolated and stimulated in vitro with viable P. gingivalis cells to establish P. gingivalis-specific T cell clones. T cell phenotypes and cytokine profiles were determined along with T cell responsiveness to F. nucleatum or P. gingivalis. Serum IgG antibody titers to F. nucleatum or P. gingivalis were also determined by ELISA. All the T cell clones derived from mice immunized with F. nucleatum followed by P. gingivalis demonstrated Th2 subsets, while those from mice immunized with P. gingivalis alone demonstrated Th1 subsets based on the flow cytometric analysis and cytokine profiles, All T cells clones from both groups were cross-reactive to both P. gingivalis and F. nucleatum antigens. Phenotypes of T cell clones were all positive for CD4. Mean post-immune serum IgG antibody levels to F. nucleatum or P. gingivalis were significantly higher than the preimmune levels(p<0.01, respectively). There were no significant differences in the antibody titers between the two groups. It was concluded that P. gingivalis-specific T cells initially primed by cross-reactive F. nucleatum antigens were polarized to Th2 subsets, while T cells stimulated with P. gingivalis alone maintained the profile of Th1 subset.
Animals*
;
Clone Cells
;
Enzyme-Linked Immunosorbent Assay
;
Fusobacterium nucleatum
;
Immunity, Humoral*
;
Immunization*
;
Immunoglobulin G
;
Injections, Intraperitoneal
;
Mice
;
Models, Animal*
;
Phenotype
;
Porphyromonas gingivalis
;
Spleen
;
T-Lymphocytes
9.Prior Exposure of Mice to Fusobacterium Nucleatum Modulates Host Response to Porphyromonas Gingivalis.
Han Yong SON ; Sung Jo KIM ; Jeom Il CHOI
The Journal of the Korean Academy of Periodontology 2000;30(3):675-685
Multiple periodontal pathogens sequentially colonize the subgingival niche during the conversion from gingivitis to destructive periodontal disease. An animal model of sequential immunization with key periodontal pathogens has been developed to determine whether T and B lymppocyte effector functions are skewed and fail to protect the host from pathogenic challenge. The present study was performed to evaluate immunomodulatory effect of exposure to Fusobacterium nucleatum(F. nucleatum) prior to Porphyromonas gingivalis(P.gingivalis). Group 1(control) mice were immunized with phosphate-buffered saline, Group 2 were immunized with F. nucleatum prior to P. gingivalis, while Group 3 were immunized P. gingivalis alone. All the T cell clones derived from Group 2 demonstrated type 2 helper T cell clone(Th2 subsets), while those from Group 3 mice demonstrated Th1 subsets. Exposure of mice to F. nucleatum prior to P. gingivalis interfered with opsonophagocytosis function of sera against P. gingivalis. In adoptive T cell transfer experiments, in vivo protective capacity type 2 helper T cell clones(Th2) from Group 2 was significantly lower than type 1 helper T cell clones(Th1) from Group 3 against the lethal dose infection of P. gingivalis. Western blot analysis indicated the different pattern of recognition of P. gingivalis fimbrial proteins between sera from Group 2 and Group 3. In conclusion, these study suggest that colonization of the subgingival niche by F. nucleatum prior to the periodontal pathogen, P. gingivalis, modulates the host immune responses to P. gingivalis at humoral, cellular and molecular levels.
Animals
;
Blotting, Western
;
Clone Cells
;
Colon
;
Fusobacterium nucleatum*
;
Fusobacterium*
;
Gingivitis
;
Immunization
;
Mice*
;
Models, Animal
;
Periodontal Diseases
;
Porphyromonas gingivalis*
;
Porphyromonas*
10.Epitope specificity of Porphyromonas gingivalis heat shock protein for T-cell and/or B-cell in human atherosclerosis.
Jung Gyu BAK ; Sung Jo KIM ; Jeom Il CHOI
The Journal of the Korean Academy of Periodontology 2003;33(2):179-191
Since periodontal infections are suggested as risk factors for the development of cardiovascular diseases, the present study was performed to evaluate the T cell immune responses specific to Porphylomonas gingivalis(P. gingivalis) heat shock protein(hsp) 60 and T-cell and B-cell epitope specificities for P. gingivalis hsp60 in atherosclerosis. Anti-P. gingivalis IgG antibody titers were elevated in all patients. We could establish P. gingivalis hsp-specific T cell lines from the atheroma lesions, a mixture of CD4+ and CD8+ cells producing the cytokines characteristic of both Th1 and Th2 subsets. of 108 overlapping synthetic peptides spanning whole P. gingivalis hsp60 molecule, ten peptides with common epitopes specificities for both T-cell and B-cell were identified. it was concluded that P. gingivalis hsp60 might be involved in the immunoregulatory process of atherosclerotic diseases with epitope specificities.
Atherosclerosis*
;
B-Lymphocytes*
;
Cardiovascular Diseases
;
Cell Line
;
Cytokines
;
Epitopes
;
Epitopes, B-Lymphocyte
;
Heat-Shock Proteins*
;
Hot Temperature*
;
Humans*
;
Immunoglobulin G
;
Peptides
;
Plaque, Atherosclerotic
;
Porphyromonas gingivalis*
;
Porphyromonas*
;
Risk Factors
;
Sensitivity and Specificity*
;
Shock
;
T-Lymphocytes*