1.Need for Tissue Banking and KMA's Stand.
Journal of the Korean Medical Association 2001;44(11):1148-1150
No abstract available.
Tissue Banks*
2.Doctor's Strike-One Year Later.
Journal of the Korean Medical Association 2001;44(12):1266-1269
No abstract available.
3.The application of TD (Touch-Down) PCR in Diagnosis of leprosy and Detection of MDT-resistant M. leprae.
Se Kon KIM ; Seong Beom LEE ; Tae Jin KANG ; Gue Tae CHAE
Korean Leprosy Bulletin 2001;34(2):13-21
There are several methods for diagnosis of leprosy, including AFB stain, the measurement of PGL-1 (phenolic glycolipid - 1) antigen titer, and DNA-PCR. In this study, we have used the DNA-PCR amplifying the RLEP repetitive sequence. Our result showed that the RLEP primer offered the more sensitive detection and identification of M. leprae DNA in clinical specimens, compared with the other primer, for example, 18-kDa antigen gene. To screen the resistant M. leprae strain of MDT (Multi-Drug Therapy), we have used the TD (Touch-Down) PCR. We arranged and amplified sequences of the genes, folP, rpoB, gyr, 23S rRNA, in M. leprae involved in MDT-resistance, and could obtain the PCR product each gene, simultaneously. This method, based on annealing temperature, was useful to the detection for diagnosis and the screen of MDT-resistant strain of M. leprae, rapidly. Thus, we suggest that the RLEP primer and TD-PCR method are effective in assessing the diagnosis of leprosy and the identification of drug-resistant M. leprae.
Diagnosis*
;
DNA
;
Leprosy*
;
Polymerase Chain Reaction*
;
Repetitive Sequences, Nucleic Acid
4.Effect of Premedication Method and Drug Resistance of Antiplatelet Agent on Periprocedural Thromboembolic Events During Coil Embolization of an Unruptured Intracranial Aneurysm.
Se Hwan PARK ; Yong Bae KIM ; Seung Kon HUH
Journal of Cerebrovascular and Endovascular Neurosurgery 2012;14(3):148-156
OBJECTIVE: A retrospective review of premedication method and drug resistance of aspirin and clopidogrel in association with thromboembolic events during and after coil embolization of an unruptured intracranial aneurysm was conducted. METHODS: Our premedication policy for coil embolization of an unruptured intracranial aneurysm has changed from administration of the loading dose before the procedure (i.e. loading group) to repeated administration of the maintenance dose for several days (i.e. preparation group). The loading group (27 patients with 29 aneurysms) and the preparation group (30 patients with 35 aneurysms) were compared for identification of the effect of premedication method on periprocedural thromboembolic events. The results of drug response assays of the preparation group were analyzed with respect to periprocedural thromboembolic events. RESULTS: No statistically significant difference in incidence of thromboembolic events was observed between the loading group and the preparation group. Analysis of the results of the drug response assay showed high prevalence (56.7%, 73.3%) of clopidogrel resistance and relatively low prevalence (6.7%) of aspirin resistance. Patients who had thromboembolic events tended to have lower responsiveness to both aspirin and clopidogrel than patients without it. CONCLUSION: The method of antiplatelet premedication does not affect the rate of periprocedural thromboembolic events in coil embolization for treatment of an unruptured intracranial aneurysm. Nevertheless, considering the high prevalence of drug resistance, it is reasonable to premedicate antiplatelet agents in the preparation method for the drug response assay. Use of a higher dose of aspirin and clopidogrel or addition of an alternative drug (cilostazol or triflusal) can be applied against antiplatelet agent resistance. However, because the hemorrhagic risk associated with this supplementary use of antiplatelet agent has not been well-documented, the hemorrhagic risk and the preventive benefit must be weighed.
Aspirin
;
Drug Resistance
;
Humans
;
Incidence
;
Intracranial Aneurysm
;
Platelet Aggregation Inhibitors
;
Premedication
;
Prevalence
;
Retrospective Studies
;
Ticlopidine
5.Rupture of De Novo Anterior Communicating Artery Aneurysm 8 Days after the Clipping of Ruptured Middle Cerebral Artery Aneurysm.
Sung Kon HA ; Dong Jun LIM ; Sang Dae KIM ; Se Hoon KIM
Journal of Korean Neurosurgical Society 2013;54(3):236-238
Rapidly developed de novo aneurysm is very rare. We present a rapidly developed and ruptured de novo anterior communicating aneurysm 8 days after the rupture of another aneurysm. This de novo aneurysm was not apparent in the initial 3-dimensional computed tomography and digital subtraction angiography. We reviewed the literature and discussed possible mechanisms for the development of this de novo aneurysm.
Aneurysm
;
Angiography, Digital Subtraction
;
Intracranial Aneurysm*
;
Middle Cerebral Artery*
;
Rupture*
;
Subarachnoid Hemorrhage
6.Discrepancy in T cell clonal expansions in synovial fluid and peripheral blood from rheumatoid arthritis patients.
In Hong CHOI ; Youngjoon CHWAE ; Soo Kon LEE ; Minkyung CHU ; Joo Deuk KIM ; Se Jong KIM
Yonsei Medical Journal 1995;36(1):68-76
Rheumatoid arthritis (RA) is an autoimmune disease involving the synovial membrane of peripheral joints. T cells specific for self antigens may play a critical role. Identification of T cell receptors (TCR) of such specific T cell clones is very important for treatment, prevention and identification of relevant autoantigens. To identify specific T cells, TCR V beta family repertoire and the clonal expansion of T cells were analyzed in this study. The percentage of V beta 5+ or V beta 8+ cells in the synovial fluid mononuclear cells (SFMCs) was similar to that in the peripheral blood mononuclear cells (PBMCs). However, the percentage of DR+ T cells in the SFMCs was higher (p< 0.01). Analyzing the clonality of T cells in 8 V beta families (V beta 1, V beta 5, V beta 8, V beta 14, V beta 16, V beta 17, V beta 18, V beta 20), clonal expansions in CD8+ T cells from the SFMCs were found more frequently than in the PBMCs. The patterns of clonal expansions were discrepant between the SFMCs and the PBMCs even in the same patient, which suggests several inflamed tissue specific T cell clonal expansions in the SFMCs. These T cell clones might be activated by autoantigens which are not identified yet and responsible for the RA pathogenesis.
Arthritis, Rheumatoid/*metabolism/pathology
;
Base Sequence
;
Blood Cells/*metabolism
;
Clone Cells
;
Female
;
Human
;
Male
;
Molecular Probes
;
Molecular Sequence Data
;
Polymerase Chain Reaction
;
Receptors, Antigen, T-Cell/genetics/*metabolism
;
Support, Non-U.S. Gov't
;
Synovial Fluid/cytology/*metabolism
;
T-Lymphocytes/*metabolism
7.Three cases of double primary lung cancer.
Yeong Sung KIM ; Jong Kon LEE ; Ok Sik SHIN ; Gyu Chang SHIN ; Byung Sam LEE ; Yong Ku OH ; Se Kil KEE ; In Mook CHO ; Byeong Hun KIM
Tuberculosis and Respiratory Diseases 1991;38(2):186-193
No abstract available.
Lung Neoplasms*
;
Lung*
8.Triple Primary Origin Tumor: A Case Report.
Yong Su JUNG ; Se Hoon KIM ; Sung Kon HA ; Sang Dae KIM ; Dong Jun LIM
Korean Journal of Spine 2013;10(2):91-93
Generally, among the extradural spinal tumors, metastatic spinal tumor is much more common than primary spinal tumors. Thus, in the case of a spinal tumor patient with cancer history (such as lung cancer, breast cancer, etc.), we used to infer that the spinal lesion is the metastasis from, primary malignancy. We introduce an experience of a case of triple primary origin tumor in a 57-year-old man. When the spinal lesion was found on the abdominal computed tomography scan, he already had a history of colon cancer and liver cancer. Initially, it was thought that the lesion would probably be a metastatic tumor from the liver or colon cancers, and the operation was performed accordingly. In the pathologic final report, however, the mass was proven to plasmacytoma - the third primary lesion. The patient underwent chemotherapy after surgery. Globally, the triple primary origin tumor has been reported very rarely. With this report, we wish to emphasize the necessity of pathologic confirmation and adequate treatment even in a patient with known malignancies.
Breast Neoplasms
;
Colonic Neoplasms
;
Humans
;
Liver
;
Liver Neoplasms
;
Lung Neoplasms
;
Neoplasm Metastasis
;
Plasmacytoma
;
Tetracyclines
9.Detection of point mutation at C-terminal region of phagosomal coat protein (TACO) in patients with leprosy.
Se Kon KIM ; Tae Jin KANG ; Byoung Chul KIM ; Gue Tae CHAE
Korean Leprosy Bulletin 2003;36(1):11-26
Mycobacteria, which are highly successful pathogen, resist delivary to lysosomes and instead survive within a specialized vacuole, the mycobacterial phagosome. The bacteria survive intracellularly because they are able to actively recruit and retain TACO ( tryptophane aspartate-containing coat protein ) at the mycobacterial phagosome, where it prevents lysosomal delivary in a cholesterol-dependent manner. In this study, we investigated the difference of TACO expression is whether related to mutant in coro1a gene in patients with leprosy and normal volunteer. First, we screened for detection of a mutant in the leucine zipper motif within the exon 11, and then in the exon 9 to 10, and finally in the coiled-coil region. Interestingly, single base substitutions ( point mutation ) presents at assembly site of U1 snRNP, around of 5' splice site in the intron 9, there are a C to T and G to A transition are at 9 bp and 14 bp downstream of 5' splice site, respectively, and both of it. Among the 3 types of polymorphism, frequency of a G to A transition is markedly increased in patients of lepromatous type, which are new cases or relapsed. Both a C to T and G to A transitions are found in 1 case of tuberculoid type and 2 cases in lepromatoue type, but not found in control group. The silent mutation in leucine zipper motif within the exon 11 is located at codon at 454 ( CTG-->CTA), which is 1st leucine from C-terminal among four leucine zipper. In coiled-coil region, no mutation is found in genomic DNA of patients with leprosy. Further, we will do functional study about the identified point mutation and will screen any possible mutation in the region of promotor and WD repeat.
Bacteria
;
Codon
;
DNA
;
Exons
;
Healthy Volunteers
;
Humans
;
Introns
;
Leprosy*
;
Leucine
;
Leucine Zippers
;
Lysosomes
;
Phagosomes
;
Point Mutation*
;
Ribonucleoprotein, U1 Small Nuclear
;
RNA Splice Sites
;
Tryptophan
;
Vacuoles
10.Fatal Case of Cerebral Aspergillosis : A Case Report and Literature Review.
Jae Chang LEE ; Dong Jun LIM ; Sung Kon HA ; Sang Dae KIM ; Se Hoon KIM
Journal of Korean Neurosurgical Society 2012;52(4):420-422
Cerebral aspergillosis is rare and usually misdiagnosed because its presentation is similar to that of a tumor. The correct diagnosis is usually made intra-operatively. Cerebral abscess with fungal infection is extremely rare and few cases have been reported, but it carries a poor prognosis. A 73 year-old man presented with decreased visual acuity and paresis of the right cranial nerve III. Magnetic resonance imaging (MRI) revealed a mass in the right cavernous sinus, extened to the anterior crainial fossa and the superior orbital fissure. During surgery, a well encapsulated pus pocket was found, and histopathological examination of the mass resulted in the diagnosis of aspergillosis. Despite appropriate anti-fungal treatment, the patient eventually died from fatal cerebral ischemic change and severe brain swelling. The correct diagnosis of cerebral aspergillosis can only be achieved by histopathological examination because clinical and radiological findings including MRI are not specific. Surgical intervention and antifungal therapy should be considered the optimal treatment. Early diagnosis and aggressive antifungal treatment provide good results.
Aspergillosis
;
Brain
;
Brain Abscess
;
Cavernous Sinus
;
Early Diagnosis
;
Humans
;
Magnetic Resonance Imaging
;
Neuroaspergillosis
;
Oculomotor Nerve
;
Orbit
;
Paresis
;
Pyrimidines
;
Suppuration
;
Triazoles
;
Visual Acuity