1.Treatment of refractory adult immune thrombocytopenic purpura with protein A-immunoadsorption.
Kyou Sup HAN ; Seon Yang PARK ; Byoung Kook KIM
Korean Journal of Blood Transfusion 1993;4(2):173-180
No abstract available.
Adult*
;
Humans
;
Purpura, Thrombocytopenic, Idiopathic*
2.Treatment of refractory adult immune thrombocytopenic purpura with protein A-immunoadsorption.
Kyou Sup HAN ; Seon Yang PARK ; Byoung Kook KIM
Korean Journal of Blood Transfusion 1993;4(2):173-180
No abstract available.
Adult*
;
Humans
;
Purpura, Thrombocytopenic, Idiopathic*
3.Peripheral Blood Stem Cell Collection with an Automated Blood Cell Separator.
Byoung Kook KIM ; Seon Yang PARK ; Kyou Sup HAN
Korean Journal of Blood Transfusion 1994;5(1):1-8
Peripheral blood stem cells(PBSC) were collected for autologous transplantation for the first time in Korea wish Fenwal CS-3000 Plus blood cell separator. Twenty-nine procedures were performed for 7 patients without any incidents. GM-CSF(400ug) was administered daily for 5 days before PBSC collection and the collections were performed 3-6 successive days. A total of 3.5-11.4 x 109 mononuclear cells(MNCs) were collected from 7,000mL blood processed per procedure. The number of MNCs collected was mainly dependent on the concentration of MNCs in patient's blood(r = 0.68, p<0.01). We concluded that the PBSC trans plantation program could be set up without difficulty in Korea since the Fenwal CS-3000 Plus blood cell separator is already available in many institutions and the procedure used in this study is easy to follow.
Autografts
;
Blood Cells*
;
Humans
;
Korea
;
Stem Cells*
;
Transplantation, Autologous
4.Platelet alloimmunization after multiple blood transfusions.
Kyou Sup HAN ; Sang In KIM ; Byoung Kook KIM ; Seon Yang PARK ; Young Chul OH
Korean Journal of Blood Transfusion 1991;2(1):19-27
No abstract available.
Blood Platelets*
;
Blood Transfusion*
5.Species-Specific Detection of Listeria monocytogenes by Polymerase Chain Reaction.
Byoung Seon YANG ; Jin Sook PARK
Journal of the Korean Society for Microbiology 1997;32(2):213-218
Three Listeria monocytogenes strains isolated from clinical cerebrospinal fluid samples. A PCR was performed by using oligonuclotide primers derived from the invasion-associated protein(iap) related gene sequence. As a result of PCR, we obtained 287-bp DNA fragment of specific product to L. monocytogenes species. The chromsomal DNA of genera Listeria species were subjected to southern blot hybridization with HRP-labeled 287-bp DNA probe to produce a L. monocytogenes banding pattern. In the cases of 10-fold dilution of L. monocytogenes cells, 8 x 10(2) cells/ml were detected by PCR.
Blotting, Southern
;
Cerebrospinal Fluid
;
DNA
;
Listeria monocytogenes*
;
Listeria*
;
Polymerase Chain Reaction*
6.Histological classification of chronic myelogenous leukemia : clinicopathologic correlation and prognostic significance.
Nam Yong LEE ; Sung Sup PARK ; Han Ik CHO ; Sang In KIM ; Byoung Kook KIM ; Seon Yang PARK ; Heon KIM
Korean Journal of Clinical Pathology 1993;13(2):197-209
No abstract available.
Classification*
;
Leukemia, Myelogenous, Chronic, BCR-ABL Positive*
7.Combination chemotherapy with cytosine arabinoside and idarubicin for acute myelogenous leukemia.
Hyun Choon SHIN ; Chul Won JUNG ; Jin Hak LEE ; Jung Ae LEE ; Sung Hyun YANG ; Young Hyuk LEEM ; Seon Yang PARK ; Byoung Kook KIM ; Noe Kyoung KIM
Korean Journal of Hematology 1993;28(2):247-255
No abstract available.
Cytarabine*
;
Cytosine*
;
Drug Therapy, Combination*
;
Idarubicin*
;
Leukemia, Myeloid, Acute*
8.Peripheral T - cell Lymphomas Presenting as Fever of Unknown Origin.
Dae Seog HEO ; Keun Seok LEE ; Joor Yung HUH ; Yung Jue BANG ; Seon Yang PARK ; Chul Woo KIM ; Byoung Kook KIM ; Noe Kyeong KIM
Journal of the Korean Cancer Association 1998;30(2):329-337
PURPOSE: Peripheral T-cell lymphomas(PTCL) show diverse clinical and histological characteristics and should be understood as mixtures of heterogeneous entities. Although many clinical and biological parameters have been proposed for classifying PTCL into different prognostic groups, few parameters have turned out to be appropriate for classification. To investigate the clinical significance of FUO presentation in PTCL, comparisons of clinical parameters were performed using non-FUO presentation as a control. MATERIALS AND METHODS: 66 cases of Korean PTCL were divided into FUO group and non-FUO group according to the presentation and compared with each other. RESULTS: Among 66 patients of PTCL, 19 patients presented with FUO. Compared with non-FUO group, FUO group showed no significant age and sex ratio differences. FUO group showed more advanced stage, worse performance status than non-FUO group. Predominant sites of definite diagnosis were skin, gastrointestinal tract and liver in FUO group and nasal cavity and paranasal sinus in non-FUO group. There were no significant differences between histologic classifications of both groups. Survival analysis revealed significant differences between both groups. FUO group showed significantly shorter survival. Prognostic factor analysis(multivariate) was done with stage, LDH level, performance status, and FUO status. FUO status, stage and performance status were significant determinants of survival, but LDH level proved to have no prognostic implication. CONCLUSION: PTCL with FUO presentation showed such distinct characteristics that the authors propose fever of unknown origin(FUO) as a clinical parameter for classifying PTCL. Further studies are needed to identify biological parameters which characterize PTCL with FUO presentation.
Classification
;
Diagnosis
;
Fever of Unknown Origin*
;
Fever*
;
Gastrointestinal Tract
;
Humans
;
Liver
;
Lymphoma*
;
Nasal Cavity
;
Prognosis
;
Sex Ratio
;
Skin
;
T-Lymphocytes
9.Combination chemotherapy with vincristine, melphalan and prednisone for multiple myeloma.
Tae You KIM ; Dae Seog HEO ; Yung Jue BANG ; Seon Yang PARK ; Byoung Kook KIM ; Noe Kyeong KIM ; Hyo Jin KIM
Korean Journal of Medicine 1993;45(1):1-11
No abstract available.
Drug Therapy, Combination*
;
Melphalan*
;
Multiple Myeloma*
;
Prednisone*
;
Vincristine*
10.Cell Cycle Analysis by Ki-67 Monoclonal Antibody in Acute Myelogenous Leukemia.
Jin Seok AHN ; Eun Shil KIM ; Heung Tae KIM ; Seon Yang PARK ; Byoung Kook KIM
Korean Journal of Hematology 2002;37(3):191-199
BACKGROUND: Flow cytometric measurement of DNA can reveal G0/G1, S, G2/M phases of cell cycle, and BrdU labeling can determine the percentage of cells in active DNA synthesis. A monoclonal antibody (MoAb), Ki-67, recognizes a protein that is present only in the nucleus of cycling cells but absent in resting cells. We analyzed whether the resting and the proliferating fraction could be differentiated by double staining with Ki-67 MoAb and propidium iodide (PI), and observed the effects of GM-CSF on cell cycle in acute myelogenous leukemia (AML) cells by Ki-67 MoAb. METHODS: Blast cells were prepared from 9 AML patients. The cells were incubated for 48 hours with or without GM-CSF. Cells were stained with BrdU/PI and Ki-67/PI. Cell cycle was analyzed by flow cytometry. RESULTS: The average fraction of G0/G1, S, and G2/M phases was 84.6%, 10.9%, and 4.5 % by BrdU/PI and 87.8%, 8.6%, and 3.7% by Ki-67/PI, respectively. Ki-67/PI staining dis-criminated between G0 and G1 phases and the average was 71.5% and 16.3%, respectively. In cells incubated with GM-CSF, BrdU/ PI method showed that the average S phase fraction (SPF) significantly increased from 10.9 to 16.2% (P=0.01) and the fraction of G0/G1 phase decreased from 84.6% to 78.4% (P= .02). Ki-67/PI method showed that the median SPF significantly increased from 8.6% to 13.7% (P=0.05) and G0 fraction decreased from 71.5% to 58.1% (P=0.02) but G1 fraction increased from 16.3% to 22.3% (P=0.01). CONCLUSION: Cell cycle analysis by Ki-67 MoAb and PI in AML is rapid and simple. It is especially useful to determine the growth fraction and G0 fraction compared to BrdU/PI staining.
Bromodeoxyuridine
;
Cell Cycle*
;
DNA
;
Flow Cytometry
;
G0 Phase
;
G1 Phase
;
Granulocyte-Macrophage Colony-Stimulating Factor
;
Humans
;
Ki-67 Antigen
;
Leukemia, Myeloid, Acute*
;
Propidium
;
S Phase