1.Clinical Significance of Membrane CD22 in B-lineage Acute Lymphoblastic Leukemia.
Korean Journal of Clinical Pathology 1999;19(3):337-341
BACKGROUND: CD22 is a glycoprotein expressed on the surface of normal mature B cells and in the cytoplasm of normal B cell precursors. Cytoplasmic CD22 (cCD22) has been proposed as a immunologic marker for the diagnosis of B-lineage acute lymphoblastic leukemia (ALL) while membrane CD22 (mCD22) has been used as the marker for chronic lymphocytic leukemia, B-lineage lymphoma, and hairly cell leukemia, and mCD22 has not been routinely used for the diagnosis and subgrouping of ALL. The purpose of this study was to examine the expression of mCD22 in B-lineage ALL and its clinical significance. METHODS: From 1992 to April, 1998, the leukemic cells of 64 patients newly diagnosed as B-lineage ALL by immunophenotyping were analyzed by the direct immunofluorescence method using monoclonal antibodies including mCD22. RESULTS: mCD22 was positive in 53% (34/64) of all patients, 50% (21/42) of children and 59% (13/22) of adults. According to the immunologic classification, mCD22 was positive in 44% (4/9) of group II, 53% (19/36) of group III, 69% (11/16) of group IV, but negative in 3 cases of group V and VI. The complete remission rate of the mCD22 negative group in group III was significantly higher than that of the mCD22 positive group (P=0.008). There were significant differences in survival rates between the mCD22 positive group and the mCD22 negative group in group II, III and IV (P=0.046) and the above observed significant difference was seen when group III was separately tested (P=0.014). CONCLUSIONS: Our study demonstrated that the expression of mCD22 may be a poor prognostic factor in B-lineage ALL and that mCD22 shall be clinically used as a prognostic marker especially in group III, which is most common among the subgroups of B-lineage ALL.
Adult
;
Antibodies, Monoclonal
;
B-Lymphocytes
;
Biomarkers
;
Child
;
Classification
;
Cytoplasm
;
Diagnosis
;
Fluorescent Antibody Technique, Direct
;
Glycoproteins
;
Humans
;
Immunophenotyping
;
Leukemia
;
Leukemia, Lymphocytic, Chronic, B-Cell
;
Lymphoma
;
Membranes*
;
Precursor Cell Lymphoblastic Leukemia-Lymphoma*
;
Prognosis
;
Survival Rate
3.Furuncular Myiasis in a Traveler Returning from South America.
Jaeyoung SHIN ; Jong Hyun KIM ; You Chan KIM
Korean Journal of Dermatology 2012;50(7):662-663
No abstract available.
Myiasis
;
South America
4.Preliminary Study of Vaginal Cones:A conservative Method of Treating Stress Incontinence.
You Sik LEE ; Jong Hyun KIM ; Ju Tae SEO
Journal of the Korean Continence Society 1997;1(1):60-60
No abstract available.
6.Comparison of pregnancy rate after tubal anastomosis according to the menstrual cycle.
Seong Hye KIM ; Jong Ha PARK ; Young Chul YOU ; Hung Jong LEE ; Jong In KIM ; Du Ryong LEE
Korean Journal of Obstetrics and Gynecology 1993;36(7):1978-1986
No abstract available.
Female
;
Menstrual Cycle*
;
Pregnancy Rate*
;
Pregnancy*
7.Three demensional computed tomography in oral and maxillofacialregion.
Jong Won KIM ; Byeong Rin KIM ; Taek Kyoung KIM ; Jun Yoang YOU
Journal of the Korean Association of Oral and Maxillofacial Surgeons 1991;17(1):1-9
No abstract available.
8.Surgical decompression of thyrotoxic exophthalmos: a case report.
Hyeon Ok KIM ; Seong Hoon JEONG ; Seong Jong YOU ; Sung Soo KIM
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1993;20(4):849-858
No abstract available.
Decompression, Surgical*
;
Exophthalmos*
9.Consenital blepharophimosis with family history.
Hyeon Ok KIM ; Kwang Ho LEE ; Sung Moon CHUNG ; Seong Jong YOU ; Sung Soo KIM
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1993;20(5):1058-1063
No abstract available.
Blepharophimosis*
;
Humans
10.A study of effect on human epithelization by topical application of epidermal growth factor.
Hyeon Ok KIM ; Sung Moon CHUNG ; Seong Jong YOU ; Sung Soo KIM
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1993;20(3):509-518
No abstract available.
Epidermal Growth Factor*
;
Humans*