Korean J Hematol 2009; 44(3):
Published online September 30, 2009
https://doi.org/10.5045/kjh.2009.44.3.139
© The Korean Society of Hematology
송성헌 정승민 황덕원 최지영 유기덕 홍현석 안용우 노영욱 이지선 박병배 최정혜 김인순 이웅수 이영열
한양대학교 의과대학 내과학교실,진단검사의학교실
T cell large granular lymphocytic leukemia (T-LGL leukemia) is defined as a clonal proliferative disorder of CD3+ cytotoxic T cells. T-LGL leukemia usually expresses CD3+, CD4-, CD8+, CD16+, CD56- and CD57+ cell markers, and this represents a rearrangement of the T cell receptor (TCR) gene. The clinical course is indolent in most cases, but on rare occasions, when CD3+ and CD56+ are expressed on the leukemic cells, it can be more aggressive. We experienced a patient with T-LGL leukemia and the disease was indolent at the time of diagnosis, and so any specific treatment was not required. Two years after the initial diagnosis, her clinical course became quite aggressive as the CD 56+ cell surface antigen was expressed. We report here on the first case of T-LGL leukemia in Korea and we review the relevant literature. (Korean J Hematol 2009;44:139-143.)
Keywords T-cell large granular lymphocytic leukemia, CD56 antigen, CD3 antigen, Rheumatoid arthritis
Korean J Hematol 2009; 44(3): 139-143
Published online September 30, 2009 https://doi.org/10.5045/kjh.2009.44.3.139
Copyright © The Korean Society of Hematology.
송성헌 정승민 황덕원 최지영 유기덕 홍현석 안용우 노영욱 이지선 박병배 최정혜 김인순 이웅수 이영열
한양대학교 의과대학 내과학교실,진단검사의학교실
Sung Heon Song, Seong Min Chung, Deok Won Hwang, Ji Young Choi, Ki Deok Yoo, Hyun Seok Hong, Yong Woo Ahn, Young Wook Roh, Ji Sun Lee, Byoung Bae Park, Jung Hye Choi, In Soon Kim, Woong Soo Lee, Young Yiul Lee
Departments of Internal Medicine, Clinical Pathology, College of Medicine, Hanyang University, Seoul, Korea
T cell large granular lymphocytic leukemia (T-LGL leukemia) is defined as a clonal proliferative disorder of CD3+ cytotoxic T cells. T-LGL leukemia usually expresses CD3+, CD4-, CD8+, CD16+, CD56- and CD57+ cell markers, and this represents a rearrangement of the T cell receptor (TCR) gene. The clinical course is indolent in most cases, but on rare occasions, when CD3+ and CD56+ are expressed on the leukemic cells, it can be more aggressive. We experienced a patient with T-LGL leukemia and the disease was indolent at the time of diagnosis, and so any specific treatment was not required. Two years after the initial diagnosis, her clinical course became quite aggressive as the CD 56+ cell surface antigen was expressed. We report here on the first case of T-LGL leukemia in Korea and we review the relevant literature. (Korean J Hematol 2009;44:139-143.)
Keywords: T-cell large granular lymphocytic leukemia, CD56 antigen, CD3 antigen, Rheumatoid arthritis