Composite T lymphoblastic leukemia/lymphoma and diffuse large B-cell lymphoma: Case report

被引:6
|
作者
Niino, Daisuke [1 ]
Ohsaki, Koichi [2 ]
Arakawa, Fumiko [1 ]
Watanabe, Jiro [3 ]
Kimura, Yoshizo [1 ]
Kiyasu, Junichi [1 ]
Takeuchi, Masanori [1 ]
Miyoshi, Hiroaki [1 ]
Yoshida, Maki [1 ]
Sugita, Yasuo [1 ]
Ohshima, Koichi [1 ]
Okamura, Takashi [2 ]
机构
[1] Kurume Univ, Sch Med, Dept Pathol, Kurume, Fukuoka 8300011, Japan
[2] Kurume Univ, Sch Med, Div Hematol, Kurume, Fukuoka 8300011, Japan
[3] Yame Gen Hosp, Dept Pathol, Fukuoka, Japan
关键词
composite lymphoma; diffuse large B-cell lymphoma; lymphoblastic leukemia; lymphoma; NON-HODGKINS-LYMPHOMA; LYMPHOPROLIFERATIVE DISORDERS; DISEASE; LEUKEMIA; PATIENT; NODE; EBV;
D O I
10.1111/j.1440-1827.2011.02662.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
This report concerns a unique case of a composite lymphoma composed of T-lymphoblastic leukemia/lymphoma (T-LBL) and diffuse large B-cell lymphoma (DLBCL) in a 72-year-old woman with generalized lymphadenopathy, splenomegaly and ascites. Laboratory findings showed increased lactate dehydrogenase and soluble interleukin-2 receptor. The biopsy specimen showed replacement of the normal architecture of the lymph nodes by a tumor containing a dual cell population composed of large lymphocytes and medium-sized lymphocytes. Sheets of large lymphocytes often were punctuated by clusters of medium-sized lymphocytes. Flow cytometry and immunohistochemical analysis showed a composite lymphoma with both T-LBL and DLBCL. The T-LBL expressed CD1a, CD3, CD4, CD8, and terminal deoxynucleotidyl transferase. The DLBCL expressed CD19 and CD20, CD23, bcl-2, bcl-6, MUM1 and immunoglobulin kappa light chain. Polymerase chain reaction detected a monoclonal pattern of T-cell receptor gamma and immunoglobulin heavy chain rearrangements in the same specimen. She received eight cycles of R-CHOP (rituximab+cyclophosphamide, doxorubicin, vincristine, prednisone) therapy and achieved complete remission. She has shown no signs of recurrence 20 months after the diagnosis. We describe here a very unusual and, to the best of our knowledge, an as yet never reported case of a primary composite lymphoma of T-LBL and DLBCL.
引用
收藏
页码:363 / 368
页数:6
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