Primary bone marrow diffuse large B cell lymphoma: a case series and review

被引:38
作者
Chang, Hung [1 ,2 ]
Hung, Yu-Shin [1 ,2 ]
Lin, Tung-Liang [1 ,2 ]
Wang, Po-Nan [1 ,2 ]
Kuo, Ming-Chung [1 ,2 ]
Tang, Tzung-Chih [1 ,2 ]
Wu, Jin-Hou [1 ,2 ]
Dunn, Po [1 ,2 ]
Shih, Lee-Yung [1 ,2 ]
机构
[1] Chang Gung Mem Hosp, Div Hematol Oncol, Taipei 10591, Taiwan
[2] Chang Gung Univ, Sch Med, Tao Yuan, Taiwan
关键词
Diffuse large B cell lymphoma; Bone marrow; Rituximab; CD5; CD5(+); INVOLVEMENT;
D O I
10.1007/s00277-010-1129-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diffuse large cell lymphoma involving bone marrow is not uncommon, but primary, de novo, bone marrow diffuse large B cell lymphoma (DLBCL) is rare. To understand the clinical features and outcomes of this distinct entity, we collected 12 cases in 5 years from a single-center database. They accounted for 1.16% of lymphoma, or 2.65% of diffuse large B cell lymphoma. Nine cases presented with fever of unknown origin. Lactate dehydrogenase levels were elevated in all but one case. Nine cases belonged to the high-risk group according to their international prognosis indexes (score 4 or 5). Four patients received no chemotherapy, all of whom died within 1 month. Four patients received cyclophosphamide, adriamycin, vincristine, and prednisolone (CHOP)-like chemotherapy, and their median survival was 13 months. Finally, four patients received rituximab 375 mg/m(2) in addition to CHOP-like chemotherapy. All of them had complete remission and three are still alive without relapse. We concluded that primary bone marrow DLBCL is a rare but distinctive subtype of lymphoma. The prognosis for this entity is poor but rituximab-based treatment is promising for improving its outcomes.
引用
收藏
页码:791 / 796
页数:6
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