Aggressive cutaneous T-cell lymphomas after TNFα blockade

被引:70
作者
Adams, AE
Zwicker, J
Curiel, C
Kadin, ME
Falchuk, KR
Drews, R
Kupper, TS
机构
[1] Harvard Univ, Sch Med, Dept Dermatol, Brigham & Womens Hosp, Cambridge, MA 02138 USA
[2] Dana Farber Canc Inst, Boston, MA USA
[3] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Cambridge, MA 02138 USA
[4] Beth Israel Deaconess Med Ctr, Div Hematol Oncol, Dept Med, Boston, MA USA
[5] Beth Israel Deaconess Med Ctr, Div Gastroenterol, Dept Med, Boston, MA USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.jaad.2004.03.047
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Pharmacologic blockade of TNFalpha has been a highly effective approach to treating several immunologically mediated diseases, including rheumatoid arthritis, Crohn's disease, and psoriatic arthritis.(1,2,3) Both etanercept, the recombinant extracellular domain of the tumor necrosis factor receptor 2 (TNFR2), and infliximab, a humanized murine antibody, bind TNFalpha and block its interaction with cell surface receptors. Recently, it has become clear that blockade of TNFalpha action is profoundly immunosuppressive, and may result in reactivation of tuberculosis and histoplasmosis, as well as the emergence of B-cell lymphomas.(4,5,6) In this report, we describe two cases of cutaneous and systemic T-cell lymphoma that progressed rapidly in the setting of TNFalpha blockade. Both cases were characterized by rapid onset, a fulminant clinical course with extensive cutaneous and systemic involvement, and death within months of diagnosis.
引用
收藏
页码:660 / 662
页数:3
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