4.2 Review

Hepatosplenic γδ T-cell Lymphoma: An Overview

期刊

CLINICAL LYMPHOMA MYELOMA & LEUKEMIA
卷 13, 期 4, 页码 360-369

出版社

CIG MEDIA GROUP, LP
DOI: 10.1016/j.clml.2013.03.011

关键词

Allogeneic transplantation; Autologous transplantation; CHOP; Hyper-CVAD; T-cell receptor; TCR

向作者/读者索取更多资源

Peripheral T-cell lymphomas are a heterogeneous group of lymphoid malignancies. Among these, hepatosplenic gamma delta T-cell lymphoma (HTCL) represents an aggressive and treatment-resistant subgroup for which new avenues of treatment are critically needed. HTCL is characterized by primary extranodal distribution of the malignant cells with typical intrasinusoidal infiltration of the liver, spleen, and bone marrow, which results in hepatosplenomegaly and peripheral blood cytopenias. Another characteristic feature is the expression of gamma delta T-cell receptors. HTCL exhibits a rapid progressive course and an extremely poor response to currently known therapeutic strategies, with a 5-year overall survival rate of only 7%. In this review, we discuss the clinical, pathologic, and molecular characteristics of this disease, along with the challenges that are associated with its diagnosis and treatment. (C) 2013 Elsevier Inc. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据