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NCCN 指南解读:T 细胞淋巴瘤,第 1.2021 版。

NCCN Guidelines Insights: T-Cell Lymphomas, Version 1.2021.

机构信息

1Memorial Sloan Kettering Cancer Center.

2Mayo Clinic Cancer Center.

出版信息

J Natl Compr Canc Netw. 2020 Nov 2;18(11):1460-1467. doi: 10.6004/jnccn.2020.0053.

Abstract

Hepatosplenic T-cell lymphoma (HSTCL) is a rare subtype of T-cell lymphoma associated with an aggressive clinical course and a worse prognosis. HSTCL develops in the setting of chronic immune suppression or immune dysregulation in up to 20% of cases and is most often characterized by spleen, liver, and bone marrow involvement. Diagnosis and management of HSTCL pose significant challenges given the rarity of the disease along with the absence of lymphadenopathy and poor outcome with conventional chemotherapy regimens. These Guidelines Insights focus on the diagnosis and treatment of HSTCL as outlined in the NCCN Guidelines for T-Cell Lymphomas.

摘要

肝脾 T 细胞淋巴瘤(HSTCL)是一种罕见的 T 细胞淋巴瘤亚型,与侵袭性临床病程和预后较差相关。高达 20%的病例中,HSTCL 在慢性免疫抑制或免疫失调的背景下发生,最常表现为脾脏、肝脏和骨髓受累。由于该疾病罕见,且缺乏淋巴结病,以及传统化疗方案的预后不良,HSTCL 的诊断和管理带来了重大挑战。这些指南要点重点关注 NCCN T 细胞淋巴瘤指南中概述的 HSTCL 的诊断和治疗。

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