Department of Pathology and Neuropathology, University Hospital and Comprehensive Cancer Center Tuebingen, Tuebingen, Germany.
Department of Internal Medicine II, Hematology, Oncology, Clinical Immunology and Rheumatology, University Hospital Tuebingen, Tuebingen, Germany.
Br J Haematol. 2024 May;204(5):2071-2076. doi: 10.1111/bjh.19335. Epub 2024 Feb 7.
Recent studies have shown that follicular helper T-cell lymphoma of angioimmunoblastic type (AITL), the most common nodal peripheral T-cell lymphoma (PTCL), frequently arises in a background of clonal haematopoiesis (CH), a preneoplastic condition affecting up to 40% of elderly individuals. Data on a potential CH association are limited for other PTCL. We report a unique patient who sequentially developed both cytotoxic PTCL, not otherwise specified and AITL with distinct T-cell receptor rearrangements but shared somatic mutations originating from the same CH clone, thus providing convincing evidence that CH can give rise to T-cell neoplasms of different lineage.
最近的研究表明,滤泡辅助 T 细胞淋巴瘤(AITL)是最常见的结外 T 细胞淋巴瘤(PTCL),它常发生在克隆性造血(CH)的背景下,这种前肿瘤状态影响高达 40%的老年人群。其他 PTCL 的 CH 相关性数据有限。我们报告了一个独特的患者,他先后发展出了两种不同的 T 细胞肿瘤,一种是非特指的细胞毒性 T 细胞淋巴瘤,另一种是 AITL,它们具有不同的 T 细胞受体重排,但具有相同 CH 克隆起源的共享体细胞突变,因此提供了令人信服的证据,证明 CH 可以引发不同谱系的 T 细胞肿瘤。