涉及肝细胞癌的懒惰T淋巴细胞增生--新情况下的表现及文献综述。

Pub Date : 2023-09-01 Epub Date: 2023-07-16 DOI:10.1007/s12308-023-00554-7
Alireza Ghezavati, Christine A Liang, Daniel Mais, Alia Nazarullah
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引用次数: 0

摘要

隐匿性T淋巴细胞增生(iT-LBP)是一种罕见的、非克隆性、鞘外淋巴细胞增生,具有未成熟T细胞表型、临床过程隐匿、预后良好等特点。虽然其发病机制尚不清楚,但有报道称它们与 Castleman 病、滤泡树突状细胞瘤/肉瘤、血管免疫母细胞性 T 细胞淋巴瘤、肝细胞癌(HCC)、重症肌无力和尖细胞癌有关。文献中报道的 iT-LBP 病例约有 51 例。由于该病与一种侵袭性恶性肿瘤--急性T细胞白血病/淋巴瘤(T-ALL)具有相同的形态学和免疫表型特征,因此识别和准确诊断该病至关重要。肝移植后和转移部位的 HCC 中出现 IT-LBP 的文献尚未见报道。本文描述了两例肝移植后复发和转移性 HCC 患者的病例报告。一名 50 岁的男性患者患有伴有 HCC 的终末期肝病,接受了肝移植。一年后,他出现了肺转移,并伴有 iT-LBP。一名 69 岁的男子因终末期肝病和 HCC 接受了肝移植手术。两名患者的 iT-LBP 均表达 TdT、CD3 和 CD4,缺乏 CD34 和克隆 T 细胞受体基因重排。经回顾性复查,移植前的 HCC 标本缺乏 iT-LBP。我们介绍了两例与 HCC 相关的 iT-LBP 新病例--肝移植后患者和 HCC 复发/转移部位。此外,我们还对已报道的 iT-LBP 病例的临床、组织学和免疫表型特征进行了全面的文献综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Indolent T-lymphoblastic proliferation involving hepatocellular carcinoma-presentation in novel settings and comprehensive review of literature.

Indolent T-lymphoblastic proliferation (iT-LBP) is a rare, non-clonal, extrathymic lymphoid proliferation with an immature T cell phenotype, indolent clinical course, and excellent prognosis. Although their pathogenesis is unclear, they are reported to be associated with Castleman disease, follicular dendritic cell tumors/sarcomas, angioimmunoblastic T cell lymphoma, hepatocellular carcinoma (HCC), myasthenia gravis, and acinic cell carcinoma. There are around 51 reported cases of iT-LBP in the literature. Recognition and accurate diagnosis of this entity is critical as it shares morphologic and immunophenotypic features with an aggressive malignancy-acute T cell leukemia/lymphoma (T-ALL). IT-LBP in HCC post-liver transplant and in metastatic sites has not been reported in the literature. Two case reports of patients presenting with recurrent and metastatic HCC in post-liver transplant settings are described. A 50-year-old man with an end-stage liver disease with HCC underwent liver transplant. A year later, he developed pulmonary metastasis with associated iT-LBP. A 69-year-old man underwent liver transplant for end-stage liver disease and HCC. Eighteen months later, he developed recurrent HCC in the transplanted liver and omental metastasis; both sites showed HCC with iT-LBP. iT-LBP in both patients expressed TdT, CD3, and CD4 and lacked CD34 and clonal T cell receptor gene rearrangements. On retrospective review, the pre-transplant HCC specimens lacked iT-LBP. We present two cases of iT-LBP associated with HCC in novel settings-in post-liver transplant patients and in recurrent/metastatic sites of HCC. In addition, a comprehensive literature review of clinical, histological, and immunophenotypic characteristics of reported cases of iT-LBP is presented.

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