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病例报告:一例外周T细胞淋巴瘤(NOS)的流式细胞术鉴别诊断,其CD45完全缺失且CD3呈弱阳性表达

Case Report: Flow cytometric differential diagnosis of a peripheral T-cell lymphoma, NOS with complete loss of CD45 and dim expression of CD3.

作者信息

Szalóki Gábor, Szepesi Ágota, Tárkányi Ilona, Márk Ágnes, Kriston Csilla, Hunyadi Anna, Mózes Réka, Barna Gábor

机构信息

Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.

Department of Internal Medicine and Haematology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.

出版信息

Pathol Oncol Res. 2025 May 29;31:1612095. doi: 10.3389/pore.2025.1612095. eCollection 2025.

Abstract

Peripheral T-cell lymphomas (PTCLs) are a group of non-Hodgkin lymphomas originating from mature T-lymphocytes. Despite encompassing several well-defined entities, about 25% of the PTCLs do not fulfill the requirements of any of the subcategories. These diseases are classified as PTCL, not otherwise specified (PTCL, NOS), and often associated with poor prognosis. Hereby we present a case of a female patient, diagnosed with PTCL, NOS from her skin biopsy specimen. Besides histology and immunohistochemistry, flow cytometry was used for phenotyping and staging (peripheral blood, bone marrow). Pathologic T-cells were found in all the investigated tissues, with a very unusual CD45 negative and surface CD3 dim immunophenotype. For proper differential diagnosis, we determined several markers with immunohistochemistry (CD3, CD4, CD7, CD8, CD30, PD1, Ki-67) and flow cytometry: (CD2, cytoplasmic CD3, surface CD3, CD4, CD5, CD7, CD8, CD9, CD10, CD19, CD20, CD26, CD34, CD38, CD45, CD48, CD56, CD99, CD123, surface TRBC1, cytosplasmic TRBC1, surface TRBC2, cytoplasmic TRBC2, MPO, TdT, Igκ, Igλ). Here we discuss the difficulties of the differential diagnostic process and highlight some potential pitfalls of flow cytometric analysis of the pathologic T-cells with such a rare immunophenotype. Despite several determined markers, the disease characteristics did not meet the criteria of any PTCL subtype, therefore the diagnosis remained PTCL, NOS. Due to the aggressive course of the disease, we lost the patient within 1 year after the diagnosis.

摘要

外周T细胞淋巴瘤(PTCL)是一组起源于成熟T淋巴细胞的非霍奇金淋巴瘤。尽管包含几个明确的实体,但约25%的PTCL不符合任何亚类的标准。这些疾病被归类为外周T细胞淋巴瘤,非特指型(PTCL,NOS),且通常预后较差。在此,我们报告一例女性患者,其皮肤活检标本诊断为PTCL,NOS。除了组织学和免疫组织化学检查外,还采用流式细胞术进行表型分析和分期(外周血、骨髓)。在所有研究组织中均发现了病理性T细胞,其免疫表型非常罕见,CD45阴性且表面CD3弱阳性。为了进行准确的鉴别诊断,我们通过免疫组织化学(CD3、CD4、CD7、CD8、CD30、PD1、Ki-67)和流式细胞术检测了几种标志物:(CD2、胞质CD3、表面CD3、CD4、CD5、CD7、CD8、CD9、CD10、CD19、CD20、CD26、CD34、CD38、CD45、CD48、CD56、CD99、CD123、表面TRBC1、胞质TRBC1、表面TRBC2、胞质TRBC2、MPO、TdT、Igκ、Igλ)。在此,我们讨论鉴别诊断过程中的困难,并强调对具有这种罕见免疫表型的病理性T细胞进行流式细胞术分析时的一些潜在陷阱。尽管检测了多种标志物,但该疾病特征不符合任何PTCL亚型的标准,因此诊断仍为PTCL,NOS。由于疾病进展迅速,患者在诊断后1年内死亡。

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