Farcet J P, Gaulard P, Marolleau J P, Le Couedic J P, Henni T, Gourdin M F, Divine M, Haioun C, Zafrani S, Goossens M
INSERM U91, Département d'Enseignement, Hôpital Henri Mondor, Créteil, France.
Blood. 1990 Jun 1;75(11):2213-9.
Peripheral T-cell lymphomas consist of a clinically heterogeneous group of malignant disorders whose immunophenotype usually corresponds to that of normal mature T cells. We describe and correlate the clinical, histopathologic, phenotypic, and genotypic findings in two patients with malignant lymphoma presenting with hepatosplenic disease. The morphologic pattern of lymphoma was that of a sinusal/sinusoidal infiltration in spleen, marrow, and liver. This morphologic characteristic was associated with the presence of a productive clonal rearrangement of the T-cell receptor (TCR) delta gene. Lymphoma cells expressed a CD3-TCR-gamma delta- phenotype. They were also double negative (ie, CD4-CD8-) and lacked the CD5 and CD7 antigens. In one patient, tumor progression was associated with phenotypic changes that resulted in a CD3-TCR-gamma delta- phenotype with the same delta-gene rearrangement as initially. These observations suggest the existence of a new type of peripheral T-cell lymphoma characterized by its hepatosplenic presentation, and by the sinusal/sinusoidal tropism and the TCR-gamma delta phenotype of the malignant cells.
外周 T 细胞淋巴瘤由一组临床异质性的恶性疾病组成,其免疫表型通常与正常成熟 T 细胞的免疫表型相对应。我们描述并关联了两名表现为肝脾疾病的恶性淋巴瘤患者的临床、组织病理学、表型和基因特征。淋巴瘤的形态学模式为脾脏、骨髓和肝脏中的窦状/窦样浸润。这种形态学特征与 T 细胞受体(TCR)δ基因的有功能的克隆重排的存在相关。淋巴瘤细胞表达 CD3-TCR-γδ-表型。它们也是双阴性(即 CD4-CD8-),并且缺乏 CD5 和 CD7 抗原。在一名患者中,肿瘤进展与表型变化相关,导致出现与最初相同的δ基因重排的 CD3-TCR-γδ-表型。这些观察结果提示存在一种新型外周 T 细胞淋巴瘤,其特征为肝脾表现、恶性细胞的窦状/窦样嗜性以及 TCR-γδ表型。