Laboratoire d'Hématologie Cellulaire Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Lyon.
Haematologica. 2010 Apr;95(4):604-12. doi: 10.3324/haematol.2009.011049. Epub 2009 Dec 16.
Classically, splenic marginal zone B-cell lymphoma is characterized by the absence of CD5 expression. Cases of apparent splenic marginal zone B-cell lymphoma showing CD5 expression, as diagnosed by blood studies, have been described; however, in the absence of histological evidence, the correct diagnosis of these cases is controversial because of possible confusion with other CD5-positive small B-cell neoplasms.
We report a series of 24 CD5-positive, t(11;14)-negative cases of splenic marginal zone B-cell lymphoma diagnosed by flow cytometry studies of blood and histologically proven on spleen sections. Clinical data as well as morphological, immunological, cytogenetic and molecular characteristics were assessed to evaluate the similarities and differences of these cases with those of classical CD5-negative splenic marginal zone B-cell lymphoma.
The CD5 expression detected in blood by flow cytometry was confirmed in most cases by immunohistochemistry on spleen sections. In general, cases of CD5-positive and CD5-negative splenic marginal zone B-cell lymphoma did not appear different and, in particular, they showed similar karyotypic changes such as 7q deletion, trisomy 3, trisomy 18 and biased IGHV usage (i.e. VH1-2). The main differences were a higher lymphocyte count at diagnosis (8.15x10(9)/L versus 3.90x10(9)/L; P=0.005) and more frequent diffuse bone marrow infiltration (34% versus 8%; P=0.03) in the CD5-positive group. A tendency to a more mutated IGHV status in the CD5 positive cases was observed (80% versus 54.5%; (P=0.11). No significant differences in outcome were found in relation to CD5 expression.
This study confirms the existence of cases of CD5-positive splenic marginal zone B-cell lymphoma and shows that these cases are closely related to classical splenic marginal zone lymphoma. Whether or not CD5-positive splenic marginal zone B-cell lymphoma constitutes a true subset obviously requires the study of more cases.
经典的脾边缘区 B 细胞淋巴瘤的特征是缺乏 CD5 表达。已经描述了在血液研究中诊断为表现出 CD5 表达的明显脾边缘区 B 细胞淋巴瘤的病例;然而,在没有组织学证据的情况下,由于可能与其他 CD5 阳性小 B 细胞肿瘤混淆,这些病例的正确诊断存在争议。
我们报告了一系列 24 例 CD5 阳性、t(11;14)-阴性的脾边缘区 B 细胞淋巴瘤病例,这些病例通过血液的流式细胞术研究和脾切片的组织学证实。评估了临床数据以及形态学、免疫学、细胞遗传学和分子特征,以评估这些病例与经典 CD5 阴性脾边缘区 B 细胞淋巴瘤的异同。
流式细胞术在血液中检测到的 CD5 表达在大多数情况下通过脾切片的免疫组化得到证实。一般来说,CD5 阳性和 CD5 阴性的脾边缘区 B 细胞淋巴瘤病例似乎没有不同,特别是它们表现出相似的细胞遗传学改变,如 7q 缺失、三体 3、三体 18 和偏倚的 IGHV 利用(即 VH1-2)。主要区别在于 CD5 阳性组的诊断时淋巴细胞计数更高(8.15x10(9)/L 与 3.90x10(9)/L;P=0.005)和更频繁的弥漫性骨髓浸润(34%与 8%;P=0.03)。在 CD5 阳性病例中观察到 IGHV 状态更倾向于突变的趋势(80%与 54.5%;P=0.11)。未发现 CD5 表达与预后有显著差异。
本研究证实了 CD5 阳性脾边缘区 B 细胞淋巴瘤的存在,并表明这些病例与经典的脾边缘区淋巴瘤密切相关。CD5 阳性脾边缘区 B 细胞淋巴瘤是否构成真正的亚群显然需要更多病例的研究。