Tabata Rie, Iwama Hideaki, Tabata Chiharu, Yasumizu Ryoji, Kojima Masaru
Departments of Hematology and Oncology, Hyogo Prefectural Tsukaguchi Hospital.
J Clin Exp Hematop. 2014;54(2):155-61. doi: 10.3960/jslrt.54.155.
We report a rare primary splenic diffuse large B-cell lymphoma demonstrating CD5(+) and CD23(+) with very low CD20 expression. The only lesion was detected in the spleen, which was extremely enlarged with multiple large white-colored nodules. The lesion was characterized by a diffuse growth pattern of medium- to large-sized lymphoma cells with abundant cytoplasm. Immunohistochemical and flow cytometric study demonstrated that the lymphoma cells were negative for CD2, CD3, CD4, CD8, CD10, CD56, CD138, ALK-1, λ-light chain, and cyclin-D1, and positive for CD5, CD19, CD23, CD25, CD38, CD43, CD79a, IgM, IgD, κ-light chain, BCL2, BCL6, BOB. 1, Oct-2, Pax5, and MUM-1. CD20 was very weakly positive immunohistochemically, and negative by flow cytometric analysis. These findings resembled Richter syndrome, although chronic lymphocytic leukemia was not preexisting. Extremely poor outcome might be supposed because the effect of rituximab might be quite limited since CD20 was very weakly positive, in addition to an inferior prognosis of both CD20(-) and CD5(+) diffuse large B-cell lymphoma. Careful management is thus necessary.
我们报告了一例罕见的原发性脾脏弥漫性大B细胞淋巴瘤,其表现为CD5(+)、CD23(+),CD20表达极低。唯一的病灶位于脾脏,脾脏极度肿大,有多个白色大结节。该病灶的特征是中等至大尺寸淋巴瘤细胞呈弥漫性生长模式,细胞质丰富。免疫组织化学和流式细胞术研究表明,淋巴瘤细胞CD2、CD3、CD4、CD8、CD10、CD56、CD138、ALK-1、λ轻链和细胞周期蛋白D1呈阴性,而CD5、CD19、CD23、CD25、CD38、CD43、CD79a、IgM、IgD、κ轻链、BCL2、BCL6、BOB.1、Oct-2、Pax5和MUM-1呈阳性。CD20免疫组织化学染色呈极弱阳性,流式细胞术分析呈阴性。这些发现类似于里氏综合征,尽管之前不存在慢性淋巴细胞白血病。由于CD20呈极弱阳性,利妥昔单抗的效果可能非常有限,此外CD20(-)和CD5(+)弥漫性大B细胞淋巴瘤的预后较差,因此可能预后极差。因此需要谨慎处理。