Matsuda Ikuo, Shimizu Yoshifumi, Okamoto Takahiro, Hirota Seiichi
Department of Surgical Pathology, Hyogo College of Medicine Hyogo, Japan.
Department of Hematology, Takarazuka Municipal Hospital Hyogo, Japan.
Int J Clin Exp Pathol. 2014 Sep 15;7(10):7076-81. eCollection 2014.
Nodal follicular lymphoma (FL) is typically composed of follicular or nodular proliferation of small cleaved lymphoid cells, presumably derived from germinal center (GC) B cells. The hallmark of FL is t(14;18)(q32;q21) chromosomal translocation, which juxtaposes anti-apoptotic gene BCL2 to immunoglobulin heavy chain (IGH) promoter. Reflecting this background, FL cells are immunohistochemically positive for BCL2 as well as GC B cell markers CD10 and BCL6. It is known that low grade B-cell lymphomas, including FL, chronic lymphocytic leukemia/small lymphocytic lymphoma, and marginal zone lymphoma, are sometimes associated with marginal zone differentiation or plasmacytic differentiation. The marginal zone differentiation obscures the morphological differences among these, providing diagnostic challenges for histopathologists. In this paper, we present a case of FL, originally mimicking marginal zone lymphoma in the axillary lymph node. Subsequent bone marrow biopsy showed paratrabecular infiltration of small to medium-sized lymphoid cells. Immunohistochemical analysis of the bone marrow biopsy together with histopathology and flow cytometry of the axillary lymph node led to a final diagnosis of FL with marginal zone differentiation in the axillary lymph node and its bone marrow infiltration. Our case illustrates and reconfirms the importance of clinicopathological correlation which leads to a correct diagnosis.
结节性滤泡性淋巴瘤(FL)通常由小核裂淋巴样细胞的滤泡或结节状增生组成,推测其起源于生发中心(GC)B细胞。FL的特征是t(14;18)(q32;q21)染色体易位,该易位使抗凋亡基因BCL2与免疫球蛋白重链(IGH)启动子并列。反映这一背景,FL细胞免疫组化检测BCL2以及GC B细胞标志物CD10和BCL6呈阳性。已知包括FL、慢性淋巴细胞白血病/小淋巴细胞淋巴瘤和边缘区淋巴瘤在内的低级别B细胞淋巴瘤有时与边缘区分化或浆细胞分化相关。边缘区分化掩盖了这些疾病之间的形态学差异,给组织病理学家带来了诊断挑战。在本文中,我们报告了一例最初在腋窝淋巴结中类似边缘区淋巴瘤的FL病例。随后的骨髓活检显示小梁旁有小到中等大小的淋巴样细胞浸润。对骨髓活检进行免疫组化分析,并结合腋窝淋巴结的组织病理学和流式细胞术检查,最终诊断为腋窝淋巴结有边缘区分化且伴有骨髓浸润的FL。我们的病例说明了并再次证实了临床病理相关性对于正确诊断的重要性。