Liu Zach, Dong Henry Y, Gorczyca Wojciech, Tsang Patricia, Cohen Patti, Stephenson Christine F, Berger Carol S, Wu C Daniel, Weisberger James
IMPATH, New York, NY 10019, USA.
Am J Clin Pathol. 2002 Aug;118(2):216-24. doi: 10.1309/TE56-A43X-29TT-5H8G.
Mantle cell lymphoma (MCL) typically expresses B-cell antigens and CD5 and overexpresses bcl-1 protein. However, unusual cases of bcl-1+ and CD5-MCL have been observed, posing a practical challenge for correct diagnosis and management. We identified 25 cases (48 samples) of bcl-1+ and CD5- lymphoma. CD5 expression was assessed by flow cytometric analysis alone (1 case), immunohistochemical analysis alone (17 cases), or dual flow cytometric/immunohistochemical methods (7 cases). The morphologic features were consistent with MCL with centrocytic cytomorphology in 20 cases and blastic variant in 5 cases. The t(11;14) was confirmed in 8 of 11 cases by fluorescence in situ hybridization of paraffin-embedded tissue. Cytogenetic analysis revealed the t(11;14) within a complex karyotype in 2 additional cases. These data show that MCL may lack CD5 expression. Evaluation of bcl-1 expression by immunohistochemical analysis or molecular genetics may be indicated if MCL is suspected clinically or morphologically despite a lack of CD5 expression.
套细胞淋巴瘤(MCL)通常表达B细胞抗原和CD5,并过度表达bcl-1蛋白。然而,已经观察到bcl-1阳性和CD5阴性的MCL罕见病例,这对正确诊断和管理构成了实际挑战。我们鉴定了25例(48份样本)bcl-1阳性和CD5阴性淋巴瘤。CD5表达仅通过流式细胞术分析评估(1例)、仅通过免疫组织化学分析评估(17例)或通过流式细胞术/免疫组织化学双重方法评估(7例)。形态学特征在20例中与具有中心细胞形态的MCL一致,在5例中与母细胞变异型一致。通过石蜡包埋组织的荧光原位杂交在11例中的8例中证实了t(11;14)。细胞遗传学分析在另外2例复杂核型中发现了t(11;14)。这些数据表明MCL可能缺乏CD5表达。如果临床或形态学上怀疑为MCL,尽管缺乏CD5表达,仍可能需要通过免疫组织化学分析或分子遗传学评估bcl-1表达。