胚泡
套细胞淋巴瘤
免疫分型
CD5型
23号公路
病理
淋巴瘤
医学
抗原
免疫学
抗体
免疫球蛋白E
作者
Juehua Gao,LoAnn C. Peterson,Beverly P. Nelson,Charles L. Goolsby,Yihua Chen
标识
DOI:10.1309/ajcpv8ln5enmzovy
摘要
Abstract Mantle cell lymphoma (MCL) expresses pan–B-cell antigens and is usually CD5+/CD10−/CD23−/FMC7+. In this study, we evaluated 52 patients with confirmed diagnoses of MCL and identified variant immunophenotypes in 21 patients (19/48 classical and 2/4 variant MCLs), including CD5− in 6 (12%) of 52, CD10+ in 4 (8%) of 50, CD23+ in 10 (21%) of 48, and FMC7− in 4 (11%) of 37 cases. Three cases showed variations in 2 antigens, including CD5−/CD23+, CD10+/FMC7−, and CD23+/FMC7−; they were all classical MCLs. One blastoid variant MCL was CD23+, and one was FMC7−. Evaluation for proliferation index by immunohistochemical analysis for Ki-67 demonstrated no significant difference between MCLs with variant immunophenotypes and MCLs with typical immunophenotypes. The high proliferation index (>60%) was exclusively seen in the blastoid and pleomorphic variants. Our results indicate that immunophenotypic variations are common in MCL, and recognizing the variability is important for accurate subclassification of B-cell lymphoma.
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