d'Amore E S G, Menin A, Bonoldi E, Bevilacqua P, Cazzavillan S, Donofrio V, Gambini C, Forni M, Gentile A, Magro G, Boldrini R, Pillon M, Rosolen A, Alaggio R
Department of Pathology, Ospedale San Bortolo, Vicenza, Italy.
Pediatr Dev Pathol. 2007 May-Jun;10(3):181-91. doi: 10.2350/06-04-0082.1.
In this article, we describe the morphologic and immunophenotypic features of 75 cases of pediatric anaplastic large cell lymphoma (ALCL). According to the World Health Organization classification, 49 cases were common subtype ALCL, and respectively, 3, 6, and 17 cases were small cell, lymphohistiocytic, or mixed histologic variants. Anaplastic lymphoma kinase positivity was detected in 90.7% of the tumors and, using a panel of 9 T-cell surface markers, 88% could be assigned to the T-cell lineage. A molecular analysis for the T-cell receptor gamma (TCR- gamma) and the heavy chain of the immunoglobulin H rearrangements was performed on 6/9 ALCLs with a null immunophenotype, and a TCR clonal pattern was detected in 5/6 cases. In addition, 94.1% were immunoreactive for 1 or more cytotoxic proteins (Tia1, granzyme B, or perforin), and 15% expressed CD56. Clusterin, CD83, and Pax5, respectively, expressed in 91.3%, 1.7%, and 0% of the ALCLs, were useful biomarkers for the differential diagnosis with Hodgkin's lymphomas.
在本文中,我们描述了75例儿童间变性大细胞淋巴瘤(ALCL)的形态学和免疫表型特征。根据世界卫生组织分类,49例为常见亚型ALCL,小细胞、淋巴组织细胞或混合组织学变异型分别为3例、6例和17例。90.7%的肿瘤检测到间变性淋巴瘤激酶阳性,使用一组9种T细胞表面标志物,88%可归为T细胞系。对6/9例免疫表型阴性的ALCL进行了T细胞受体γ(TCR-γ)和免疫球蛋白H重链重排的分子分析,5/6例检测到TCR克隆模式。此外,94.1%对1种或更多细胞毒性蛋白(Tia1、颗粒酶B或穿孔素)呈免疫反应,15%表达CD56。Clusterin、CD83和Pax5分别在91.3%、1.7%和0%的ALCL中表达,是与霍奇金淋巴瘤鉴别诊断的有用生物标志物。