Untanu Ramona Vesna, Back Jason, Appel Burton, Pei Qinglin, Chen Lu, Buxton Allen, Hodgson David C, Ehrlich Peter F, Constine Louis S, Schwartz Cindy L, Hutchison Robert E
Division of Clinical Pathology, Department of Pathology, State University of New York Upstate Medical University, Syracuse, New York.
Department of Pathology, Chatham-Kent Health Alliance, Chatham, Ontario, Canada.
Pediatr Blood Cancer. 2018 Jan;65(1). doi: 10.1002/pbc.26753. Epub 2017 Aug 12.
Histologic prognostic factors have been described for nodular lymphocyte predominant Hodgkin lymphoma (NLPHL). This study examines histologic and immunophenotypic variants in a clinical trial for pediatric NLPHL.
One hundred sixty-eight cases of localized NLPHL were examined for histologic variants, CD30 and immunoglobulin D (IgD) expression, and outcome. Histologic types were scored categorically as 0 = 0, 1 ≤ 25%, and 2 > 25% of the sample.
Fifty-eight (35.1%) cases showed only typical nodular with or without serpiginous histology (types A and B). The remainder showed mixtures of histologies. The numbers of patients with score 2 are 85 (50.6%) type A, 21 (12.5%) type B, 46 (27.4%) with extranodular large B cells (type C), 3 with T-cell-rich nodular pattern (type D), 55 (32.7%) with diffuse T-cell-rich (type E) pattern, and 2 (1.2%) with diffuse B-cell pattern (type F). Higher level of types C (P = 0.048) and D (P = 0.033) resulted in lower event-free survival (EFS). Cytoplasmic IgD was found in 65 of 130 tested (50%), did not significantly associate with EFS but positively correlated with types C and E histology (P < 0.0001) and negatively correlated with types A (P = 0.0003) and B (P = 0.006). Seventeen (10%) expressed CD30, with no adverse effect.
Variant histology is common in pediatric NLPHL, especially types C and E, which are associated with IgD expression. Type C variant histology and possibly type D are associated with decreased EFS, but neither IgD nor CD30 are adverse features. Variant histology may warrant increased surveillance, but did not affect overall survival.
已描述了结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)的组织学预后因素。本研究在一项针对儿童NLPHL的临床试验中检测了组织学和免疫表型变异。
对168例局限性NLPHL病例进行了组织学变异、CD30和免疫球蛋白D(IgD)表达及预后检查。组织学类型按样本中所占比例分类评分:0 = 0,1≤25%,2>25%。
58例(35.1%)仅表现为典型结节性,伴或不伴匐行性组织学改变(A和B型)。其余病例表现为多种组织学改变混合。组织学评分2分的患者数量分别为:85例(50.6%)A型,21例(12.5%)B型,46例(27.4%)伴结节外大B细胞(C型),3例为富含T细胞的结节型(D型),55例(32.7%)为弥漫性富含T细胞型(E型),2例(1.2%)为弥漫性B细胞型(F型)。C型(P = 0.048)和D型(P = 0.033)比例较高导致无事件生存期(EFS)较低。在130例检测病例中有65例(50%)发现细胞质IgD,其与EFS无显著相关性,但与C型和E型组织学呈正相关(P < 0.0001),与A型(P = 0.0003)和B型(P = 0.006)呈负相关。17例(10%)表达CD30,无不良影响。
变异组织学在儿童NLPHL中常见,尤其是C型和E型,与IgD表达相关。C型变异组织学以及可能的D型与EFS降低有关,但IgD和CD30均不是不良特征。变异组织学可能需要加强监测,但不影响总生存期。