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低风险儿童结节性淋巴细胞为主型霍奇金淋巴瘤的组织学变异、IgD和CD30表达:儿童肿瘤学组报告

Variant histology, IgD and CD30 expression in low-risk pediatric nodular lymphocyte predominant Hodgkin lymphoma: A report from the Children's Oncology Group.

作者信息

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

机构信息

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.

出版信息

Pediatr Blood Cancer. 2018 Jan;65(1). doi: 10.1002/pbc.26753. Epub 2017 Aug 12.

Abstract

BACKGROUND

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.

PROCEDURE

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

程序

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%。

结果

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d4c/5699946/2d909d9e6439/nihms915720f1.jpg

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