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结节性淋巴细胞为主型霍奇金淋巴瘤患者的骨髓累及。

Bone Marrow Involvement in Patients With Nodular Lymphocyte Predominant Hodgkin Lymphoma.

机构信息

Departments of Hematopathology.

Lymphoma/Myeloma.

出版信息

Am J Surg Pathol. 2018 Apr;42(4):492-499. doi: 10.1097/PAS.0000000000001005.

Abstract

The spectrum of bone marrow lesions in patients with nodular lymphocyte predominant Hodgkin lymphoma (NLPHL) has not been evaluated systematically. In this study, we analyzed a cohort of 262 NLPHL patients who underwent staging bone marrow evaluation or targeted bone biopsy as a part of their initial diagnostic workup, among which lymphoma was detected in 24 (9.2%) patients. Eleven patients had bone marrow findings of NLPHL (few large B cells in a background of small B cell and T cell), and 13 patients had either T-cell/histiocyte-rich large B-cell lymphoma (large B cells in a background of T cells and histiocytes) or typical diffuse large B-cell lymphoma (sheets of large B cells). Bone marrow involvement was more common in patients with variant NLPHL histologic patterns in the lymph node as compared with those who had classic patterns (12/18 vs. 4/16; P=0.02). An additional 27 NLPHL patients had bone marrow specimens involved by lymphoid aggregates composed of small T cells and B cells without large B cells; this subgroup had a longer event-free survival than patients with lymphoma in the bone marrow (145 vs. 35 mo). Disease recurrence or progression was more frequent in patients with bone marrow involvement by either NLPHL or LBCL, compared with patients who had lymphoid aggregates (13/21 vs. 8/26; P=0.04). In conclusion, staging bone marrow sampling detects lymphoma in a sizeable subset of NLPHL patients, particularly those with variant histologic patterns. Lymphoid aggregates lacking large B cells in staging bone marrow specimens from NLPHL patients can be regarded as clinically benign without impact on stage, outcome, or risk stratification.

摘要

结节性淋巴细胞为主型霍奇金淋巴瘤(NLPHL)患者的骨髓病变谱尚未得到系统评估。在这项研究中,我们分析了 262 例 NLPHL 患者的队列,这些患者在初始诊断评估中进行了分期骨髓评估或靶向骨髓活检,其中 24 例(9.2%)患者中发现了淋巴瘤。11 例患者的骨髓发现为 NLPHL(小 B 细胞背景中有少量大 B 细胞),13 例患者为 T 细胞/组织细胞丰富的大 B 细胞淋巴瘤(T 细胞和组织细胞背景中有大 B 细胞)或典型弥漫性大 B 细胞淋巴瘤(大 B 细胞成片)。与经典形态相比,淋巴结中具有变异 NLPHL 组织学形态的患者骨髓受累更为常见(12/18 例比 4/16 例;P=0.02)。另外 27 例 NLPHL 患者的骨髓标本中有由小 T 细胞和 B 细胞组成的淋巴样聚集物,但无大 B 细胞;该亚组的无事件生存时间长于骨髓中存在淋巴瘤的患者(145 比 35 个月)。与有淋巴样聚集物的患者相比,骨髓受累的 NLPHL 或 LBCL 患者疾病复发或进展更为频繁(13/21 例比 8/26 例;P=0.04)。总之,分期骨髓采样可在相当一部分 NLPHL 患者中检测到淋巴瘤,特别是那些具有变异组织学形态的患者。NLPHL 患者分期骨髓标本中缺乏大 B 细胞的淋巴样聚集物可被视为临床良性,对分期、预后或风险分层无影响。

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