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皮下白血病性皮肤浸润作为类风湿关节炎患者在慢性肿瘤坏死因子-α抑制治疗过程中CD23阴性慢性淋巴细胞白血病/小淋巴细胞淋巴瘤的初始表现

Subcutaneous Leukemia Cutis as the Initial Manifestation of CD23 Negative CLL/SLL in a Patient With Rheumatoid Arthritis on Chronic TNF-Alpha Inhibition.

作者信息

Ahmed Nehaal, Rashid Saad, Kutaish Nadeem, Ahmed Mohammed M

机构信息

Division of Internal Medicine, Mayo Clinic, Rochester, Minnesota, USA.

St. George's University School of Medicine, True Blue, Grenada.

出版信息

Case Rep Hematol. 2025 Aug 21;2025:9950134. doi: 10.1155/crh/9950134. eCollection 2025.

Abstract

Rheumatoid arthritis (RA) is a chronic, systemic, and autoimmune disease characterized by inflammation and pain in the joints. While RA and TNF-alpha inhibitors have historically been associated with an increased risk of lymphoma, chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) is infrequently seen. CD23 negative CLL is rare. Extranodal manifestations of CLL/SLL are uncommon. While cutaneous involvement is among the more common extranodal manifestations, leukemia cutis is rare. Furthermore, subcutaneous leukemia cutis as the initial manifestation CLL/SLL is exceedingly uncommon. We describe a patient with longstanding RA on chronic TNF-alpha inhibition who presented with an isolated subcutaneous mass. Excisional biopsy demonstrated sheets of small, uniform, and mature lymphocytes with flow cytometric analysis noting a monoclonal B-cell population negative for CD23 expression but positive for CD5, CD19, CD20, CD38, kappa light chain, and CD200 expression. Further immunostaining was negative for cyclin-D1 and SOX11 and positive for CD43 and LEF1, overall consistent with CLL/SLL-induced subcutaneous leukemia cutis. While treatments for CLL/SLL-induced leukemia cutis vary, in this case, consolidative local radiation led to resolution of the remaining cutaneous lesion. Caution is advised when considering the use of TNF-alpha inhibitors in patients with a history of lymphoma.

摘要

类风湿关节炎(RA)是一种慢性、全身性自身免疫性疾病,其特征为关节炎症和疼痛。虽然RA和肿瘤坏死因子-α(TNF-α)抑制剂历来与淋巴瘤风险增加相关,但慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(CLL/SLL)并不常见。CD23阴性的CLL很罕见。CLL/SLL的结外表现并不常见。虽然皮肤受累是较常见的结外表现之一,但皮肤白血病很少见。此外,以皮下白血病为CLL/SLL的初始表现极为罕见。我们描述了一名长期接受慢性TNF-α抑制治疗的RA患者,该患者出现了一个孤立的皮下肿块。切除活检显示有大量小的、形态一致且成熟的淋巴细胞,流式细胞术分析显示为单克隆B细胞群,CD23表达阴性,但CD5、CD19、CD20、CD38、κ轻链和CD200表达阳性。进一步免疫染色显示细胞周期蛋白D1和SOX11阴性,CD43和LEF1阳性,总体符合CLL/SLL诱导的皮下白血病。虽然CLL/SLL诱导的皮肤白血病的治疗方法各不相同,但在本病例中,巩固性局部放疗使剩余的皮肤病变得到缓解。对于有淋巴瘤病史的患者,在考虑使用TNF-α抑制剂时应谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7159/12393954/1fe4d73af68f/CRIHEM2025-9950134.001.jpg

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