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

IF 0.7 Q4 HEMATOLOGY
Case Reports in Hematology Pub Date : 2025-08-21 eCollection Date: 2025-01-01 DOI:10.1155/crh/9950134
Nehaal Ahmed, Saad Rashid, Nadeem Kutaish, Mohammed M Ahmed
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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.

Abstract Image

慢性tnf - α抑制的类风湿关节炎患者CD23阴性CLL/SLL的初始表现为皮下白血病。
类风湿性关节炎(RA)是一种慢性、全身性和自身免疫性疾病,以关节炎症和疼痛为特征。虽然RA和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CLL是罕见的。结外表现的CLL/SLL是罕见的。虽然皮肤受累是最常见的结外表现之一,但皮肤白血病是罕见的。此外,皮下皮肤白血病作为CLL/SLL的初始表现是非常罕见的。我们描述了一个慢性tnf - α抑制的长期RA患者,他表现出孤立的皮下肿块。切除活检显示小的、均匀的、成熟的淋巴细胞片,流式细胞术分析显示单克隆b细胞群CD23表达阴性,但CD5、CD19、CD20、CD38、kappa轻链和CD200表达阳性。进一步免疫染色cyclin-D1和SOX11为阴性,CD43和LEF1为阳性,总体上与CLL/ sll诱导的皮下白血病皮肤一致。虽然CLL/ sll诱导的皮肤白血病的治疗方法各不相同,但在本例中,巩固性局部放疗导致剩余皮肤病变的消退。当考虑在有淋巴瘤病史的患者中使用tnf - α抑制剂时,建议谨慎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
13 weeks
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