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伴有干燥综合征的慢性淋巴细胞白血病/小淋巴细胞淋巴瘤患者的 II 型冷球蛋白血症。

Type II cryoglobulinemia in a patient with chronic lymphocytic leukemia/small lymphocytic lymphoma and Sjögren's disease.

机构信息

Department of Hematology, the First Hospital of China Medical University, Shenyang, Liaoning, P. R. China.

出版信息

J Int Med Res. 2024 Nov;52(11):3000605241285228. doi: 10.1177/03000605241285228.

Abstract

Type II cryoglobulinemia is a rare disorder characterized by abnormal immunoglobulins (Igs) precipitating in the blood at low temperatures and redissolving upon warming. Sjogren's disease (SjD) is an autoimmune disorder involving secretory gland malfunction that leads to persistent dryness of the mouth and eyes. Here, we report the case of a 61-year-old woman with a 7-year history of SjD who was diagnosed with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). However, her complicated clinical features could not be sufficiently explained by this disease alone. Immunofixation electrophoresis revealed monoclonal IgM-κ and polyclonal IgG-κ. The presence of precipitated cryoglobulin and elevated rheumatoid factor levels confirmed a diagnosis of type II cryoglobulinemia for this patient. To the best of our knowledge, this case represents the first report of a patient with CLL/SLL, SjD, and type II cryoglobulinemia, which increased our understanding of immune system-related disorders. Because certain similar mechanisms are involved in the pathogenesis of these three diseases, a combination treatment of rituximab, ibrutinib, and dexamethasone resulted in a favorable prognosis for this patient.

摘要

Ⅱ型冷球蛋白血症是一种罕见的疾病,其特征是异常免疫球蛋白(Ig)在低温下沉淀在血液中,在升温后重新溶解。干燥综合征(SjD)是一种自身免疫性疾病,涉及分泌腺功能障碍,导致口腔和眼睛持续干燥。在这里,我们报告了一例 61 岁女性,患有 SjD7 年,被诊断为慢性淋巴细胞白血病/小淋巴细胞淋巴瘤(CLL/SLL)。然而,仅靠这种疾病并不能充分解释她复杂的临床特征。免疫固定电泳显示单克隆 IgM-κ 和多克隆 IgG-κ。沉淀冷球蛋白和类风湿因子水平升高的存在确诊了该患者的Ⅱ型冷球蛋白血症。据我们所知,这是首例 CLL/SLL、SjD 和Ⅱ型冷球蛋白血症患者的报告,增加了我们对免疫系统相关疾病的认识。由于这三种疾病的发病机制存在某些相似机制,因此利妥昔单抗、伊布替尼和地塞米松联合治疗为该患者带来了良好的预后。

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