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托珠单抗治疗类风湿关节炎合并骨髓增生异常综合征的有效性:一例病例报告及文献综述

Usefulness of tocilizumab for treating rheumatoid arthritis with myelodysplastic syndrome: A case report and literature review.

作者信息

Sun Chuanyin, Luo Yingwan, Tong Hongyan, Xu Guanhua, Lin Jin

机构信息

Department of Rheumatology Department of Hematology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.

出版信息

Medicine (Baltimore). 2018 Jun;97(25):e11179. doi: 10.1097/MD.0000000000011179.

Abstract

RATIONALE

Dysregulated immune function in rheumatoid arthritis (RA) might lead to the development of myelodysplastic syndrome (MDS). Serum interleukin-6 (IL-6) concentrations are increased in both RA and MDS patients.

PATIENT CONCERNS

A 58-year-old woman presented with severe RA. During a recent 8-month period, the patient experienced swelling in multiple joints, dizziness, and severe anemia. The symptoms responded poorly to oral corticosteroids and methotrexate (MTX). Even treatment of the patient's anemia by transfusion of red blood cells was ineffective. Laboratory tests showed high levels of IL-6 (214.24 pg/mL).

DIAGNOSES

Combining her medical history with clinical and laboratory parameters, especially those obtained by bone marrow aspiration, a diagnosis of RA with MDS was made.

INTERVENTIONS

MTX was discontinued and the patient was given tocilizumab intravenously at a dose of 8 mg/kg every 4 weeks and oral corticosteroids (15 mg/QD).

OUTCOMES

The patient's serological, physical, and pathological abnormalities improved significantly.

LESSONS

We report a case of RA with MDS successfully treated with tocilizumab. To our knowledge, this is the first case of an RA patient with MDS that was successfully treated with tocilizumab. In addition, our case emphasizes that IL-6 plays a critical role in the pathogenesis of RA with MDS. Tocilizumab might be an effective treatment for RA with MDS, especially in those with high levels of IL-6, elevated C-reactive protein, and severe anemia.

摘要

理论依据

类风湿关节炎(RA)中免疫功能失调可能导致骨髓增生异常综合征(MDS)的发生。RA和MDS患者的血清白细胞介素-6(IL-6)浓度均升高。

患者情况

一名58岁女性,患有严重RA。在最近8个月期间,该患者出现多关节肿胀、头晕和严重贫血。口服皮质类固醇和甲氨蝶呤(MTX)对症状的缓解效果不佳。即使通过输注红细胞治疗患者的贫血也无效。实验室检查显示IL-6水平很高(214.24 pg/mL)。

诊断

结合患者病史以及临床和实验室参数,尤其是通过骨髓穿刺获得的参数,诊断为RA合并MDS。

干预措施

停用MTX,给予患者托珠单抗静脉注射,剂量为每4周8 mg/kg,并口服皮质类固醇(15 mg/每日一次)。

结果

患者的血清学、身体和病理学异常得到显著改善。

经验教训

我们报告了一例用托珠单抗成功治疗的RA合并MDS病例。据我们所知,这是首例用托珠单抗成功治疗的RA合并MDS患者。此外,我们的病例强调IL-6在RA合并MDS的发病机制中起关键作用。托珠单抗可能是治疗RA合并MDS的有效药物,尤其是对于那些IL-6水平高、C反应蛋白升高和严重贫血的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0c9/6023877/803954a3d249/medi-97-e11179-g001.jpg

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