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本文引用的文献

1
Low-Dose Methotrexate Toxicity Presenting as Pancytopenia.低剂量甲氨蝶呤毒性表现为全血细胞减少。
Cureus. 2022 Dec 13;14(12):e32494. doi: 10.7759/cureus.32494. eCollection 2022 Dec.
2
High prevalence of rheumatoid arthritis and its risk factors among Tibetan highlanders living in Tsarang, Mustang district of Nepal.尼泊尔马纳斯鲁地区塔桑地区的藏人高海拔居民中类风湿关节炎及其危险因素的高发率。
J Physiol Anthropol. 2022 Apr 2;41(1):12. doi: 10.1186/s40101-022-00283-3.
3
Hypoplastic myelodysplastic syndrome and acquired aplastic anemia: Immune‑mediated bone marrow failure syndromes (Review).发育不全性骨髓增生异常综合征和获得性再生障碍性贫血:免疫介导的骨髓衰竭综合征(综述)。
Int J Oncol. 2022 Jan;60(1). doi: 10.3892/ijo.2021.5297. Epub 2021 Dec 27.
4
Management of Rheumatoid Arthritis: An Overview.类风湿关节炎的治疗:概述。
Cells. 2021 Oct 23;10(11):2857. doi: 10.3390/cells10112857.
5
Potential contributors to low dose methotrexate toxicity in a patient with rheumatoid arthritis and pernicious anemia: case report.类风湿关节炎合并恶性贫血患者低剂量甲氨蝶呤毒性的潜在影响因素:病例报告
BMC Rheumatol. 2021 Feb 12;5(1):5. doi: 10.1186/s41927-020-00175-y.
6
Methotrexate Discontinuation and Dose Decreases After Therapy With Tocilizumab: Results From the Corrona Rheumatoid Arthritis Registry.托珠单抗治疗后甲氨蝶呤的停用及剂量减少:来自Corrona类风湿关节炎注册研究的结果
Rheumatol Ther. 2020 Jun;7(2):357-369. doi: 10.1007/s40744-020-00200-z. Epub 2020 Mar 30.
7
Methotrexate-induced myelodysplasia mimicking myelodysplastic syndrome.甲氨蝶呤诱导的骨髓发育异常综合征,酷似骨髓增生异常综合征。
Blood Res. 2018 Dec;53(4):268. doi: 10.5045/br.2018.53.4.268. Epub 2018 Dec 17.
8
Rheumatoid Arthritis: A Brief Overview of the Treatment.类风湿关节炎:治疗简述。
Med Princ Pract. 2018;27(6):501-507. doi: 10.1159/000493390. Epub 2018 Sep 2.
9
Clinical characteristics and risk factors for low dose methotrexate toxicity: a cohort of 28 patients.低剂量甲氨蝶呤毒性的临床特征和危险因素:一项 28 例患者的队列研究。
Autoimmun Rev. 2014 Nov;13(11):1109-13. doi: 10.1016/j.autrev.2014.08.027. Epub 2014 Aug 27.
10
Long-term safety of methotrexate monotherapy in patients with rheumatoid arthritis: a systematic literature research.甲氨蝶呤单药治疗类风湿关节炎患者的长期安全性:一项系统文献研究
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发育不全性骨髓增生异常综合征:类风湿关节炎中甲氨蝶呤毒性的症状

Hypoplastic Myelodysplastic Syndrome: Symptom of Methotrexate Toxicity in Rheumatoid Arthritis.

作者信息

Khan Adil, Anwar Maryem, Azam Adila, Nisar Sarah, Rehman Anees Ur

机构信息

Internal Medicine, Khyber Medical College, Peshawar, PAK.

Family Medicine, NHS (National Health Service), Slough, GBR.

出版信息

Cureus. 2023 Jun 17;15(6):e40580. doi: 10.7759/cureus.40580. eCollection 2023 Jun.

DOI:10.7759/cureus.40580
PMID:37469807
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10352143/
Abstract

Methotrexate is the conventional disease-modifying anti-rheumatic drug (DMARD) which is considered the drug of choice in the treatment of rheumatoid arthritis, but its prolonged use without monitoring leads to a number of complications involving different body systems. The toxic effects of long-term methotrexate (MTX) therapy mainly involve the liver, skin, gastrointestinal tract (GIT) and bone marrow. In the bone marrow, it mainly causes suppression of normal functionality, leading to the formation of abnormal blast cells and dysplasia. In this case report, we present a male patient with symptoms of hoarseness, fatigue and abnormal bleeding all of which can be affiliated with methotrexate-induced hypoplastic myelodysplasia. As pancytopenia can be a lethal complication of MTX toxicity, it is important to monitor the therapy and dosage of methotrexate so that in case of any unforeseen development of a complication vital steps may be taken to diagnose and treat it in time. Regarding our patient, after thorough history taking and undergoing extensive hematological workup, the diagnosis of MTX-induced hypoplastic myelodysplasia was made. His symptoms improved on withholding the drug methotrexate from his active regimen and adding folinic acid and colony-stimulating factors.

摘要

甲氨蝶呤是传统的改善病情抗风湿药(DMARD),被认为是治疗类风湿关节炎的首选药物,但其长期使用且无监测会导致涉及不同身体系统的多种并发症。长期甲氨蝶呤(MTX)治疗的毒性作用主要累及肝脏、皮肤、胃肠道(GIT)和骨髓。在骨髓中,它主要导致正常功能受到抑制,进而形成异常原始细胞和发育异常。在本病例报告中,我们介绍了一名男性患者,其出现声音嘶哑、疲劳和异常出血等症状,所有这些都可能与甲氨蝶呤诱导的发育不全性骨髓发育异常有关。由于全血细胞减少可能是MTX毒性的致命并发症,因此监测甲氨蝶呤的治疗和剂量很重要,以便在出现任何不可预见的并发症发展时能够及时采取关键步骤进行诊断和治疗。对于我们的患者,在进行全面的病史采集并接受广泛的血液学检查后,做出了MTX诱导的发育不全性骨髓发育异常的诊断。停用甲氨蝶呤并添加亚叶酸和集落刺激因子后,他的症状有所改善。