Successful treatment of anti-signal recognition particle antibody-positive myositis with intravenous cyclophosphamide: A case report.

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
Fukushima Journal of Medical Science Pub Date : 2025-01-18 Epub Date: 2024-12-07 DOI:10.5387/fms.24-00013
Jumpei Temmoku, Shuhei Yoshida, Kanae Tsuchihashi, Yuya Sumichika, Kenji Saito, Haruki Matsumoto, Yuya Fujita, Naoki Matsuoka, Tomoyuki Asano, Nozomu Matsuda, Shuzo Sato, Kiyoshi Migita
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引用次数: 0

Abstract

Myositis-specific autoantibodies play an important role on the disease phenotype of idiopathic inflammatory myopathies (IIMs). Anti-signal recognition particle (SRP) antibody-positive patients with IIMs may present with severe myopathy and highly elevated serum creatine kinase levels. These patients are often resistant to immunosuppressive therapy, but there is no established treatment strategy. A 51-year-old man referred to our department was diagnosed with IIM based on imaging and pathological findings. A high dose of corticosteroids followed by intravenous cyclophosphamide (IV-CY) treatment (750 mg three times) resulted in an improvement in clinical manifestations and functional outcomes, and recurrence did not occur. Our case suggests that IV-CY is an effective induction regimen for patients with anti-SRP antibody-positive IIMs.

静脉注射环磷酰胺成功治疗抗信号识别颗粒抗体阳性肌炎1例。
肌炎特异性自身抗体在特发性炎症性肌病(IIMs)的疾病表型中起重要作用。抗信号识别颗粒(SRP)抗体阳性的IIMs患者可能表现为严重的肌病和血清肌酸激酶水平的高度升高。这些患者通常对免疫抑制治疗有耐药性,但目前还没有确定的治疗策略。一名51岁男性,经影像学及病理诊断为IIM。高剂量皮质类固醇后静脉注射环磷酰胺(IV-CY)治疗(750 mg,三次)可改善临床表现和功能结果,且未发生复发。我们的病例表明IV-CY是抗srp抗体阳性IIMs患者的有效诱导方案。
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来源期刊
Fukushima Journal of Medical Science
Fukushima Journal of Medical Science MEDICINE, GENERAL & INTERNAL-
CiteScore
1.70
自引率
12.50%
发文量
24
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