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复发性自身免疫性内耳疾病伴甲氨蝶呤和硫唑嘌呤联合治疗显著反应:病例报告及文献复习。

Relapsing autoimmune inner ear disease with significant response to methotrexate and azathioprine combination therapy: A case report and mini literature review.

机构信息

Department of Education, Shin Kong Wu Ho Su Memorial Hospital, Taipei, Taiwan.

Department of Education, Taichung Veterans General Hospital, Taichung, Taiwan.

出版信息

Medicine (Baltimore). 2023 Jun 9;102(23):e33889. doi: 10.1097/MD.0000000000033889.

Abstract

RATIONALE

Autoimmune inner ear disease typically presents with bilateral hearing loss that progresses over weeks or months though its mechanisms are unknown. Corticosteroids are the first-line treatment, but their responses are variable and relapses are frequent. Thus, many experts have sought to replace corticosteroids with immunosuppressive agents.

PATIENT CONCERNS

A 35-year-old woman experienced a progressive hearing impairment, initially on the left side and later becoming bilateral. Her response to corticosteroid monotherapy was temporary, and there have been two relapse episodes over several months.

DIAGNOSES

Autoimmune inner ear disease was considered due to evidence of autoimmunity combined with a clinical course of bilateral and recurrent sensorineural hearing loss and a partial response to corticosteroid therapy.

INTERVENTIONS

The patient received a 3-day mini-pulse of methylprednisolone at 250 mg/d, followed by 12 mg/d maintenance, and concurrently began an azathioprine regimen gradually increasing to 100 mg/day as a corticosteroid-sparing agent.

OUTCOMES

Three weeks after immunosuppressive therapy, hearing and pure-tone audiometry improved, and after 7 weeks, methylprednisolone was tapered to 8 mg/d. The dosage was further reduced by adding methotrexate at 7.5 mg/week, resulting in a reduction to 4 mg/d as maintenance therapy after 4 weeks.

LESSONS

For patients who are unresponsive to corticosteroids or experience difficulty tolerating them, a combination therapy of methotrexate and azathioprine is recommended as a viable alternative as this regimen is well-tolerated and yields positive outcomes.

摘要

背景

自身免疫性内耳病通常表现为双侧听力损失,其进展过程为数周或数月,但发病机制尚不清楚。皮质类固醇是一线治疗药物,但它们的疗效各异,且容易复发。因此,许多专家试图用免疫抑制剂替代皮质类固醇。

患者情况

一名 35 岁女性出现进行性听力下降,最初为左侧,后来双侧均出现。她对皮质类固醇单一疗法的反应是暂时的,并且在几个月内出现了两次复发。

诊断

考虑到自身免疫的证据以及双侧和复发性感觉神经性听力损失的临床过程,以及对皮质类固醇治疗的部分反应,诊断为自身免疫性内耳病。

干预措施

患者接受了为期 3 天的 250mg/d 甲泼尼龙小剂量冲击治疗,随后每天维持 12mg 治疗,同时开始逐渐增加至 100mg/天的硫唑嘌呤方案作为皮质类固醇节省剂。

结果

免疫抑制治疗 3 周后,听力和纯音听阈改善,7 周后,甲泼尼龙逐渐减少至 8mg/d。通过每周添加 7.5mg 甲氨蝶呤进一步减少剂量,4 周后将剂量减少至 4mg/d 作为维持治疗。

经验教训

对于对皮质类固醇无反应或难以耐受的患者,推荐使用甲氨蝶呤和硫唑嘌呤联合治疗作为一种可行的替代方案,因为该方案耐受性良好,且疗效良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cae4/10256420/07093bdadc79/medi-102-e33889-g001.jpg

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