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免疫抑制治疗可使特发性肉芽肿性乳腺炎达到无药物缓解的目标。

Drug-free remission is an achievable target with immunosuppressive treatment in idiopathic granulomatous mastitis.

机构信息

Rheumatology Department, Gulhane Training and Research Hospital, University of Health Sciences Turkey, Ankara, Turkey.

出版信息

Ir J Med Sci. 2023 Dec;192(6):2815-2819. doi: 10.1007/s11845-023-03338-1. Epub 2023 Mar 16.

Abstract

BACKGROUND

Idiopathic granulomatous mastitis (IGM) is a rare inflammatory breast disease, in which there is no clear established treatment algorithm. Several physicians keep away from using immunosuppressive (IS) treatments in routine clinical practice.

AIMS

This study aimed to evaluate the rates of drug-free remission of the patients with IGM in a period of 3-year follow-up.

METHODS

This retrospective study conducted with 55 biopsy-proven IGM patients, who were followed up between February, 2011, and November, 2021, in rheumatology outpatient clinic of Gulhane Training and Research Hospital. The demographic and clinical characteristics of the patients were obtained from patients' files. The 3-year follow-up data were assessed for long-term outcome analyses.

RESULTS

There were 55 female patients with a mean age of 36.8 ± 6.3 years. Fifty-four (98.1%) patients were in drug-free remission at the end of 3 years. The median duration of drug-free remission in patients receiving methotrexate (MTX), only corticosteroid (CS), and azathioprine was 19.7, 32.9, and 14.7 months, respectively. The drug-free remission duration for the patient who received cyclosporine A as IS was 28.3 months. The median duration of IS treatment was 15.8 months, and the median duration of treatment with CS and other IS combination was 6.7 months. Recurrence was observed in 4 (80%) patients without IS therapy after surgery, of whom MTX was used in 3 (75%) patients and achieved remission.

CONCLUSIONS

IS agents provide high rate of prolonged drug-free remission and should be considered a part of routine medical care of the patients with IGM.

摘要

背景

特发性肉芽肿性乳腺炎(IGM)是一种罕见的炎症性乳腺疾病,目前尚无明确的治疗方案。一些医生在常规临床实践中避免使用免疫抑制剂(IS)治疗。

目的

本研究旨在评估 3 年随访期间 IGM 患者无药物缓解的比例。

方法

这项回顾性研究纳入了 55 例经活检证实的 IGM 患者,这些患者于 2011 年 2 月至 2021 年 11 月在古尔哈内培训与研究医院的风湿病门诊接受随访。从患者病历中获取患者的人口统计学和临床特征。对 3 年的随访数据进行评估,以进行长期结局分析。

结果

共有 55 名女性患者,平均年龄为 36.8±6.3 岁。54 例(98.1%)患者在 3 年后达到无药物缓解。接受甲氨蝶呤(MTX)、仅皮质类固醇(CS)和硫唑嘌呤治疗的患者无药物缓解的中位持续时间分别为 19.7、32.9 和 14.7 个月。接受环孢素 A 作为 IS 治疗的患者无药物缓解的中位持续时间为 28.3 个月。IS 治疗的中位持续时间为 15.8 个月,CS 和其他 IS 联合治疗的中位持续时间为 6.7 个月。4 例(80%)患者在手术后未接受 IS 治疗而复发,其中 3 例(75%)患者使用 MTX 并缓解。

结论

IS 药物可提供长期无药物缓解的高比例,应考虑将其作为 IGM 患者常规医疗护理的一部分。

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