卡麦角林和小剂量类固醇治疗İn特发性肉芽肿性乳腺炎

Cemalettin DURGUN
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 Methods: In this study, the files of patients who were treated with cabergoline and steroids for idiopathic granulomatous mastitis in our clinic were reviewed retrospectively. 36 patients were included in the study. The patients were invited to the outpatient clinic for the final examination. Demographic characteristics of the patients, symptoms at presentation, examination findings, laboratory tests, radiological imaging, tru-cut biopsy results, microbiological culture results, treatment doses and durations, remission times, surgery requirements, and recurrence were recorded.
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引用次数: 0

摘要

特发性肉芽肿性乳腺炎(IGM)是一种罕见的乳腺慢性肉芽肿性炎症性疾病。它主要见于有母乳喂养史的年轻妇女。它通常表现为乳房疼痛的肿块、红斑、局灶性脓肿形成、皮肤溃疡或瘘管。IGM的病因和发病机制尚不清楚。它被认为是由于先前的高泌乳素血症引起的局部自身免疫反应,以对抗从小叶中泄漏的富含脂肪和蛋白质的分泌物。目前还没有明确的IGM治疗方案。药物治疗和手术治疗可单独或联合使用。在这项研究中,我们的目的是检查在我们中心接受卡麦角林和小剂量类固醇治疗IGM的患者的结果。方法:回顾性分析本院治疗特发性肉芽肿性乳腺炎同时应用卡麦角林和类固醇治疗的病例。36例患者纳入研究。患者被邀请到门诊进行期末检查。记录患者的人口学特征、首发症状、检查结果、实验室检查、放射成像、真切活检结果、微生物培养结果、治疗剂量和持续时间、缓解时间、手术要求和复发。 结果:本组36例患者均为育龄妇女。最常见的主诉是可触及的疼痛肿块。12例患者出现脓肿。9例出现溃疡,4例出现瘘管。最常见的受累部位是下外侧象限。1例患者培养中检出金黄色葡萄球菌。治疗后,36例患者中有20例完全康复。平均缓解时间为2.85±2.54个月。29例(74.3%)患者完成医学治疗。7例有残余肿块者行手术切除。随访27.88±8.21个月,无复发。结论:IGM的治疗仍存在争议。事实上,卡麦角林和低剂量类固醇治疗在短时间内缓解,减少了手术的需要,并且在中期随访中不会复发,这表明它是IGM治疗的成功选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cabergoline and Low-Dose Steroid Therapy İn Idiopathic Granulomatous Mastitis
Introduction: Idiopathic granulomatous mastitis(IGM) is a rare, chronic granulomatous inflammatory disease of the breast. It is mostly seen in young women with a history of breastfeeding. It typically presents as a painful lump in the breast, erythema, focal abscess formation, skin ulceration, or fistula. The etiology and pathogenesis of IGM could not yet be well understood. It is thought to be caused by a localized autoimmune response against fat and protein-rich secretions leaking from the lobules due to previous hyperprolactinemia. There is no definite treatment protocol defined for IGM. Pharmacological agents and surgical interventions are used alone or in combination in the treatment. In this study, we aimed to examine the results of patients who were treated with cabergoline and low-dose steroids for IGM in our center. Methods: In this study, the files of patients who were treated with cabergoline and steroids for idiopathic granulomatous mastitis in our clinic were reviewed retrospectively. 36 patients were included in the study. The patients were invited to the outpatient clinic for the final examination. Demographic characteristics of the patients, symptoms at presentation, examination findings, laboratory tests, radiological imaging, tru-cut biopsy results, microbiological culture results, treatment doses and durations, remission times, surgery requirements, and recurrence were recorded. Results: All 36 patients included in the study were women of childbearing age. The most common presenting complaint was a palpable painful mass. Abscesses were present in 12 patients. Ulcers were observed in 9 patients and fistulas were observed in 4 patients. The most common involvement was in the lower outer quadrant. S.aureus was detected in the culture of 1 patient. Complete recovery was observed in 20 of 36 patients as a result of the treatment. The mean duration of remission was 2.85±2.54 months. The treatment of 29 (74.3%) patients was completed medically. Surgical excision was performed in 7 patients with a residual lump. No recurrence was observed during the follow-up period of 27.88 ± 8.21 months. Conclusion: The treatment of IGM is still controversial. The fact that cabergoline and low-dose steroid therapy provides remission in a short time, minimizes the need for surgery, and does not relapse in medium-term follow-up shows that it is a successful option in IGM treatment.
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