特发性肉芽肿性乳腺炎女性患者的风湿病表现

IF 1 Q4 RHEUMATOLOGY
Ahmad Elahi , Amir Eyvazi , Ali Faegh , Golbarg Mehrpoor
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引用次数: 0

摘要

背景特发性肉芽肿性乳腺炎(IGM)是一种不常见的炎症性乳腺疾病,通常表现为单侧乳房肿块,有时为双侧乳房肿块,导致疼痛、红斑和乳头溢液。工作目的 评估转诊至伊玛目阿里医院(伊朗卡拉杰)的 IGM 女性患者的特征表现(包括风湿病)的频率。患者和方法 本研究的对象是转诊至伊玛目阿里医院乳腺外科的 178 名女性患者,根据核心针活检和组织病理学检查确诊为 IGM。结果患者的平均年龄为(35.17 ± 5.88)岁,体重指数为(26.38 ± 2.45)。91%的患者为未婚先孕,只有 3 人使用口服避孕药。准妈妈的哺乳期为(28.91 ± 14.97)个月。2.25%的患者伴有轻微地中海贫血,支气管哮喘、糖尿病、银屑病和甲状腺功能减退症各占 2 例。7例(3.92%)患者曾接受过乳腺手术。25 名(14%)IGM 患者伴有关节痛(10.11%)、关节炎(2.25%)和结节性红斑(2.81%)等表现。只有一名患者患有周围神经炎,另一名患者患有视神经炎。158名患者(88.76%)没有明显的既往病史。结论结节性红斑和关节炎与 IGM 并存的情况并不少见。结节性红斑和关节炎与 IGM 并存的情况并不少见。视神经和周围神经病很少伴发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rheumatologic manifestations of female patients with idiopathic granulomatous mastitis

Background

Idiopathic granulomatous mastitis (IGM) is an infrequent inflammatory breast disease that typically presents with unilateral and sometimes bilateral breast masses, leading to pain, erythema, and nipple discharge. IGM may be accompanied by extramammary symptoms, including episcleritis and arthralgia suggesting and underlying autoimmune process.

Aim of the work

To evaluate the frequency of characteristics manifestations including rheumatologic in females with IGM referred to Imam Ali Hospital (Karaj, Iran).

Patients and methods

This study was performed on 178 females referred to the breast surgery department of Imam Ali Hospital and diagnosed with IGM based on core needle biopsy and histopathological examination. The various manifestations including rheumatic presented for those patients were recorded.

Results

The mean age of the patients was 35.17 ± 5.88 years and body mass index was 26.38 ± 2.45. 91 % of the patients were nulliparous and only 3 used oral contraceptive pills. The breast-feeding duration of parous patients was 28.91 ± 14.97 months. Associated minor thalassemia was present in 2.25 %, bronchial asthma, diabetes, psoriasis and hypothyroidism were present in 2 patients each. 7 (3.92 %) of cases had history of previous breast surgery. Twenty-five (14 %) patients with IGM had associated manifestations including arthralgia (10.11 %), arthritis (2.25 %) and erythema nodosum (2.81 %). Only one patient had peripheral and another optic neuritis. 158 (88.76 %) patients had no notable past medical history. IGM was bilateral in 21 (11.8 %) patients.

Conclusions

The coexistence of erythema nodosum and arthritis with IGM is not uncommon. They are mostly unilaterally present in nulliparous Iranian females. Optic and peripheral neuropathies are rarely associated.

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来源期刊
Egyptian Rheumatologist
Egyptian Rheumatologist RHEUMATOLOGY-
CiteScore
2.00
自引率
22.20%
发文量
77
审稿时长
39 weeks
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