特发性肉芽肿性乳腺炎、结节性红斑和多关节炎。

IF 1.9 Q2 ORTHOPEDICS
Ali Tarhini, Georges El Hasbani, Lama Farhat, Diamond Ghieh, Imad Uthman
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引用次数: 0

摘要

特发性肉芽肿性乳腺炎(IGM)是一种炎症介导的罕见疾病,可能与罕见的表现有关。结节性红斑(EN)和多关节炎见于多种自身炎症和自身免疫性疾病,但很少与特发性肉芽肿性乳腺炎联系在一起。尽管 IGM 的病因尚不清楚,但人们认为科里纳杆菌感染在 IGM 的病理生理学中起了一定作用。不同寻常的是,IGM 具有复发和缓解的病程,这也适用于其全身表现。因此,我们介绍了一例 IGM 病例,患者是一名中年女性,起初被认为患有含棒状杆菌的单侧脓肿,并进行了引流。然而,几个没有细菌生长的脓肿开始复发,病程因EN和多关节炎而变得复杂。IGM、EN和多关节炎最终得到缓解,并通过对症治疗得到控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Idiopathic Granulomatous Mastitis, Erythema Nodosum, and Polyarthritis.

Idiopathic granulomatous mastitis (IGM) is an inflammatory-mediated rare disease that can be linked to rare manifestations. Erythema nodosum (EN) and polyarthritis, seen in a multitude of autoinflammatory and autoimmune diseases, have been rarely linked to IGM. Despite the cause of IGM being unclear, Corynebacterium infections are thought to play a role in the pathophysiology of IGM. Unusually, IGM has a relapsing and remitting course, which also applies to its systemic manifestations. As such, we present a case of IGM in a middle-aged lady who was initially thought to have Corynebacterium-containing unilateral abscesses for which drainage was performed. However, several abscesses devoid of bacterial growth started recurring, and the disease course was complicated by EN and polyarthritis. IGM, EN, and polyarthritis eventually resolved and were managed with symptomatic treatment.

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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
14
审稿时长
8 weeks
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