Suppr超能文献

肉芽肿性多血管炎:复发性乳腺脓肿的罕见病因。

Granulomatosis With Polyangiitis: A Rare Cause of Recurrent Breast Abscesses.

作者信息

Bothara Rishi, Umer Imran, Bhalodia Alisha, Rehman Muneeb, Amar Zain

机构信息

Internal Medicine, University of Illinois, Peoria, USA.

Rheumatology, University of Illinois, Peoria, USA.

出版信息

Cureus. 2024 Jul 20;16(7):e64993. doi: 10.7759/cureus.64993. eCollection 2024 Jul.

Abstract

This case report highlights the importance of recognizing granulomatosis with polyangiitis (GPA) as a rare but potential cause of recurrent granulomatous mastitis and breast abscesses. The case report describes a patient who presented with recurrent breast abscesses over many years, initially misdiagnosed as infectious mastitis, until a breast tissue biopsy revealed granulomatous inflammation. Further evaluation confirmed the diagnosis of GPA based on elevated anti-neutrophil cytoplasmic antibodies (ANCA). The authors emphasize that, while breast involvement is exceedingly rare in GPA, it should be considered in cases of refractory granulomatous mastitis, even in the absence of typical systemic GPA manifestations. Early recognition can prevent misdiagnosis, allow timely initiation of immunosuppressive treatment, and avoid unnecessary procedures. The report calls for improved awareness and further research into the clinical characteristics and optimal management strategies for GPA presenting with breast lesions.

摘要

本病例报告强调了认识肉芽肿性多血管炎(GPA)作为复发性肉芽肿性乳腺炎和乳腺脓肿的一种罕见但潜在病因的重要性。该病例报告描述了一名多年来反复出现乳腺脓肿的患者,最初被误诊为感染性乳腺炎,直到乳腺组织活检显示肉芽肿性炎症。进一步评估基于抗中性粒细胞胞浆抗体(ANCA)升高确诊为GPA。作者强调,虽然GPA累及乳腺极为罕见,但在难治性肉芽肿性乳腺炎病例中应予以考虑,即使没有典型的全身性GPA表现。早期识别可防止误诊,允许及时开始免疫抑制治疗,并避免不必要的手术。该报告呼吁提高对伴有乳腺病变的GPA的认识,并进一步研究其临床特征和最佳管理策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0260/11332569/85a6b8d5874d/cureus-0016-00000064993-i01.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验