特发性肉芽肿性乳腺炎的治疗:诊断和治疗的难题

N. Akhter, Abu Khaled Mohammad Lqbal, Md. Mahbubur Rahman, Joydeep Datta Gupta, A. Alam
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引用次数: 0

摘要

背景:特发性肉芽肿性乳腺炎是一种罕见的乳腺疾病。临床和放射学上可能与乳腺癌相似。迄今为止,IGM还没有公认的黄金标准治疗方法。临床治疗通常从消除微生物感染的测试开始,当微生物感染可以排除时,进行长期口服类固醇治疗或手术。目的:观察特发性肉芽肿性乳腺炎不同治疗方案的疗效。方法:本研究为回顾性研究,纳入2009年1月至2016年12月在我院治疗的50例IGM患者。结果:患者平均年龄34.3岁。乳房肿块是最常见的表现。右乳30例,左乳20例。4例患者就诊时已怀孕。4例患者在6个月内出现哺乳期。45名患者服用避孕药。17例临床怀疑为恶性肿瘤。20例患者行乳房x光检查,9例显示局灶性不对称致密病变,8例显示界限清楚的不透明,1例推测病变,2例正常。40例患者行细针抽吸。广泛的局部切除是主要的治疗方法。一名患者因复发而接受乳房切除术,最终组织学证实特发性肉芽肿性乳腺炎,无恶性肿瘤证据。12例患者平均随访31.2个月后出现复发。结论:IGM在我国并不罕见。临床、放射学、甚至细胞学表现有时与恶性肿瘤混淆。适当的手术治疗和辅助治疗是必要的。加强外科医生和病理学家之间的知识、意识和合作,避免不必要的误诊和治疗。外科杂志(2017)Vol. 21 (2): 89-93
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Management of idiopathic granulomatous mastitis: dilema in diagnosis and management
Background: Idiopathic granulomatous mastitis is a rare disease of the breast. Clinically and radiologically it may mimic breast carcinoma. To date, there is no agreed gold standard treatment for IGM. The clinical management often starts with tests to eliminate microbial infection and when microbial infection can be ruled out, long-term oral steroid treatment or surgery is administered. Objective: To see the response of different treatment options of idiopathic granulomatous mastitis. Methods: This is a retrospective study involved 50 patients who were diagnosed with IGM and were treated in our institution between January 2009 to December 2016. Results: The mean age of patients was 34.3 years. Breast lump was the most common presentation. The right breast was affected in 30 cases & left breast 20 cases. 4 patients were pregnant at the time of presentation. Lactation within 6 months of presentation was documented in 4patients.45 patients used contraceptives pills. A clinical suspicion of malignancy was present in 17 cases. Mammography was performed in 20 patients and showed focal asymmetrical dense lesions in 9, well-circumscribed opacity in 8, speculated lesion in 1, and was normal in 2. Fine-needle aspiration was performed in 40 patients. Wide local excision was the mainstay of treatment. One patient underwent mastectomy due to recurrence and the final histology confirmed idiopathic granulomatous mastitis with no evidence of malignancy. 12 patients developed recurrence after a mean follow-up of 31.2 months. Conclusion: IGM is not so rare disease in our country. Clinical, radiologic, and even cytological findings are sometimes confused with malignancy. Adequate Surgical treatment as well as adjuvant therapeutic treatment are necessary. Knowledge, awareness and co-operation among surgeons and pathologist should also be strengthen to avoid unnecessary misdiagnosis and treatment. Journal of Surgical Sciences (2017) Vol. 21 (2): 89-93
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