肉芽肿性乳腺炎
医学
病因学
疾病
皮肤病科
组织病理学
乳腺炎
病理
乳腺癌
自身免疫
免疫学
癌症
内科学
作者
Yulong Yin,Xianghua Li,Qi Meng,Xiaogang Han,Haomeng Zhang,Yonggang Lv
标识
DOI:10.1080/08941939.2021.1894516
摘要
Idiopathic granulomatous mastitis (IGM) is a rare form of chronic inflammatory breast disease. Although it is a benign breast lesion, it may be sometimes difficult to distinguish from breast cancer. The cause of IGM is unknown, but may be associated with autoimmunity, abnormal hormone levels and infection. While the clinical manifestations of IGM involve various manifestations of inflammation, the diagnosis is principally established by histopathology, characterized by non-caseating granulomas and microabscess formation centered on the breast lobules. Therapeutic options for IGM range from observation to various medical treatments, such as steroids, immunosuppressants, and antibiotics, to surgical intervention, particularly if secondarily infected. Given that the controversy on etiology and treatment choices, we accomplished the present review through reviewing IGM-related literature published in 'Pubmed' and 'Web of science' databases during 1997 to 2020, aiming to provide the basis for rational clinical diagnosis and treatment.
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