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首页> 外文期刊>Acta Cytologica: The Journal of Clinical Cytology and Cytopathology >Idiopathic granulomatous mastitis - Report of a case diagnosed with fine needle aspiration cytology
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Idiopathic granulomatous mastitis - Report of a case diagnosed with fine needle aspiration cytology

机译:特发性肉芽肿性乳腺炎-细针穿刺细胞学诊断病例报告

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摘要

BACKGROUND: Idiopathic granulomatous mastitis (IGM) is a benign, inflammatory breast disease of unknown etiology. Although it is rare, it frequently presents in a manner similar to that of breast carcinoma. CASE: A 41-year-old female developed unilateral idiopathic granulomatous mastitis, diagnosed by fine needle aspiration cytology. The clinical presentation and mammographic findings were suspicious for carcinoma. Fine needle aspiration cytology showed granulomatous inflammation. Histopathologic examination revealed a noncaseating, granulomatous lesion. Further clinical, radiologic and laboratory investigations disclosed no etiology. Therefore, we considered the case to be idiopathic granulomatous mastitis. CONCLUSION: Cytologically it may be difficult to distinguish IGM from carcinoma of the breast. Typical cytologic findings of the lesion are helpful to rule out cancer. In the differential diagnosis, all known causes of granulomatous changes have to be excluded before a diagnosis of idiopathic granulomatous mastitis is made. [References: 8]
机译:背景:特发性肉芽肿性乳腺炎(IGM)是一种病因不明的良性,炎性乳腺疾病。尽管很少见,但经常以类似于乳腺癌的方式出现。病例:一名41岁女性患上单侧特发性肉芽肿性乳腺炎,经细针穿刺细胞学检查确诊。临床表现和乳房X线照片可疑为癌。细针穿刺细胞学检查显示肉芽肿性炎症。组织病理学检查显示无干酪样肉芽肿病灶。进一步的临床,放射学和实验室检查未发现病因。因此,我们认为该病例是特发性肉芽肿性乳腺炎。结论:从细胞学上讲,可能很难区分IGM和乳腺癌。病变的典型细胞学检查结果有助于排除癌症。在鉴别诊断中,必须在诊断出特发性肉芽肿性乳腺炎之前排除所有已知的肉芽肿性改变的原因。 [参考:8]

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