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男性乳腺高核级囊内乳头状癌:一例报告

Intracystic Papillary Carcinoma in Male Breast with High Nuclear Grade: A Case Report.

作者信息

Al Salloom Abdulaziz Ajlan M

机构信息

Consultand and Assistant Professor, Department of Pathology, College of Medicine, Qassim University , Buraidah, KSA, Saudi Arabia .

出版信息

J Clin Diagn Res. 2015 Aug;9(8):ED04-5. doi: 10.7860/JCDR/2015/13909.6299. Epub 2015 Aug 1.

Abstract

Intracystic papillary carcinoma (IPC) in men is an extremely rare disease that accounts for less than 1% of all malignancies with only a few case presentations published so far. This report presents a case of 53-year-old male, who presented a painless swelling of his left breast. The left breast mass was 6 cm maximally and was found to be non-invasive IPC. The tumour is consistently positive for GCDFP-15, ER or PR and negative for HER-2. It consists of predominantly fibrovascular stromal lined by monotonous epithelial cells retaining intermediate to high histological grade with a high nuclear cytoplasmic ratio. In addition, increased numbers of mitotic figures were also seen. Chest X-ray, liver ultrasound and bone centigram showed no evidence of distant metastases. In short, this is the first case report from Saudi Arabia of a male having IPC, with increased number of mitotic figures and high nuclear grades.

摘要

男性囊内乳头状癌(IPC)是一种极为罕见的疾病,占所有恶性肿瘤的比例不到1%,迄今为止仅有少数病例报告发表。本报告介绍了一名53岁男性病例,该患者左侧乳房出现无痛性肿胀。左侧乳房肿块最大为6厘米,被诊断为非浸润性IPC。肿瘤GCDFP - 15、雌激素受体(ER)或孕激素受体(PR)持续呈阳性,人表皮生长因子受体2(HER - 2)呈阴性。它主要由纤维血管间质构成,内衬单调的上皮细胞,组织学分级为中到高,核质比高。此外,还可见有丝分裂象数量增加。胸部X线、肝脏超声和骨X线检查均未发现远处转移迹象。简而言之,这是沙特阿拉伯首例关于男性患IPC且有丝分裂象数量增加和核分级高的病例报告。

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本文引用的文献

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"Intracystic papillary breast cancer: a clinical update".囊内乳头状乳腺癌:临床最新进展
Ecancermedicalscience. 2013;7:286. doi: 10.3332/ecancer.2013.286. Epub 2013 Jan 3.
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Invasive papillary carcinoma of male breast.男性乳腺浸润性乳头状癌。
Indian J Pathol Microbiol. 2010 Jan-Mar;53(1):135-7. doi: 10.4103/0377-4929.59206.
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Breast intracystic papillary carcinoma: an update.乳腺囊内乳头状癌:更新。
Breast J. 2009 Nov-Dec;15(6):639-44. doi: 10.1111/j.1524-4741.2009.00823.x. Epub 2009 Sep 7.

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