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首页> 外文期刊>Journal of Clinical and Diagnostic Research >Invasive Cystic Hypersecretory Carcinoma of Breast: A Rare and Under Diagnosed Variant of Ductal Carcinoma ED16-ED17
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Invasive Cystic Hypersecretory Carcinoma of Breast: A Rare and Under Diagnosed Variant of Ductal Carcinoma ED16-ED17

机译:乳腺浸润性囊性高分泌性癌:导管癌ED16-ED17的一种罕见且诊断不足的变体

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摘要

Handful cases of invasive Cystic Hypersecretory Ductal Carcinoma (CHC) have been reported so far in literature. Cystic hypersecretory lesions of breast have a spectrum of morphological features ranging from Cystic Hypersecretory Hyperplasia (CHH), CHH with atypia, in situ to invasive CHC. We are reporting a case of a 32-year-old female who had nipple discharge and lump in her right breast for one month. A modified radical mastectomy was done and morphological diagnosis of invasive CHC with axillary node metastasis was made. The postoperative events were uneventful. Invasive CHC being a rare entity, our understanding of its biological behavior, prognostic factors and genetic basis is limited. The authors are aware of only 15 similar cases being reported in the English literature.
机译:迄今为止,文献中已经报道了少数侵袭性囊性高分泌性导管癌(CHC)病例。乳腺的囊性高分泌性病变具有一系列形态学特征,范围从囊性高分泌性增生(CHH),非典型性CHH到浸润性CHC。我们正在报告一例32岁的女性,她的右乳房有乳头溢液和肿块,持续了一个月。进行了改良的根治性乳房切除术,并对具有腋窝转移的浸润性CHC进行了形态学诊断。术后事件进展顺利。侵入性CHC是一种罕见的实体,我们对其生物学行为,预后因素和遗传基础的了解有限。作者意识到英语文献中仅报道了15个类似案例。

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