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首页> 外文期刊>Pathology International >Double neuroendocrine ductal carcinomas in situ coexisting with a background of diffuse idiopathic neuroendocrine cell hyperplasia of breast: A case report and hypothesis of neuroendocrine tumor development
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Double neuroendocrine ductal carcinomas in situ coexisting with a background of diffuse idiopathic neuroendocrine cell hyperplasia of breast: A case report and hypothesis of neuroendocrine tumor development

机译:乳腺弥漫性特发性神经内分泌细胞增生的背景下原位并存双神经内分泌导管癌:一例神经内分泌肿瘤发展的病例报道及假设

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摘要

This article reports the case of a 72-year-old woman with two nodules of neuroendocrine (NE) ductal carcinoma in situ coexistent with a background of NE cell hyperplasia. Both tumors, 15 and 3mm in size, were incidentally revealed on computed tomography without any apparent clinical symptoms. The tumors showed similar histological features, and more than 50% of the tumor cells patchily expressed NE markers, such as chromogranin A, synaptophysin, CD56, and somatostatin receptor type 2. The surrounding nontumor ductal cells also showed spotty or linear positivity for NE markers in contrast to the cells of normal atrophic breasts, which rarely present with NE cells. Moreover, focal mucin production was also observed in the peripheral ducts. It is hypothesized that idiopathic breast NE cell hyperplasia with multiple small nests of NE cells may extend to form a true mass of NE neoplasms.
机译:本文报道一例72岁女性,原位并发神经内分泌(NE)导管癌两个结节,并伴有NE细胞增生。在计算机断层扫描上偶然发现了大小分别为15和3mm的两种肿瘤,没有任何明显的临床症状。肿瘤表现出相似的组织学特征,超过50%的肿瘤细胞修补表达NE标志物,例如嗜铬粒蛋白A,突触素,CD56和生长抑素受体2型。周围的非肿瘤导管细胞也显示NE标志物斑点或线性阳性与正常萎缩性乳房细胞相比,后者很少出现NE细胞。此外,在外周管中也观察到局灶性粘蛋白产生。假设特发性乳腺NE细胞增生伴有NE细胞的多个小巢,可能会扩展形成真实数量的NE肿瘤。

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