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伴有派杰样扩散及淋巴结转移的乳头浸润性实性乳头状癌

Invasive Solid Papillary Carcinoma of the Nipple With Pagetoid Extension and Nodal Metastasis.

作者信息

Domoto Hideharu, Watanabe Akiko, Sakata Michio, Shimada Akihiko, Mukai Kiyoshi

机构信息

1 Keiyu Hospital, Yokohama, Japan.

出版信息

Int J Surg Pathol. 2018 Sep;26(6):573-577. doi: 10.1177/1066896918766237. Epub 2018 Mar 27.

DOI:10.1177/1066896918766237
PMID:29580118
Abstract

We report a case of invasive solid papillary carcinoma (SPC) of the nipple with Pagetoid extension to the skin and lymph node metastasis. SPC is an uncommon primary breast cancer accounting for less than 1% of all breast cancers. Only 2 cases occurring in the nipple have been reported. However, both cases were without Pagetoid extension or lymph node metastasis. The presently reported tumor consisted of irregularly shaped solid cell nests with delicate fibrovascular cores. The tumor cells had round nuclei with low-grade atypia and eosinophilic cytoplasm. Neuroendocrine differentiation was confirmed by immunohistochemical positivity for CD56, synaptophysin, and chromogranin A. Immunohistochemistry also confirmed the absence of myoepithelial cells around the tumor cell nests. Therefore, a diagnosis of invasive SPC was made. Additionally, tumor cell deposits in the intramammary and axillary lymph nodes were identified, and these deposits had the same histological characteristics as the invasive SPC of the nipple. The invasiveness of SPC can be difficult to determine. However, the tumor cell nests in the current case exhibited a retraction artifact, which is known to be associated with invasive carcinoma and a poor prognosis, as well as morphological patterns that have been previously identified as characteristic of invasive SPC. Although SPC is widely recognized as having a favorable outcome, the existence of exceptionally aggressive cases occurring in the nipple must be recognized. Additional cases of invasive SPC of the nipple are needed to analyze the clinicopathological correlation.

摘要

我们报告一例乳头浸润性实性乳头状癌(SPC),伴有派杰样皮肤浸润及淋巴结转移。SPC是一种罕见的原发性乳腺癌,占所有乳腺癌的比例不到1%。仅报道过2例发生于乳头的病例,但这两例均无派杰样浸润或淋巴结转移。目前报道的肿瘤由形状不规则的实性细胞巢组成,伴有纤细的纤维血管轴心。肿瘤细胞具有圆形核,异型性低,胞质嗜酸性。免疫组化显示CD56、突触素和嗜铬粒蛋白A阳性,证实有神经内分泌分化。免疫组化还证实肿瘤细胞巢周围不存在肌上皮细胞。因此,诊断为浸润性SPC。此外,在乳腺内及腋窝淋巴结中发现了肿瘤细胞沉积物,这些沉积物具有与乳头浸润性SPC相同的组织学特征。SPC的浸润性可能难以确定。然而,本例中的肿瘤细胞巢出现了退缩假象,已知这与浸润性癌及预后不良相关,同时还具有先前已确定为浸润性SPC特征的形态学模式。尽管SPC普遍被认为预后良好,但必须认识到乳头部位存在具有异常侵袭性的病例。需要更多乳头浸润性SPC病例来分析临床病理相关性。

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引用本文的文献

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Surg Case Rep. 2020 Jun 19;6(1):143. doi: 10.1186/s40792-020-00905-x.