Incidental cytokeratin-positive interstitial reticulum cell tumor of the lymph node accompanied by breast cancer: Status of YAP/TAZ expression in tumor cells

Q4 Medicine
Chiemi Saigo , Yusuke Kito , Masayoshi Hasegawa , Shusuke Nomura , Takuya Mikamo , Yuki Hanamatsu , Ryutaro Mori , Manabu Futamura , Kazuhiro Yoshida , Tamotsu Takeuchi
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引用次数: 1

Abstract

Approximately 24 cases of cytokeratin-positive interstitial reticulum cell tumors have been reported in English literature. In this paper, we report a case of cytokeratin-positive interstitial reticulum cell tumor that was localized in the parafollicular region of the axillary lymph node and was an incidental finding in a patient with breast cancer. A 50 year-old woman underwent a mastectomy and lymph node dissection following a preoperative diagnosis of bilateral breast cancer. Histopathological examination revealed that the patient had non-invasive and invasive ductal carcinoma in the right and left mammary glands. Although we could not detect breast cancer metastasis in the lymph nodes, one of eight right axillary lymph nodes harbored an 11 × 8 mm discohesive sheet of large polygonal epithelioid tumor cells in the parafollicular area. Tumor cells were immunoreactive for AE1/AE3, CAM5.2, CK18 and l-caldesmon and negative for CD1a, CD21, CD23, CD31, CD68, and S‑100 protein markers. Based on these findings, the lesion was diagnosed as a cytokeratin-positive interstitial reticulum cell tumor of the lymph node. Notably, this early-stage cytokeratin-positive interstitial reticulum cell tumor demonstrated focal nuclear YAP/TAZ proto-oncogene products, which were recently identified as critical for differentiation, maturation, and function of fibroblastic reticular cells. To the best of our knowledge, this is the first report to describe nuclear YAP/TAZ immunoreactivity in cytokeratin-positive interstitial reticulum cell tumors.

乳腺癌伴发淋巴结偶发细胞角蛋白阳性间质网细胞瘤:YAP/TAZ在肿瘤细胞中的表达状况
在英文文献中报道了大约24例细胞角蛋白阳性间质网细胞瘤。在本文中,我们报告一例细胞角蛋白阳性的间质网细胞肿瘤,该肿瘤位于腋窝淋巴结的滤泡旁区,是一位乳腺癌患者的偶然发现。一位50岁的女性在术前诊断为双侧乳腺癌后接受了乳房切除术和淋巴结清扫。组织病理学检查显示患者在左右乳腺有非浸润性和浸润性导管癌。虽然我们无法在淋巴结中发现乳腺癌转移,但8个右腋窝淋巴结中有一个在滤泡旁区有一个11 × 8 mm的大多边形上皮样肿瘤细胞的不粘连片。肿瘤细胞对AE1/AE3、CAM5.2、CK18和l-caldesmon具有免疫反应,对CD1a、CD21、CD23、CD31、CD68和S - 100蛋白标志物呈阴性。基于这些发现,病灶被诊断为淋巴结细胞角蛋白阳性间质网细胞瘤。值得注意的是,这种早期细胞角蛋白阳性的间质网状细胞肿瘤表现出局灶性核YAP/TAZ原癌基因产物,这些产物最近被发现对成纤维网状细胞的分化、成熟和功能至关重要。据我们所知,这是第一份描述细胞角蛋白阳性间质网细胞肿瘤中细胞核YAP/TAZ免疫反应性的报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Human Pathology: Case Reports
Human Pathology: Case Reports Medicine-Pathology and Forensic Medicine
CiteScore
0.50
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0.00%
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审稿时长
16 weeks
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