Abstract
Nuclear Inverse Polarity Papillary Lesions with Lack Myoepithelial Cells: A Report of Two Cases
Shinya Tajima*, Nobuhiko Matsumoto, Motohiro Chosokabe, Akira Endo, Saeko Naruki, Masatomo Doi, Keiko Kishimoto, KoichiroTsugawa, Masayuki Takagi and Junki Koike
Corresponding Author: Shinya Tajima, Department of Pathology, St. Marianna University School of Medicine, 2-16-1 Sugao, Miyamae-ku, Kawasaki city, Kanagawa prefecture, 216-8511, Japan
Revised: September 20, 2020 ; Available Online: October 07, 2020
Citation: Tajima S, Matsumoto N, Chosokabe M, Endo A, Naruki S, et al. (2020) Nuclear Inverse Polarity Papillary Lesions with Lack Myoepithelial Cells: A Report of Two Cases. Food Nutr Current Res, 3(S1): 14.
Copyrights: ©2020 Tajima S, Matsumoto N, Chosokabe M, Endo A, Naruki S, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Breast cancer is world-threatening disease. In Japan, it is said that 1 person for 11 people diagnosed breast cancer. Hence, early detection of breast cancer and healthy lifestyle is important. pocrine” papillary lesions lacking myoepithelial cells associated with interesting immunohistochemistry results and clinico-pathological features. Both papillary lesions were lined by a fibrovascular core and nuclear inverse polarity without nuclear atypia. Loss of myoepithelial cells was observed by H&E, p63 and Calponin stainings. Some reports have indicated that high-molecular-weight cytokeratin (CK) 5/6 and estrogen receptor (ER) immunostainings are important for differentiating benign versus malignant lesions. Moreover, previous report indicate p63 and MUC3 are important for distinguishing between papillary lesions according to the differential index (based on the Allred score) of ([ER total score] + [MUC3 total score])/([CK5/6 total score] + [p63 total score] + 1). Based on this analysis, our 2 cases had benign lesions. However, for the cell-cycle marker Cyclin-D1, one case was negative, and the other case was about weak 70% positive. Additionally, the Ki-67 index was <<1% in both cases, and no evidence of disease was observed at least 62 months of follow-up for both cases, despite a lack of additional treatment. Thus, we propose that lack of myoepithelial cells in nuclear inverse polarity papillary lesions do not necessarily indicate malignancy and that the present cases are clinically benign however histologically at the most tumors of uncertain malignant potential. Therefore, we should carefully diagnose the breast papillary lesions even if lacking myoepithelial cells.

Keywords: Apocrine lesions, Tumors, Breast papillary lesions, Malignant lesions
 
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