RESEARCH ARTICLE
A Case of Poorly Differentiated Squamous Cell Carcinoma in the Breast: A Thorough Investigation of its Origins
Fumie Shono1, 4, Shigeki Inui*, 4, Satoshi Takagi1, Kazuya Kuraoka2, Kiyomi Taniyama2, Shinichi Ansai3, Tetsunori Kimura3
Article Information
Identifiers and Pagination:
Year: 2010Volume: 4
First Page: 105
Last Page: 107
Publisher ID: TODJ-4-105
DOI: 10.2174/1874372201004010105
Article History:
Received Date: 26/05/2010Revision Received Date: 23/08/2010
Acceptance Date: 09/10/2010
Electronic publication date: 11/10/2010
Collection year: 2010
open-access license: This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: https://creativecommons.org/licenses/by/4.0/legalcode. This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
An 81-year-old female consulted us because of an ulcerated tumor in her left breast of several years' duration. Partial biopsy showed that the tumor consisted of anaplastic squamous cells, indicating squamous cell carcinoma from unknown origin. CT images demonstrated tumors in the left breast, liver and bile duct. However, further investigation was not possible due to the patient's refusal. To avoid possible localized complication caused by tumor rupture and/or infection, the breast tumor was totally excised. Histopathology revealed that irregularly shaped tumor nests had invaded the entire dermis resulting in massive necrosis. The tumor cells were of various sizes and shapes, and showed individual keratinization and atypical mitotic figures. In addition, other larger masses consisted of hyperchromatic small squamous cells with basophilic cytoplasms. These cells were poorly differentiated without apparent keratinization. Immunohistochemically, the excised tumor was stained strongly positive for epidermal growth factor receptor, partially positive for epithelial membrane antigen and BerEP4 but negative for cytokeratins 5, 6 and 20, estrogen receptor, progesterone receptor, ErbB2/HER2, gross cystic disease fluid protein-15, carcinoembryonic antigen and S-100. Since these findings were not sufficient to identify the tumor origin, we carefully rechecked the histopathology of the surgical specimens and found irregular elongation at the periphery of the overlying epidermis, which contained atypical keratinocytes with pleomorphic nuclei, suggesting a diagnosis of Bowen's disease. We therefore concluded that tumor cells of Bowen's disease in the epidermis, independently from the tumors of liver and bile duct, had invaded downward, finally reaching the breast tissue.