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Collagen Type III alpha1 as a useful diagnostic immunohistochemical marker for fibroepithelial lesions of the breast
Phyllodes tumors of the breast constitute an uncommon group of fibroepithelial neoplasms that are classified into benign, borderline and malignant categories based on a constellation of histological characteristics including cytologic atypia, mitotic count, degree of stromal cellularity, stromal ove...
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Published in: | Human pathology 2016 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Phyllodes tumors of the breast constitute an uncommon group of fibroepithelial neoplasms that are classified into benign, borderline and malignant categories based on a constellation of histological characteristics including cytologic atypia, mitotic count, degree of stromal cellularity, stromal overgrowth, and microscopic margins. Accurately and reproducibly differentiating these tumors is a long-standing diagnostic challenge. In addition, the distinction between benign phyllodes tumor (PT) from cellular fibroadenoma (FA) is especially difficult due to overlapping microscopic features. We have previously shown differential expression of various collagens, including collagen type III alpha1 (Col3A) in breast carcinomas. In this study, we evaluated clinicopathologic characteristics of 95 cases of fibroepithelial lesions including 56 PTs and 39 FAs (25 cellular FA, 14 typical FA) and correlated them with the immunohistochemical staining pattern for Col3A. We found that stromal Col3A expression was significantly increased in PTs when compared to FAs (P < .0001). Among the PT groups, there was significantly increased expression from benign tumors through borderline to malignant tumors. High Col3A expression was associated with PT type, irregular margin status and high mitotic activity. A distinct periductal cuffing pattern of Col3A staining was unique to PTs and absent in FAs. These findings suggest that Col3A can be a potential adjunct marker for both differentiating FA from PT and assessing malignant potential in PTs. |
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ISSN: | 0046-8177 |
DOI: | 10.1016/j.humpath.2016.07.017 |