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KMID : 1039420190530040236
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Journal of Pathology and Translational Medicine
2019 Volume.53 No. 4 p.236 ~ p.243
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Serous Adenocarcinoma of Fallopian Tubes: Histological and Immunohistochemical Aspects
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Hyriavenko Natalia
Lyndin Mykola
Sikora Kateryna
Piddubnyi Artem
Karpenko Ludmila
Kravtsova Olha
Hyriavenko Dmytrii
Diachenko Olena
Sikora Vladyslav
Romaniuk Anatolii
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Abstract
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Background: Although primary cancer of the fallopian tubes is a relatively rare type of tumor in female reproductive organs, its mortality is quite high. It is important to identify molecular and biological markers of this malignancy that determine its specific phenotype.
Methods: The study was carried out on samples received from 71 female patients with primary cancer of the fallopian tubes. The main molecular and biological properties, including hormone status (estrogen receptor [ER], progesterone receptor [PR]), human epidermal growth factor receptor (HER2)/neu expression, proliferative potential (Ki-67), apoptosis (p53, Bcl-2), and pro-angiogenic (vascular endothelial growth factor) quality of serous tumors were studied in comparison with clinical and morphological characteristics.
Results: ER and PR expression is accompanied by low grade neoplasia, early clinical disease stage, and absence of lymphogenic metastasis (p < .001). HER2/neu expression is not typical for primary cancer of the fallopian tubes. Ki-67 expression is characterized by an inverse correlation with ER and PR (p < .05) and is associated with lymphogenic metastasis (p < .01). p53+ status correlates with high grade malignancy, tumor progression, metastasis, negative ER/PR (p < .001), and negative Bcl-2 status (p < .05). Positive Bcl-2 status is positively correlated with ER and PR expression and low grade malignancy.
Conclusions: Complex morphologic (histological and immunohistochemical) study of postoperative material allows estimation of the degree of malignancy and tumor spread to enable appropriate treatment for each case.
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KEYWORD
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Carcinoma, serous, Neoplasms, Fallopian tubes, Estrogen receptor, Progesterone receptor, Ki-67, HER2/neu
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