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Eosinophilic Cells in Ovarian Borderline Serous Tumors as a Predictor of BRAF Mutation
According to recent reports, ovarian serous borderline tumor (SBT) harboring the V600E mutation is associated with a lower risk of progression to low-grade serous carcinoma. Preliminary observations suggest that there may be an association between eosinophilic cells (ECs) and the above-mentioned mut...
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Published in: | Cancers 2024-06, Vol.16 (13), p.2322 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | According to recent reports, ovarian serous borderline tumor (SBT) harboring the
V600E mutation is associated with a lower risk of progression to low-grade serous carcinoma. Preliminary observations suggest that there may be an association between eosinophilic cells (ECs) and the above-mentioned mutation, so this study aimed to evaluate interobserver reproducibility for assessing ECs. Forty-two samples of SBTs were analyzed for ECs with abundant eosinophilic cytoplasm. Immunohistochemical staining and genetic pro-filing were performed in all cases to verify the
V600E mutation. A
V600E mutation was found in 19 of 42 (45%) cases. Inter-observer reproducibility in the assessment of ECs was substantial (κ = 0.7). The sensitivity and specificity for predicting the mutation were 79% and 91%, respectively. Patients with
-mutated SBTs were significantly younger than those without mutation (
= 0.005). SBTs with
mutation were less likely to be accompanied by non-invasive implants than wild-type SBT: 12% (2/17) versus 33% (6/18). Seven cases were excluded due to incomplete cytoreductive surgery. Nevertheless, Fisher's exact test showed no significant differences between the two groups (
= 0.228). Overall, this study strengthens the idea that ECs in ovarian SBTs may represent a mutation with prognostic significance, which can serve as a primary screening test for
V600E mutation in this pathologic entity. |
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ISSN: | 2072-6694 2072-6694 |
DOI: | 10.3390/cancers16132322 |