Krukenberg tumor in pregnancy: a rare case and review of the literature

IG Goidescu, G Nemeti, A Preda, T Kovacs… - The Journal of …, 2022 - Taylor & Francis
Krukenberg's tumor diagnosed in pregnancy is an uncommon situation that raises both
diagnosis and medical management issues. We performed a review of the existing literature …

The role of imaging techniques in the diagnosis, staging and choice of therapeutic conduct in pregnancy associated breast cancer

I Goidescu, G Nemeti, G Caracostea… - Medical …, 2019 - medultrason.ro
Breast cancer diagnosed during pregnancy is at increasing incidence due to the increased
frequency of obesity, the postponement of the first pregnancy to later decades of life and the …

[HTML][HTML] Prevalence of deleterious mutations among patients with breast cancer referred for multigene panel testing in a Romanian population

IG Goidescu, G Caracostea, DT Eniu… - Clujul Medical, 2018 - ncbi.nlm.nih.gov
Prevalence of deleterious mutations among patients with breast cancer referred for multigene
panel testing in a Romanian population - PMC Back to Top Skip to main content NIH NLM …

[PDF][PDF] Do we really need genetic tests in current clinical practice?

C Bănescu - Revista Romana de Medicina de Laborator, 2019 - sciendo.com
Currently there is an increased number of genetic tests available for disorders produced by
chromosomal or gene abnormalities. Some genetic tests are recommended by healthcare …

Mutational landscape of BRCA gene mutations in Indian breast cancer patients: retrospective insights from a diagnostic lab

R Chikkala, D Bhayal, N Rani, R Modali… - Egyptian Journal of …, 2024 - Springer
Abstract Background Presence of Germline mutations in the BRCA 1 and BRCA 2 genes is
the most significant epidemiological factor for breast cancer (BC), where germline BRCA1 (g …

Spectrum of High-Risk Mutations among Breast Cancer Patients Referred for Multigene Panel Testing in a Romanian Population

IG Goidescu, G Nemeti, M Surcel, G Caracostea… - Cancers, 2023 - mdpi.com
Simple Summary Multigene panel testing for Hereditary Breast and Ovarian Cancer using
next generation sequencing is the new standard for the identification of individuals with …

[PDF][PDF] Blue nevus-like melanoma of the uterine cervix. Case report and review of the literature

DT Eniu, A Staicu, O Somcutian, R Buiga… - Rom J Morphol …, 2019 - researchgate.net
We present the clinical and pathological aspects of a patient diagnosed with a very rare
tumor, a blue nevus-like melanoma of the uterine cervix. The patient turned to our Service for …

Histopathological characterization of carcinoma breast with BRCA1/2 sequence variation in a tertiary care center in Kerala, South India

RM Issac, P Saldanha, JM Mathai… - Biomedical and …, 2022 - journals.lww.com
Background: Hereditary breast cancers constitute around 5%–10% of all breast cancers.
The most commonly mutated genes in hereditary breast and ovarian cancer syndrome are …

[PDF][PDF] The influence of reproductive factors on breast cancer risk in women with pathogenic mutations

IG Goidescu, G Caracostea, IC Rotar, DT Eniu… - J BUON, 2019 - researchgate.net
Purpose: To assess the influence of reproductive factors in the occurrence of breast cancer
in women, taking into account the presence/absence of genetic predisposing mutations …

High frequency of BRCA recurrent mutations in a consecutive series of unselected ovarian cancer patients

A Chicos, L Negura, R Braescu, A Morariu… - Revista Romana de …, 2020 - sciendo.com
Hereditary predisposition to breast and ovarian cancer (HBOC) is diagnosed by molecular
analysis of deleterious mutations in BRCA genes, allowing oncogenetic follow-up of patients …