| Literature DB >> 21340004 |
Emanuela Anastasi1, Teresa Granato, Anna Coppa, Lucia Manganaro, Giuseppe Giannini, Sara Comploj, Luigi Frati, Cecilia Midulla.
Abstract
Neoplasms of the ovary present an increasing challenge to the physician. Neoplastic ovarian cysts can resemble endometriomas in ultrasound imaging and need to be carefully considered in the differential diagnosis. We report the case of a woman with a strong family history of hereditary breast and ovarian cancer, who presented with a pelvic mass. The young girl refused oncogenetic counseling and genetic testing, even though she had a 50% a priori probability of being a BRCA1 mutation carrier. Pelvic magnetic resonance imaging (MRI) and a comparative analysis of the serum concentration of HE-4 and CA125 biomarkers provided accuracy and sensitivity in the diagnosis of a benign ovarian pathology. Based on this experience, we propose that the sensitivity of a screening program based on a HE4 and CA125 assay and MRI in high risk patients with mutations in the BRCA1 and BRCA2 genes may be considered a useful pre-operative tool for the differential diagnosis of pelvic masses.Entities:
Keywords: HE4 tumor marker; endometriosis; high-risk patients; ovarian cancer
Mesh:
Substances:
Year: 2011 PMID: 21340004 PMCID: PMC3039970 DOI: 10.3390/ijms12010627
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923
Figure 1Genealogical diagram of the family with indication of the subjects mutated and the type of cancers.
Figure 2Transvaginal pelvic ultrasound shows cystic structures with low level internal echoes and echogenic wall foci, thickened walls and septations.
Figure 3T2 TSE weighed sequences. Complex images in the left ovary, fluid/fluid level, hypointense images in the declive position, axially.
Figure 4T1 VIBE weighed sequences. Marked hyperintense signal observed in the left ovary and a weakly hyperintense thin area is observed in the posterior uterine wall, referred to as an endometril implant.
CA125 (expressed as U/mL) and HE4 (expressed as pmol/L) levels, evaluated at a two different times (the first at the moment of the gynecologic examination and the second two weeks later).
| Sample 1 | Sample 2 | |
|---|---|---|
| 185 | 330 | |
| 44 | 40 |