Advantages of next-generation sequencing (NGS) in the molecular classification of endometrial carcinomas – our experience with 270 cases
The authors present a case of 1st trimester miscarriage where an early, complete hydatidiform mole was clinically suspected. Histopathological and immunohistochemical analyses excluded a complete mole, but the histomorphological profile was in concordance with a partial hydatidiform mole. Genetic analysis excluded a partial mole based on biparental genome composition, where further genetic analyses detected trisomy of chromosome 16. Trisomy of chromosome 16 is a frequent cause of 1st trimester abortions and may lead to highly abnormal placental histomorphology mimicking a partial mole. Genetic analyses are crucial for proper differential diagnosis and for the determination of adequate follow-up and prognosis for further pregnancies.
Authors
- Petra Priščáková (ORCID: https://orcid.org/0000-0001-7287-3837)
- Ľ Danihel (ORCID: https://orcid.org/0000-0002-6284-4335)
- M Tomka (ORCID: https://orcid.org/0000-0002-5731-9720)
- Vanda Repiská (ORCID: https://orcid.org/0000-0003-1907-8468)
- Miroslav Korbeľ (ORCID: https://orcid.org/0000-0001-8865-9819)
- Liam McCullough (ORCID: https://orcid.org/0009-0002-9237-7472)
- Lajos Gergely (ORCID: https://orcid.org/0000-0003-3407-7914)
Publication Details
- Journal
- Česká gynekologie
- Published
- 2024-10-25
- DOI
- https://doi.org/10.48095/cccg2024396
- Citations
- 1
- Primary Topic
- Prenatal Screening and Diagnostics
- Type
- article
- Field-Weighted Citation Impact
- 1.11