CC BY-NC-ND 4.0 · AJP Rep 2020; 10(02): e176-e178
DOI: 10.1055/s-0040-1709981
Case Report
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Cell-Free DNA as an Addition to Ultrasound for Screening of a Complete Hydatidiform Mole and Coexisting Normal Fetus Pregnancy: A Case Report

1   Department of Obstetrics and Gynecology, Banner-University Medical Center, University of Arizona, Tucson, Arizona
,
Maritza G. Gonzalez
1   Department of Obstetrics and Gynecology, Banner-University Medical Center, University of Arizona, Tucson, Arizona
,
Holly N. Bullock
1   Department of Obstetrics and Gynecology, Banner-University Medical Center, University of Arizona, Tucson, Arizona
,
Meghan G. Hill
1   Department of Obstetrics and Gynecology, Banner-University Medical Center, University of Arizona, Tucson, Arizona
› Author Affiliations
Funding None.
Further Information

Publication History

05 February 2020

20 February 2020

Publication Date:
18 June 2020 (online)

Abstract

Background Complete hydatidiform mole and coexisting normal fetus pregnancies (CHMCF) are rare and can be life-threatening to the mother. Definitive diagnosis can be made with chorionic villus sampling or amniocentesis. However invasive procedures carry a risk of bleeding. We present the case of a twin molar pregnancy where a cell-free DNA screening test was utilized to evaluate for CHMCF pregnancy.

Case A patient presented at 15-week gestational age with suspected CHMCF pregnancy. Ultrasound revealed a normal-appearing pregnancy abutting a multicystic lesion concerning for a complete mole. Cell-free DNA was obtained and was suggestive of complete paternal uniparental disomy. Pathological evaluation of the products of conception confirmed the diagnosis of CHMCF.

Conclusion In atypical cases, cell-free DNA may be useful in evaluation of molar pregnancy.

Note

Patient consent was obtained for publication of this article.


 
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