Prenatal diagnosis, management, and postnatal outcome of a fetus with massive cardiomegaly secondary to placenta chorioangioma.

Autor: Karmegaraj B; Department of Pediatric Cardiology, Amrita Institute of Medical Sciences and Research Centre, Amrita University, Kochi, Kerala, India.; Sowmi Fetal & Pediatric Heart Centre, Tirunelveli, Tamilnadu, India.; Department of Pediatrics, Royal Hospital, Tirunelveli, Tamilnadu, India., Ibrahim S; Department of Pediatrics, Royal Hospital, Tirunelveli, Tamilnadu, India., Razeen M; Department of Pediatrics, Royal Hospital, Tirunelveli, Tamilnadu, India., Premasudha V; Department of Obstetrics and Gynecology, Royal Hospital, Tirunelveli, Tamilnadu, India., Rajesh A; Department of Pathology, Muthamil Hospital, Tirunelveli, Tamilnadu, India.
Jazyk: angličtina
Zdroj: Echocardiography (Mount Kisco, N.Y.) [Echocardiography] 2022 Jan; Vol. 39 (1), pp. 157-161. Date of Electronic Publication: 2021 Dec 18.
DOI: 10.1111/echo.15276
Abstrakt: Chorioangiomas are the most common non-trophoblastic benign vascular tumor of the placenta, highly associated with perinatal death rate. Herewith, we are reporting the prenatal diagnosis, management and postnatal outcome of a fetus referred at 33 weeks gestation with massive cardiomegaly secondary to placenta chorioangioma.
(© 2021 Wiley Periodicals LLC.)
Databáze: MEDLINE
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