Ductus Arteriosus Aneurysm with Massive Thrombosis of Pulmonary Artery and Fetal Hydrops

Author:

Sheridan Rachel M.1,Michelfelder Erik C.2,Choe Kyuran A.3,Divanovic Allison2,Liu Cong4,Ware Stephanie4,Stanek Jerzy1

Affiliation:

1. Division of Pathology and Laboratory Medicine, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, MLC 1010, Cincinnati, OH 45229-3039, USA

2. Fetal Heart Program, The Heart Institute, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, MLC 2003, Cincinnati, OH 45229-3039, USA

3. Department of Radiology, University of Cincinnati College of Medicine, 234 Goodman Street, Cincinnati, OH 45219, USA

4. The Heart Institute, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, MLC 7020, Cincinnati, OH 45229-3039, USA

Abstract

Ductus arteriosus aneurysm (DAA) is a rare cardiovascular lesion usually diagnosed within the first 2 months of life, or less frequently in the 3rd trimester, by antenatal sonography. The true in utero incidence of DAA is unknown, as most affected fetuses are asymptomatic at birth. Potential complications include thromboembolism, rupture, and death. We report a unique lethal case of a large DAA detected by mid–2nd trimester fetal echocardiography, complicated by stricture and massive occlusive thrombosis extending into the pulmonary artery branches. Stricture and thrombosis of the DAA led to interruption of fetal circulation, cardiac failure, and fetal hydrops, ultimately resulting in fetal demise.

Publisher

SAGE Publications

Subject

General Medicine,Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health

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