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The acardiac twin malformation, historically viewed with superstition, is now understood as twin reversed arterial perfusion and can be treated with prenatal radiofrequency ablation.
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This historical review traces the evolution of medical understanding of twin reversed arterial perfusion sequence from ancient superstition to modern interventional management.
A human being born without heart and head, i.e., the acardius/acranius malformation, has been described since antiquity. Superstition and fear made it a mystical disorder, a sign of God's wrath. The inquisition ruled that acranic infants should not be baptized and located the soul in the brain. Acardia was not associated with twin gestation until the reports of Mery in 1720 and Winslow in 1740. In 1850, Meckel identified the pathogenetic mechanism as reversed perfusion due to large arterio-arterial and veno-venous anastomoses; he believed the heart would fail to develop or arrest during development, and the acardiac fetus would be maintained by arterial perfusion from the pump twin. In 1859, Claudius articulated that after normal initial development, the heart degenerates when reversed flow in the aorta leads to thrombosis. Today, it is assumed that both mechanisms may exist. With the advent of prenatal ultrasound diagnosis and radiofrequency ablation of the acardiac twin's circulation, it became possible to save the pump twin.
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Michael Obladen (2010) conducted a review in Acardiac twins / Twin reversed arterial perfusion. The acardiac twin malformation, historically viewed with superstition, is now understood as twin reversed arterial perfusion and can be treated with prenatal radiofrequency ablation.
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