Prenatal diagnosis and pregnancy outcome of acardiac amorphus twin
Mahdi Farhati, Abir Karoui
Corresponding author: Mahdi Farhati, Tunis Maternity and Neonatology Center, Tunis, Tunisia
Received: 03 Apr 2022 - Accepted: 13 Apr 2022 - Published: 05 May 2022
Domain: Obstetrics and gynecology
Keywords: Twin reversed arterial perfusion, ultrasound, prenatal diagnosis
©Mahdi Farhati et al. Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Cite this article: Mahdi Farhati et al. Prenatal diagnosis and pregnancy outcome of acardiac amorphus twin. Pan African Medical Journal. 2022;42:5. [doi: 10.11604/pamj.2022.42.5.34633]
Available online at: https://www.panafrican-med-journal.com//content/article/42/5/full
Prenatal diagnosis and pregnancy outcome of acardiac amorphus twin
&Corresponding author
We report a case of a 35 years old primigravida patient, referred at 17 weeks of gestation to our consultation for suspicion of a twin pregnancy with vanishing twin. Ultrasound exam showed one fetus with appropriate for gestational age dimensions next to an amorphus mass of 59 mm (A,B). A reversal in arterial flow was noted on a Doppler study, coming from the apparently normal fetus to the mass, and the diagnosis of acardiac twin was made. In view of the absence of negative ultrasound signs (umbilical artery PI ratio, umbilical artery RI differences, weight ratio between acardiac mass and pump twin, heart function of pump twin and amniotic fluid volume) we decided to follow the pregnancy by fortnightly ultrasound checks. At 29 weeks of gestation, a bilateral ventriculomegaly was discovered at the cephalic level without any signs of heart decompensation. A fetal brain MRI was performed at 32 weeks of gestation and showed porencephaly and schizencephaly lesions related to anoxischemic and hemorrhagic sequelae. Intra-uterine fetal death occurred at 32 weeks of gestation. The examination after evacuation showed a stillborn of 1800g of normal morphology, an amorphous acardiac fetus with an outline of a limb weighing 200g (C).
Figure 1: acardiac amorphus twin