Truncus arteriosus, interrupted aortic arch and amniotic band syndrome are rare conditions. We report a case of a 38-year-old pregnant woman who was diagnosed on a routine morphological ultrasound scan with a Van Praagh type A4 persistent truncus arteriosus with an aortic arch interruption type B and abnormal limbs (oedematous left hand, hypoplastic fingers on the right hand and right big toe amputation). Elective termination of the pregnancy was carried out and the pathological examination confirmed all the sonographic findings. Furthermore, an amniotic band parallel to the umbilical cord undetected during the ultrasound scans was revealed, and was entangled around the right hand, left wrist and the umbilical cord, causing strangulation. We present the unusual association of these independent pathologies and emphasise the usefulness of fetal autopsy in all cases of pregnancy termination and abnormal ultrasound findings to make the complete diagnosis.
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http://dx.doi.org/10.1136/bcr-2020-236049 | DOI Listing |
A A Pract
December 2024
From the Department of Cardiac Anaesthesia, Cardiothoracic Centre, All India Institute of Medical Sciences (AIIMS), New Delhi, India.
Eur Heart J Cardiovasc Imaging
December 2024
M3C CHU Toulouse, Pediatric and Congenital Cardiology, Children's Hospital, Paul Sabatier University, Toulouse, France.
Radiol Case Rep
January 2025
Head of Department of Cardiology, Al Bassel Heart Institute, Damascus, Syria.
Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital deformity, and its association with truncus arteriosus (TA) has been infrequently described in medical literature. We report a case of a 3-year-old child presenting with failure to thrive and recurrent respiratory infections, who was diagnosed with truncus arteriosus type 1 and an anomalous left coronary artery originating from the pulmonary artery. The embryological basis of both TA and ALCAPA involves disruptions in the normal development of the aorticopulmonary septum and coronary arteries.
View Article and Find Full Text PDFCardiol Young
November 2024
Newcastle University, Newcastle Upon Tyne, UK.
We report two congenitally malformed hearts found at autopsy to have common arterial trunk and pulmonary atresia. Both exhibited usual atrial arrangement, along with concordant atrioventricular connections. In one case, the common arterial trunk arose predominantly from the right ventricle, while the other had a balanced commitment.
View Article and Find Full Text PDFJ Perinat Med
October 2024
Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, 12302 SUNY Upstate Medical University, Syracuse, NY, USA.
Objectives: Determine obstetrical and neonatal outcomes in neonates with major CHD delivered at a level IV neonatal intensive care units (NICU) center lacking onsite pediatric cardiac surgery.
Methods: A 10- year retrospective review of all neonates admitted to our level IV NICU, with CHD between January 1st, 2011 and December 31st, 2021. Births and NICU charts were cross queried with those from our perinatal center which include pediatric cardiology records.
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