Twin reversed arterial perfusion (TRAP) sequence in association with VACTERL association: a case report

<p>Abstract</p> <p>Introduction</p> <p>Twin reversed arterial perfusion (TRAP) sequence is a rare complication of multiple pregnancy caused by defects in early embryogenesis. The pump twin supplies the acardiac recipient twin with blood, and although the pump twin is us...

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Main Authors: Millard Katherine, Athwal Sharan, Lakhoo Kokila
Format: Article
Language:English
Published: BMC 2010-12-01
Series:Journal of Medical Case Reports
Online Access:http://www.jmedicalcasereports.com/content/4/1/411
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spelling doaj-ada65c285805415e8c01253e4f16ef9e2020-11-24T23:56:00ZengBMCJournal of Medical Case Reports1752-19472010-12-014141110.1186/1752-1947-4-411Twin reversed arterial perfusion (TRAP) sequence in association with VACTERL association: a case reportMillard KatherineAthwal SharanLakhoo Kokila<p>Abstract</p> <p>Introduction</p> <p>Twin reversed arterial perfusion (TRAP) sequence is a rare complication of multiple pregnancy caused by defects in early embryogenesis. The pump twin supplies the acardiac recipient twin with blood, and although the pump twin is usually structurally normal, congenital anomalies have sometimes been reported. We report a unique case of twin reversed arterial perfusion sequence with a prenatal diagnosis of VACTERL association in the surviving pump twin.</p> <p>Case presentation</p> <p>A 24-year-old Caucasian woman presented at 11 weeks' gestation with a monochorionic, monoamniotic twin pregnancy. A reversed arterial flow was noted on a Doppler imaging study coming from the larger, apparently normal twin to the smaller, grossly abnormal twin, and a diagnosis of twin reversed arterial perfusion sequence was made. Cardiac activity was undetectable in the recipient twin by 16 weeks' gestation. Further detailed assessment at 18 weeks' gestation revealed multiple congenital anomalies of the surviving pump twin, in keeping with a diagnosis of VACTERL association. A live infant girl was delivered at 39 weeks by elective cesarean section. She underwent extensive surgery with subsequent normal development at the age of two years.</p> <p>Conclusion</p> <p>The co-existence of two rare and complex conditions in this unique case raises interesting questions about the role of early defects in embryogenesis and their subsequent effects on fetal development. This case also highlights the importance of prenatal diagnosis of major congenital anomalies to the plan treatment, reduce morbidity and aid the survival of affected children.</p> http://www.jmedicalcasereports.com/content/4/1/411
collection DOAJ
language English
format Article
sources DOAJ
author Millard Katherine
Athwal Sharan
Lakhoo Kokila
spellingShingle Millard Katherine
Athwal Sharan
Lakhoo Kokila
Twin reversed arterial perfusion (TRAP) sequence in association with VACTERL association: a case report
Journal of Medical Case Reports
author_facet Millard Katherine
Athwal Sharan
Lakhoo Kokila
author_sort Millard Katherine
title Twin reversed arterial perfusion (TRAP) sequence in association with VACTERL association: a case report
title_short Twin reversed arterial perfusion (TRAP) sequence in association with VACTERL association: a case report
title_full Twin reversed arterial perfusion (TRAP) sequence in association with VACTERL association: a case report
title_fullStr Twin reversed arterial perfusion (TRAP) sequence in association with VACTERL association: a case report
title_full_unstemmed Twin reversed arterial perfusion (TRAP) sequence in association with VACTERL association: a case report
title_sort twin reversed arterial perfusion (trap) sequence in association with vacterl association: a case report
publisher BMC
series Journal of Medical Case Reports
issn 1752-1947
publishDate 2010-12-01
description <p>Abstract</p> <p>Introduction</p> <p>Twin reversed arterial perfusion (TRAP) sequence is a rare complication of multiple pregnancy caused by defects in early embryogenesis. The pump twin supplies the acardiac recipient twin with blood, and although the pump twin is usually structurally normal, congenital anomalies have sometimes been reported. We report a unique case of twin reversed arterial perfusion sequence with a prenatal diagnosis of VACTERL association in the surviving pump twin.</p> <p>Case presentation</p> <p>A 24-year-old Caucasian woman presented at 11 weeks' gestation with a monochorionic, monoamniotic twin pregnancy. A reversed arterial flow was noted on a Doppler imaging study coming from the larger, apparently normal twin to the smaller, grossly abnormal twin, and a diagnosis of twin reversed arterial perfusion sequence was made. Cardiac activity was undetectable in the recipient twin by 16 weeks' gestation. Further detailed assessment at 18 weeks' gestation revealed multiple congenital anomalies of the surviving pump twin, in keeping with a diagnosis of VACTERL association. A live infant girl was delivered at 39 weeks by elective cesarean section. She underwent extensive surgery with subsequent normal development at the age of two years.</p> <p>Conclusion</p> <p>The co-existence of two rare and complex conditions in this unique case raises interesting questions about the role of early defects in embryogenesis and their subsequent effects on fetal development. This case also highlights the importance of prenatal diagnosis of major congenital anomalies to the plan treatment, reduce morbidity and aid the survival of affected children.</p>
url http://www.jmedicalcasereports.com/content/4/1/411
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AT athwalsharan twinreversedarterialperfusiontrapsequenceinassociationwithvacterlassociationacasereport
AT lakhookokila twinreversedarterialperfusiontrapsequenceinassociationwithvacterlassociationacasereport
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