Cargando…

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

INTRODUCTION: 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 so...

Descripción completa

Detalles Bibliográficos
Autores principales: Athwal, Sharan, Millard, Katherine, Lakhoo, Kokila
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022672/
https://www.ncbi.nlm.nih.gov/pubmed/21176185
http://dx.doi.org/10.1186/1752-1947-4-411
_version_ 1782196547851649024
author Athwal, Sharan
Millard, Katherine
Lakhoo, Kokila
author_facet Athwal, Sharan
Millard, Katherine
Lakhoo, Kokila
author_sort Athwal, Sharan
collection PubMed
description INTRODUCTION: 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. CASE PRESENTATION: 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. CONCLUSION: 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.
format Text
id pubmed-3022672
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-30226722011-01-19 Twin reversed arterial perfusion (TRAP) sequence in association with VACTERL association: a case report Athwal, Sharan Millard, Katherine Lakhoo, Kokila J Med Case Reports Case Report INTRODUCTION: 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. CASE PRESENTATION: 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. CONCLUSION: 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. BioMed Central 2010-12-22 /pmc/articles/PMC3022672/ /pubmed/21176185 http://dx.doi.org/10.1186/1752-1947-4-411 Text en Copyright ©2010 Athwal et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Athwal, Sharan
Millard, Katherine
Lakhoo, Kokila
Twin reversed arterial perfusion (TRAP) sequence in association with VACTERL association: a case report
title 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_short 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
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3022672/
https://www.ncbi.nlm.nih.gov/pubmed/21176185
http://dx.doi.org/10.1186/1752-1947-4-411
work_keys_str_mv AT athwalsharan twinreversedarterialperfusiontrapsequenceinassociationwithvacterlassociationacasereport
AT millardkatherine twinreversedarterialperfusiontrapsequenceinassociationwithvacterlassociationacasereport
AT lakhookokila twinreversedarterialperfusiontrapsequenceinassociationwithvacterlassociationacasereport