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Acardius acephalus with spontaneous umbilical cord occlusion: Reporting a rare case

Twin reversed arterial perfusion syndrome is a rare obstetric condition that occurs in monochorionic twin pregnancies, resulting in coexistence of a normal “pump” twin and an acardiac twin. The acardiac twin is dependent upon the normal twin to provide circulation by means of vascular anastomosis, t...

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Autores principales: Arora, Suryansh, Lohiya, Nimisha, Singhal, Annu, Prasad, Akhila, Katyal, Aparna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8914117/
https://www.ncbi.nlm.nih.gov/pubmed/35282319
http://dx.doi.org/10.1016/j.radcr.2022.02.023
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author Arora, Suryansh
Lohiya, Nimisha
Singhal, Annu
Prasad, Akhila
Katyal, Aparna
author_facet Arora, Suryansh
Lohiya, Nimisha
Singhal, Annu
Prasad, Akhila
Katyal, Aparna
author_sort Arora, Suryansh
collection PubMed
description Twin reversed arterial perfusion syndrome is a rare obstetric condition that occurs in monochorionic twin pregnancies, resulting in coexistence of a normal “pump” twin and an acardiac twin. The acardiac twin is dependent upon the normal twin to provide circulation by means of vascular anastomosis, thereby putting the pump fetus at risk of high output cardiac failure. Overall only 50% of pump twins survive. Mortality for acardiac twin is 100%. We present a case of 26-year-old primigravida female presenting with 8 months of amenorrhea with unsure LMP. Ultrasonography followed by fetal MRI was carried out which revealed acardius acephalus twin with absence of blood flow in umbilical vessels. Pump twin had multicystic dysplastic left kidney with single umbilical artery. Following delivery, the pump twin survived well and the deformed fetus showed features of twin reversed arterial perfusion syndrome.
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spelling pubmed-89141172022-03-12 Acardius acephalus with spontaneous umbilical cord occlusion: Reporting a rare case Arora, Suryansh Lohiya, Nimisha Singhal, Annu Prasad, Akhila Katyal, Aparna Radiol Case Rep Case Report Twin reversed arterial perfusion syndrome is a rare obstetric condition that occurs in monochorionic twin pregnancies, resulting in coexistence of a normal “pump” twin and an acardiac twin. The acardiac twin is dependent upon the normal twin to provide circulation by means of vascular anastomosis, thereby putting the pump fetus at risk of high output cardiac failure. Overall only 50% of pump twins survive. Mortality for acardiac twin is 100%. We present a case of 26-year-old primigravida female presenting with 8 months of amenorrhea with unsure LMP. Ultrasonography followed by fetal MRI was carried out which revealed acardius acephalus twin with absence of blood flow in umbilical vessels. Pump twin had multicystic dysplastic left kidney with single umbilical artery. Following delivery, the pump twin survived well and the deformed fetus showed features of twin reversed arterial perfusion syndrome. Elsevier 2022-03-10 /pmc/articles/PMC8914117/ /pubmed/35282319 http://dx.doi.org/10.1016/j.radcr.2022.02.023 Text en © 2022 Published by Elsevier Inc. on behalf of University of Washington. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Arora, Suryansh
Lohiya, Nimisha
Singhal, Annu
Prasad, Akhila
Katyal, Aparna
Acardius acephalus with spontaneous umbilical cord occlusion: Reporting a rare case
title Acardius acephalus with spontaneous umbilical cord occlusion: Reporting a rare case
title_full Acardius acephalus with spontaneous umbilical cord occlusion: Reporting a rare case
title_fullStr Acardius acephalus with spontaneous umbilical cord occlusion: Reporting a rare case
title_full_unstemmed Acardius acephalus with spontaneous umbilical cord occlusion: Reporting a rare case
title_short Acardius acephalus with spontaneous umbilical cord occlusion: Reporting a rare case
title_sort acardius acephalus with spontaneous umbilical cord occlusion: reporting a rare case
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8914117/
https://www.ncbi.nlm.nih.gov/pubmed/35282319
http://dx.doi.org/10.1016/j.radcr.2022.02.023
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