scholarly journals Prenatal Detection and Postnatal Verification of Unusual Intracardiac Total Anomolous Pulmonary Venous Connection (Tapvc) in Complex Heart Defect with Dextrocardia - Case Report

2018 ◽  
Vol 8 (1) ◽  
pp. 59-63
Author(s):  
Aneta Krasoń ◽  
Joanna Płużańska ◽  
Maciej Łukaszewski ◽  
Jadwiga Moll ◽  
Maria Respondek-Liberska
Keyword(s):  
Cardiac Surgery ◽  
Case Report ◽  
Prenatal Diagnosis ◽  
Fetal Echocardiography ◽  
Heart Murmur ◽  
Prenatal Detection ◽  
Heart Defect

Abstract Prenatal diagnosis of total anomolous pulmonary venous connection (intracardiac) was diagnosed in fetus with dextrocardia and complex heart defect, which allowed fetal echocardiography monitoring, planning the time and place for delivery as well as early cardiac surgery. The differences between prenatal and postnatal evaluations were underlined. Despite life treathening condition neonate was asymptomatic without any heart murmur for the first 3 days after delivery.

Emerging trends in the prenatal diagnosis of complex CHD and its influence on infant mortality in this cohort

2018 ◽  
Vol 29 (3) ◽  
pp. 270-276 ◽  
Author(s):  
Sudheer R. Gorla ◽  
Abhishek Chakraborty ◽  
Ashish Garg ◽  
Rubee A. Gugol ◽  
Richard E. Kardon ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Infant Mortality ◽  
Chart Review ◽  
Fetal Echocardiography ◽  
Tertiary Care ◽  
Retrospective Chart Review ◽  
Tertiary Care Centre ◽  
Prenatal Detection ◽  
Emerging Trends ◽  
Conotruncal Anomalies

AbstractBackgroundFetal echocardiography is the main modality of prenatal diagnosis of CHD. This study was done to describe the trends and benefits associated with prenatal diagnosis of complex CHD at a tertiary care centre.MethodsRetrospective chart review of patients with complex CHD over an 18-year period was performed. Rates of prenatal detection along with early and late infant mortality outcomes were studied.ResultsOf 381 complex CHD patients born during the study period, 68.8% were diagnosed prenatally. Prenatal detection rate increased during the study period from low-50s in the first quarter to mid-80s in the last quarter (p=0.001). Rate of detection of conotruncal anomalies increased over the study period. No infant mortality benefit was noted with prenatal detection.ConclusionsImproved obstetrical screening indications and techniques have contributed to higher proportions of prenatal diagnosis of complex CHD. However, prenatal diagnosis did not confer survival benefits in infancy in our study.

scholarly journals Isolated Double Aortic Arch (Daa) – Prenatal Detection with Postnatal Follow-Up, Case Report and Literature Review

2018 ◽  
Vol 8 (1) ◽  
pp. 64-70
Author(s):  
Julia Murlewska ◽  
Agnieszka Żalińska ◽  
Danuta Roik ◽  
Bożena Werner ◽  
Maria Respondek-Liberska
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Literature Review ◽  
Aortic Arch ◽  
Clinical Symptoms ◽  
Double Aortic Arch ◽  
Computer Reconstruction ◽  
Prenatal Detection ◽  
Angio Ct

Abstract This case report presents a prenatal diagnosis with postnatal confirmation (by angio CT and computer reconstruction) of an isolated double aortic arch, with no blood disturbances and with no clinical symptoms after birth. Literature review was focusing on the possible symptoms in the future. Prenatal findings should be forwarded to neonatologist and pediatrician despite clinical silence.

Prenatal diagnosis of Marfan syndrome by fetal echocardiography: A case report and review of cardiovascular manifestations

2019 ◽  
Vol 37 (2) ◽  
pp. 359-362
Author(s):  
Xin Wang ◽  
Lin Sun ◽  
Xiao‐Wei Liu ◽  
Jian‐Feng Shang ◽  
Yi‐Hua He
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Marfan Syndrome ◽  
Fetal Echocardiography

Prenatal diagnosis of Berry syndrome by fetal echocardiography: a case report

2016 ◽  
Vol 33 (10) ◽  
pp. 1611-1613 ◽  
Author(s):  
Shui-Hua Yang ◽  
Xiao-Xian Tian ◽  
Yuan-Yuan Li ◽  
Zuo-Jian Yang
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Fetal Echocardiography ◽  
Berry Syndrome

Case report of Erdheim-Chester disease in a female cardiac surgery patient

2011 ◽  
Vol 59 (S 01) ◽  
Author(s):  
HR Mahoozi ◽  
A Zittermann ◽  
K Hakim-Meibodi ◽  
J Gummert ◽  
N Mirow
Keyword(s):  
Cardiac Surgery ◽  
Case Report ◽  
Cardiac Surgery Patient ◽  
Erdheim Chester Disease ◽  
Surgery Patient ◽  
Erdheim Chester ◽  
Chester Disease

Prenatal diagnosis of an epignathus associated with a 49, XXXXY karyotype – a case report

2007 ◽  
Vol 28 (S 1) ◽  
Author(s):  
I Staboulidou ◽  
K Miller ◽  
G Göhring ◽  
P Hillemanns ◽  
M Wüstemann
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis

Early fetal echocardiography: a new challenge in prenatal diagnosis

2002 ◽  
Vol 2 (4) ◽  
pp. 251-260
Author(s):  
J. M. Martínez ◽  
O. Gómez ◽  
M. del Río ◽  
B. Puerto ◽  
A. Borrell ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Fetal Echocardiography

Mature teratoma splitting the brainstem in a newborn: case report

2019 ◽  
Vol 24 (4) ◽  
pp. 371-375
Author(s):  
Li-tal Pratt ◽  
Shelly I. Shiran ◽  
Ronit Precel ◽  
Liat Ben-Sira ◽  
Gustavo Malinger ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Posterior Fossa ◽  
Mature Teratoma

Mature teratomas (MTs) of the posterior fossa are extremely rare. The authors present a case of a prenatal diagnosis of an MT splitting the brainstem. Representative images as well as the clinical and surgical course are presented. Literature regarding “split brainstem” and MT of the posterior fossa is discussed.

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