TY - JOUR
T1 - First reported case of Pentalogy of Cantrell variant with good outcome in a 32 week gestational age monozygotic twin with twin-twin transfusion syndrome
AU - Srinivasakumar, Preethi
AU - Rama, Ganapathy
AU - Jesse, Nathan
AU - Howell, Rogers G.
AU - Brady, Joseph Lawrence
AU - Morales, Tania Tejera
AU - Maramreddy, Hima
AU - Hogan, Jenna
AU - Cosper, Graham H.
AU - Schmelzer, Thomas
AU - Bambini, Daniel A.
AU - Schulman, Andrew
AU - Kothadia, Jay
N1 - Funding Information:
Dr. Sharina Rajbhandari, Pediatrix Medical Group of North Carolina, MEDNAX Health Solutions Partner, Jessica Pierce, NP, Pediatric Surgical Associates, PA, Division of Maternal Fetal Medicine, Novant Health Presbyterian Medical Center, Division of Cardiology, Novant Health Presbyterian Medical Center, Novant Health Presbyterian Hospital Hemby NICU nursing and nurse practitioner team. Radhika Kothadia, MD, East Carolina University.
Publisher Copyright:
© 2019 The Authors
PY - 2019/12
Y1 - 2019/12
N2 - We report a case of a 32 week gestational age preterm monozygotic twin neonate with a rare variant of Pentalogy of Cantrell who presented with severe respiratory distress syndrome, possible pulmonary hypoplasia, large congenital diaphragmatic hernia, large omphalocele, and atrial septal defect. Pentalogy of Cantrell poses a unique challenge for both neonatologists and surgeons, as it has a high mortality and morbidity rate. Prognosis of newborns with Pentalogy of Cantrell depends upon severity of both cardiac and extracardiac defects, and other associated anomalies. This report describes an extremely rare variant of the Pentalogy of Cantrell spectrum in a patient with a co-existent twin – twin transfusion syndrome and transient hydrops fetalis in utero, who survived with favorable outcome.
AB - We report a case of a 32 week gestational age preterm monozygotic twin neonate with a rare variant of Pentalogy of Cantrell who presented with severe respiratory distress syndrome, possible pulmonary hypoplasia, large congenital diaphragmatic hernia, large omphalocele, and atrial septal defect. Pentalogy of Cantrell poses a unique challenge for both neonatologists and surgeons, as it has a high mortality and morbidity rate. Prognosis of newborns with Pentalogy of Cantrell depends upon severity of both cardiac and extracardiac defects, and other associated anomalies. This report describes an extremely rare variant of the Pentalogy of Cantrell spectrum in a patient with a co-existent twin – twin transfusion syndrome and transient hydrops fetalis in utero, who survived with favorable outcome.
KW - Giant omphalocele
KW - Monochornionic twin
KW - Pentalogy of cantrell
KW - Prematurity
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U2 - 10.1016/j.epsc.2019.101321
DO - 10.1016/j.epsc.2019.101321
M3 - Article
AN - SCOPUS:85073541600
SN - 2213-5766
VL - 51
JO - Journal of Pediatric Surgery Case Reports
JF - Journal of Pediatric Surgery Case Reports
M1 - 101321
ER -