Thoracoabdominal wall defect with complete ectopia cordis and gastroschisis: a case report and review of the literature.
نویسندگان
چکیده
Ventral wall defects are extremely rare anomalies that are likely caused by the failure of the ventral wall to close during week 4 of development. We report a case of severe thoracoabdominal wall defect including complete thoracic ectopia cordis and gastroschisis. This combination represents a novel constellation of findings in a single patient. This unique case further demonstrates an anatomically normal heart with age-appropriate development and an intact diaphragm. We review the literature of other reports and discussions of entities that share overlapping features with this case.
منابع مشابه
Partial Ectopia Cordis: A Case Report
Background: One-third of all major congenital anomalies are Congenital heart disease (CHD) and Reported CHD prevalence increased over time and in Asian countries is more than western countries. Ectopia cordis (EC) is a rare congenital anomaly with an estimated incidence of 1:100 000 live births in developed countries. EC is characterized by abnormal heart placement outside the thorax, mostly on...
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Ectopia cordis is a rare congenital defect in which the heart is displaced partially or completely, out of the chest. We present a case of term male neonate, delivered by elective caesarean section, asphyxiated and transferred to neonatal intensive unit at one hour of age. The baby had thoracic ectopia cordis and gastroschisis. The baby was unstable, cyanosed, required vasopressors and ventilat...
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Introduction: Ectopia cordis is a rare congenital defect and a true neonatal surgical emergency, with an occurrence of 5.5 to 7.9 cases per million live births [1]. This impressive malformation develops due to failure of maturation of the midline mesodermal components of the chest and abdomen [2]. The disorder is classified into five anatomical types including cervical, cervicothoracic, thoraci...
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ورودعنوان ژورنال:
- Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
دوره 16 5 شماره
صفحات -
تاریخ انتشار 2013