Bianca S, Bartoloni G, Auditore S, Reale A, Tetto C, Ingegnosi C, Pirruccello B, Ettore G
Centro di Consulenza Genetica e di Teratologia della Riproduzione, Catania, Italy.
Cardiology. 2006;105(1):37-40. doi: 10.1159/000088758. Epub 2005 Oct 7.
Ectopia cordis is a very rare congenital malformation, commonly associated with intracardiac anomalies. It is due to a defect in fusion of the anterior chest wall resulting in an extrathoracic location of the heart. We report prenatal 2-dimensional (2D) and 3D ultrasonography diagnosis and postnatal autoptic findings of an isolated ectopia cordis with tricuspid atresia. Ectopia cordis prenatal diagnosis is easily made with ultrasound by visualizing the heart outside the thoracic cavity. 3D ultrasonography may add more detailed visualization of the heart anomaly even if the 2D ultrasonography alone permits the prenatal diagnosis. Obstetrical management should include a careful search for associated anomalies, especially cardiac, and the assessment of fetal karyotype. As this is considered a sporadic anomaly, the recurrence risk is low and no genetic origin is known.
心脏异位是一种非常罕见的先天性畸形,通常与心内异常有关。它是由于前胸壁融合缺陷导致心脏位于胸腔外。我们报告了一例孤立性心脏异位合并三尖瓣闭锁的产前二维(2D)和三维超声诊断及产后尸检结果。通过超声观察胸腔外的心脏,很容易做出心脏异位的产前诊断。即使仅二维超声就能进行产前诊断,三维超声也可能会更详细地显示心脏异常。产科处理应包括仔细寻找相关异常,尤其是心脏异常,并评估胎儿核型。由于这被认为是一种散发性异常,复发风险低且病因不明。