Schiavone Marcella, Pizzol Damiano, Colangelo Anna Claudia, Antunes Mario
Department of Emergency and Organ Transplantation-Section of Thoracic Surgery, University of Bari, Bari, Italy.
Italian Agency for Development Cooperation, Khartoum, Sudan.
J Surg Case Rep. 2020 Jun 1;2020(5):rjaa100. doi: 10.1093/jscr/rjaa100. eCollection 2020 May.
Cantrell syndrome (CS) is defined as congenital combination of five anomalies: defects at the lower part of the sternum, anterior diaphragm, midline supraumbilical abdominal wall, diaphragmatic pericardium and ectopia cordis. Antenatal screening should be performed to make an accurate prenatal diagnosis. The prognosis is usually poor with a high mortality early in life. The gold standard management is surgery but its prognosis remains poor. In many low-income settings prenatal examinations and surgery treatment are not possible. In the present case, we report a not surgery managed baby affected by CS, with good clinical conditions after 5 months.
坎特雷尔综合征(CS)被定义为五种异常的先天性组合:胸骨下部缺陷、前膈、脐上中线腹壁、膈心包和心脏异位。应进行产前筛查以做出准确的产前诊断。其预后通常较差,在生命早期死亡率很高。金标准治疗方法是手术,但预后仍然不佳。在许多低收入地区,无法进行产前检查和手术治疗。在本病例中,我们报告了一名未接受手术治疗的CS患儿,5个月后临床状况良好。