van Hoorn Jeroen H L, Moonen Rob M J, Huysentruyt Clément J R, van Heurn L W Ernest, Offermans Jos P M, Mulder A L M Twan
Department of Pediatrics, University Hospital Maastricht, P.O. Box 5800, 6202 AZ, Maastricht, The Netherlands.
Eur J Pediatr. 2008 Jan;167(1):29-35. doi: 10.1007/s00431-007-0578-9. Epub 2007 Aug 4.
Two patients with incomplete pentalogy of Cantrell are described. The first was a girl with a large omphalocele with evisceration of the heart, liver and intestines with an intact sternum. Echocardiography showed profound intracardiac defects. The girl died 33 h after birth. The second patient was a female fetus with ectopia cordis (EC) without intracardiac anomalies; a large omphalocele with evisceration of the heart, stomach, spleen and liver; a hypoplastic sternum and rib cage; and a scoliosis. The pregnancy was terminated. A review of patients described in the literature is presented with the intention of finding prognostic factors for an optimal approach to patients with the pentalogy of Cantrell. In conclusion the prognosis seems to be poorer in patients with the complete form of pentalogy of Cantrell, EC, and patients with associated anomalies. Intracardial defects do not seem to be a prognostic factor.
本文描述了两名患有不完全性坎特雷尔五联症的患者。第一名是一名女孩,患有巨大脐膨出,心脏、肝脏和肠道外露,胸骨完整。超声心动图显示存在严重的心脏内缺陷。该女孩出生后33小时死亡。第二名患者是一名患有心脏异位(EC)且无心脏内异常的女性胎儿;伴有心脏、胃、脾和肝脏外露的巨大脐膨出;胸骨和胸廓发育不全;以及脊柱侧弯。该妊娠被终止。本文对文献中描述的患者进行了综述,旨在寻找针对坎特雷尔五联症患者的最佳治疗方法的预后因素。总之,坎特雷尔五联症完全型、心脏异位患者以及伴有相关异常的患者预后似乎更差。心脏内缺陷似乎不是一个预后因素。