Late prenatal diagnosis of complete pentalogy of Cantrell.

IF 0.5 Q4 OBSTETRICS & GYNECOLOGY
Maria Elisa Martini Albrecht, Roberto Sevillano Filho, Edward Araujo Júnior
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引用次数: 0

Abstract

Cantrell's pentalogy is a rare syndrome associated with a midline embryological defect involving a series of malformations: anomalies of the lower sternum, anterior diaphragm, heart, and anterior abdominal wall. It can be classified as complete, probable or partial, but the most important thing is to describe and understand the anomalies involved. We describe a case of a late diagnosis of Cantrell's pentalogy at 35 weeks and 5 days of pregnancy in a woman from the interior of Pará state, an Amazon Brazilian region. Fetal echocardiography confirmed the diagnosis of Cantrell's pentalogy with tetralogy of Fallot and ultrasound examination showing a bilateral clubfoot. Cesarean section was performed at 36 weeks because of pre-eclampsia superimposed on chronic arterial hypertension with signs of severity. The male newborn was delivered weighting 2,320 grams. Postnatal echocardiography confirmed the diagnosis of Cantrell's pentalogy and karyotype was normal (46, XY). Infant was discharged at 47 days of age with good weight gain, artificial breastfeeding, and outpatient follow-up by the cardiology and cardiac surgery specialists.

完全五联症的产前晚期诊断。
Cantrell's pentalogy是一种罕见的综合征,与中线胚胎学缺陷有关,包括一系列畸形:胸骨下段、前膈、心脏和前腹壁的异常。它可以分为完全、可能或部分,但最重要的是描述和理解所涉及的异常。我们描述了一个病例晚期诊断坎特雷尔五联症在35周和5天的怀孕在一个妇女从帕尔州内部,亚马逊巴西地区。胎儿超声心动图证实了Cantrell五联症和法洛四联症的诊断,超声检查显示双侧畸形足。由于先兆子痫叠加慢性动脉高血压的严重迹象,剖宫产于36周。男婴出生时重2320克。产后超声心动图证实Cantrell的五联症诊断和核型正常(46,XY)。婴儿在47天大时出院,体重增加良好,人工母乳喂养,由心脏病学和心脏外科专家门诊随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ceska Gynekologie-Czech Gynaecology
Ceska Gynekologie-Czech Gynaecology OBSTETRICS & GYNECOLOGY-
CiteScore
0.60
自引率
25.00%
发文量
57
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