scholarly journals Abdominal wall defect found at the first-trimester ultrasound scan

2020 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
Marília Freixo ◽  
Elisa Soares ◽  
Maria Coelho ◽  
Carla Marinho ◽  
AnaRita Pinto ◽  
...  
2020 ◽  
Vol 0 (0) ◽  
pp. 0
Author(s):  
Marilia Freixo ◽  
Elisa Soares ◽  
Maria Coelho ◽  
Carla Marinho ◽  
AnaRita Pinto ◽  
...  

2020 ◽  
Vol 48 (12) ◽  
pp. 030006052098021
Author(s):  
Yi Yang ◽  
Hong Wang ◽  
Zhenpeng Wang ◽  
Xuefeng Pan ◽  
Ying Chen

Body stalk anomaly is a rare abnormality characterized by an abdominal wall defect with evisceration of abdominal organs, severe kyphoscoliosis, and a very short or absent umbilical cord. Ectopia cordis (EC) is a rare, lethal anomaly characterized by complete or partial malpositioning of the heart outside of the thorax. A 28-year-old healthy primigravida was referred to our department to undergo a nuchal translucency thickness scan at 12 weeks’ gestation. The scan revealed typical features of body stalk anomaly and EC. Given the lethal condition of the fetus, the patient opted for termination of the pregnancy. Body stalk anomalies, especially those complicated by EC, are universally lethal for the affected fetus. Selective termination should be recommended to avoid possible complications that can arise during pregnancy. Additionally, the future parents should be informed that because the condition is not associated with chromosomal abnormalities, there is no increased risk of recurrence.


2021 ◽  
pp. 2105614
Author(s):  
Xiangyi Yin ◽  
Yuanping Hao ◽  
Yun Lu ◽  
Dongjie Zhang ◽  
Yaodong Zhao ◽  
...  

2007 ◽  
Vol 23 (2) ◽  
pp. 117-120
Author(s):  
Philippe Roth ◽  
Alain Martin ◽  
Fariz Bawab ◽  
Florence Fellmann ◽  
Didier Aubert ◽  
...  

NeoReviews ◽  
2005 ◽  
Vol 6 (3) ◽  
pp. e160-e163
Author(s):  
Valerie Chock

2018 ◽  
Vol 4 (2) ◽  
pp. 027010 ◽  
Author(s):  
Dmytro Zaworonkow ◽  
Mykola Chekan ◽  
Katarzyna Kusnierz ◽  
Andrzej Lekstan ◽  
Aniela Grajoszek ◽  
...  

2018 ◽  
Vol 2018 ◽  
pp. 1-4
Author(s):  
Jayan George ◽  
Michael Peirson ◽  
Samuel Birks ◽  
Paul Skinner

We describe the case of a 37-year-old gentleman with Crohn’s disease and a complex surgical history including a giant incisional hernia with no abdominal wall. He presented on a Sunday to the general surgical on-call with a four-day history of generalised abdominal pain, nausea, and decreased stoma output following colonoscopy. After CT imaging, he was diagnosed with a large colonic perforation. Initially, he was worked up for theatre but following early senior input, a conservative approach with antibiotics was adopted. The patient improved significantly and is currently awaiting plastic surgery input for the management of his abdominal wall defect.


2012 ◽  
Vol 2012 ◽  
pp. 1-3
Author(s):  
Mustapha El Kouache ◽  
S. Labib ◽  
A. El Madi ◽  
A. Babakhoya ◽  
S. Atmani ◽  
...  

Cantrell syndrome is a very rare congenital disease associating five features: a midline, upper abdominal wall disorder, lower sternal abnormality, anterior diaphragmatic defect, diaphragmatic pericardial abnormality, and congenital abnormalities of the heart. In this paper, we report a case of partial Cantrell's syndrome with left ventricular diverticulum, triatrial situs solitus, ventricular septal defect, dextrorotation of the heart, an anterior pericardial diaphragmatic defect, and a midline supraumbilical abdominal wall defect with umbilical hernia. The 5-month-old patient underwent a successful cardiac surgical procedure. A PTFE membrane was placed on the apex of the heart to facilitate reopening of the patient’s chest. Postoperative course was uneventful. The patient was discharged with good clinical condition and with a normal cardiac function.


Surgery ◽  
2019 ◽  
pp. 417-422
Author(s):  
Justin P. Wagner ◽  
Rivfka Shenoy ◽  
Steven L. Lee

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