A gastroschisis-like abdominal wall defect in the leff hypochondrium. Case report and literature review

1998 ◽  
Vol 33 (9) ◽  
pp. 1452
Author(s):  
Thomas A. Angerpointner
1998 ◽  
Vol 8 (01) ◽  
pp. 52-54 ◽  
Author(s):  
M. Melikoğlu ◽  
G. Karagüzel ◽  
M. Oğüş ◽  
A. Aslan ◽  
M. Inan

2014 ◽  
Vol 3 (1) ◽  
pp. 19-23 ◽  
Author(s):  
Dalibor Divkovic ◽  
Slavica Kvolik ◽  
Mirna Sipl ◽  
Krunoslav Sego ◽  
Silvija Puseljic ◽  
...  

Microsurgery ◽  
2018 ◽  
Vol 39 (2) ◽  
pp. 174-177 ◽  
Author(s):  
Annika Senghaas ◽  
Thomas Kremer ◽  
Volker J. Schmidt ◽  
Leila Harhaus ◽  
Christoph Hirche ◽  
...  

Microsurgery ◽  
2017 ◽  
Vol 39 (1) ◽  
pp. 85-90 ◽  
Author(s):  
Dong Yeon Kim ◽  
Junho Lee ◽  
Jeong Tae Kim ◽  
Hye Kyung Chang ◽  
Suk-Ho Moon

2019 ◽  
Vol 6 (38) ◽  
pp. 2603-2605
Author(s):  
Ritu Saloi ◽  
Roonmoni Deka ◽  
Santanu Kumar Sarma

2019 ◽  
Vol XXIV (143) ◽  
pp. 54-58
Author(s):  
Sérgio Diego P. Costa ◽  
Durval Baraúna Junior ◽  
Jamilly N. Ramos Costa ◽  
Cássia Regina Oliveira Santos ◽  
Pâmela Raiely Pinheiro Moreira ◽  
...  

Hypospadia and omphalocele are rare congenital defects reported in various breeds, including the Doberman Pinscher, English Bulldog, French Bulldog, Basenji, and Dalmatian. Hypospadia is characterized by a defect in the fusion of the penile foreskin associated with persistent opening of the ventral urethral sulcus. Omphalocele is an abdominal wall defect, most common at the umbilical site, that may lead to evisceration of abdominal organs. Some dog breeds are suspected to have an hereditary predisposition to these conditions, but the etiology is still poorly understood, and believed to be multifactorial. We report a case of omphalocele and hypospadia in a French Bulldog neonate on which euthanasia was performed.


2020 ◽  
Vol 2020 ◽  
pp. 1-6
Author(s):  
Elise Abi Rached ◽  
N. Sananes ◽  
I. Kauffmann-Chevalier ◽  
F. Becmeur

Vanishing gastroschisis (VG) is a severe complication of gastroschisis with a high mortality rate. We report here a case of VG with a favorable outcome after a 3-year follow-up. A 26-year-old primigravida woman was referred to Strasbourg University Hospital because her fetus was diagnosed with an isolated gastroschisis at 13-week gestation. The ultrasound evolution was marked by a progressive closure of the abdominal wall defect from 19-week gestation and the appearance of dilated intra-abdominal loops. The child was born with a closed abdominal wall except a small remnant at the level of the former gastroschisis orifice. Explorative laparotomy revealed extensive midgut atresia with only 50 cm of remaining midgut. A jejunocolic anastomosis was performed. The child is now 3 years old and has a favorable outcome with only 2 nights a week of parenteral nutrition. A total of 39 cases of VG type D from Perrone et al. classification are described in the literature from 1991 to 2019, among which 19 (48.7%) are alive at the time of publication but only 4 cases are described with a long-term follow-up of 3 years or more. This is the fifth case described with a favorable evolution after 3-year follow-up.


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