Umbilical Cord Ulceration after Prenatal Diagnosis of Duodenal Atresia with Interstitial Deletion of Chromosome 13q: A Case Report

2008 ◽  
Vol 24 (2) ◽  
pp. 115-118 ◽  
Author(s):  
Hidehiko Miyake ◽  
Akihito Yamamoto ◽  
Takashi Yamada ◽  
Kaoru Okazaki ◽  
Kiyoko Morita ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Umbilical Cord ◽  
Duodenal Atresia ◽  
Interstitial Deletion ◽  
Chromosome 13Q

Sudden Fetal Death Associated with Both Duodenal Atresia and Umbilical Cord Ulcer: A Case Report and Review

2006 ◽  
Vol 23 (3) ◽  
pp. 183-188 ◽  
Author(s):  
Ai Anami ◽  
Seiichi Morokuma ◽  
Kiyomi Tsukimori ◽  
Haruhiko Kondo ◽  
Masahiro Nozaki ◽  
...  
Keyword(s):  
Case Report ◽  
Umbilical Cord ◽  
Fetal Death ◽  
Duodenal Atresia

scholarly journals PARTIAL CONGENITAL BOWEL OBSTRUCTION BY DUODENAL ATRESIA WINDSOCKS TYPE: CASE REPORT

2016 ◽  
Vol 7 (1) ◽  
Author(s):  
M. Molinaro ◽  
F. Mariscoli ◽  
M. Sica ◽  
E. Bindi ◽  
R. Angotti ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Surgical Treatment ◽  
Bowel Obstruction ◽  
Fetal Mri ◽  
Rare Condition ◽  
Duodenal Atresia ◽  
Prenatal Ultrasound ◽  
Double Bubble ◽  
Degree Of Certainty

<strong>Introduction</strong> Duodenal atresia Windsocks type is a rare condition of congenital bowel obstruction. Thanks to recent technological advancements of prenatal diagnosis it is possible to make a diagnosis of duodenal atresia with high degree of certainty through the radiological sign of “double bubble”, but up to date it is not yet possible to identify the type of duodenal atresia. We report the case of a patient with prenatal diagnosis of “double bubble”. The patient had no other concomitant malformations. <br /><strong>Case Report</strong> The patient came to our attention after prenatal ultrasound that showed a picture of double bubble. At the 27th week of gestation we performed fetal MRI that confirmed the US pattern of double bubble but it did not identify with certainty the type of duodenal atresia. At birth the patient underwent GI rx examination that showed a picture of partial duodenal obstruction compatible with the Windsocks type. On the following day, we performed endoscopy which showed the presence of duodenal membrane, so the patient underwent surgical treatment with a longitudinal duodenal incision in order to treat the wind-sock membrane. After one month a further Upper-GI rx examination showed a regular transit of the contrast. Four months after the first operation the patient underwent new surgical treatment for bowel obstruction by adhesions. The operation was successful and the patient had a complete recover.<br /><strong>Conclusions</strong> Patients with prenatal diagnosis of “double bubble” require a multidisciplinary approach for proper clinical management. Unfortunately it is not currently possible to identify with certainty by prenatal ultrasound the type of duodenal atresia, but in case of incomplete bowel occlusion , the possibility of an atresia Windsocks type should always be considered, especially for setting the right surgical approach.

scholarly journals VP11.22: Prenatal diagnosis of duodenal atresia: a case report

2021 ◽  
Vol 58 (S1) ◽  
pp. 142-143
Author(s):  
V.S. Arruarana ◽  
T. Anderson ◽  
O. Oseji ◽  
R. Johns ◽  
I. Benjamin ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Duodenal Atresia

Prenatal diagnosis of large subamniotic cyst compressing the umbilical cord on umbilicoplacental junction : A case report

2010 ◽  
Vol 53 (2) ◽  
pp. 169
Author(s):  
Ji Yeon Lee ◽  
Seung ho Shin ◽  
Sung hoon Na ◽  
Hyang Ah Lee ◽  
Dong Heon Lee ◽  
...  
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Umbilical Cord

Prenatal diagnosis of an epignathus associated with a 49, XXXXY karyotype – a case report

2007 ◽  
Vol 28 (S 1) ◽  
Author(s):  
I Staboulidou ◽  
K Miller ◽  
G Göhring ◽  
P Hillemanns ◽  
M Wüstemann
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis
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