Foregut duplication cyst associated with esophageal atresia and tracheoesophageal fistula: A case report and literature review

2013 ◽  
Vol 48 (5) ◽  
pp. e5-e7 ◽  
Author(s):  
J. Leslie Knod ◽  
Aaron P. Garrison ◽  
Jason S. Frischer ◽  
Belinda Dickie
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Esophageal Atresia ◽  
Tracheoesophageal Fistula ◽  
Duplication Cyst ◽  
Foregut Duplication Cyst

scholarly journals Small intestine duplication cyst with recurrent hematochezia: a case report and literature review

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Zhicheng Zhang ◽  
Xiaowei Huang ◽  
Qian Chen ◽  
Demin Li ◽  
Qi Zhou ◽  
...  
Keyword(s):  
Small Intestine ◽  
Case Report ◽  
Literature Review ◽  
Ct Scan ◽  
Duplication Cyst ◽  
Abdominal Ct ◽  
Case Presentation ◽  
Abdominal Ct Scan ◽  
Capsule Endoscopes

Abstract Background Small intestine duplication cysts (SIDCs) are rare congenital anatomical abnormalities of the digestive tract and a rare cause of hematochezia. Case presentation We describe an adult female presented with recurrent hematochezia. The routine gastric endoscope and colonic endoscope showed no positive findings. Abdominal CT scan indicated intussusception due to the "doughnut" sign, but the patient had no typical symptoms. Two subsequent capsule endoscopes revealed a protruding lesion with bleeding in the distal ileum. Surgical resection was performed and revealed a case of SIDC measuring 6 * 2 cm located inside the ileum cavity. The patient remained symptom-free throughout a 7-year follow-up period. Conclusion SIDCs located inside the enteric cavity can easily be misdiagnosed as intussusception by routine radiologic examinations.

scholarly journals Isolated Vaginal Agenesis Associated with Multiple Gastrointestinal Anomalies: A Case Report

2016 ◽  
Vol 5 (3) ◽  
pp. 32 ◽  
Author(s):  
Rossella Angotti ◽  
Francesco Molinaro ◽  
Anna Lavinia Bulotta ◽  
Francesco Ferrara ◽  
Marina Sica ◽  
...  
Keyword(s):  
Case Report ◽  
Esophageal Atresia ◽  
Anorectal Malformation ◽  
Tracheoesophageal Fistula ◽  
Associated Anomalies ◽  
Vaginal Agenesis ◽  
Long Gap ◽  
Unusual Association ◽  
Long Gap Esophageal Atresia

More than 50% of infants with esophageal atresia have associated anomalies. We present a case report of a 46XX neonate with long-gap esophageal atresia and tracheoesophageal fistula (EA/TEF), anorectal malformation, bowel duplication and vaginal agenesis. This is an unusual association of abnormalities which had not yet described in literature.

scholarly journals One Stage Reconstruction of Esophageal Atresia and Distal Tracheoesophageal Fistula in a 3250-gm Neonate: A Case Report

2015 ◽  
Vol 05 (02) ◽  
pp. 147-150
Author(s):  
Bijay Upadhyay ◽  
Xuedong Wu ◽  
Jun Li ◽  
Ning Wang ◽  
Shanshan Zhang ◽  
...  
Keyword(s):  
Case Report ◽  
Esophageal Atresia ◽  
Tracheoesophageal Fistula ◽  
One Stage ◽  
One Stage Reconstruction

scholarly journals Gastric Duplication Cyst Associated with Esophageal Atresia and Anorectal Malformations: A Rare Association

2018 ◽  
Vol 7 (3) ◽  
pp. 36
Author(s):  
Rajat Piplani ◽  
Deepak Bagga ◽  
Samir K Acharya
Keyword(s):  
Esophageal Atresia ◽  
Tracheoesophageal Fistula ◽  
Abdominal Distension ◽  
Anorectal Malformations ◽  
Duplication Cyst ◽  
Gastric Duplication ◽  
Gastric Duplication Cyst ◽  
Rare Association ◽  
Good Outcome ◽  
Post Operative Period

Esophageal atresia (EA) and tracheoesophageal fistula (TEF) and anorectal malformations (ARM) in a newborn usually present with frothing of saliva and massive abdominal distension rendering it difficult to diagnose associated intrabdominal pathologies. We report a large gastric duplication (GD) cyst in a 2-day-old neonate with EA and TEF. GD cyst was detected in the early post-operative period as the abdominal distension persisted after repair of EA and TEF. The baby underwent excision of GD cyst with good outcome thereafter.

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