scholarly journals BILE DUCT ANOMALIES ASSOCIATED WITH DUODENAL ATRESIA; PARADOXICAL PRESENCE OF SMALL BOWEL GAS

1972 ◽  
Vol 116 (3) ◽  
pp. 577-583 ◽  
Author(s):  
E. KASSNER GEORGE ◽  
ALBERT L. SUTTON ◽  
THEODORE J. DE GROOT
1985 ◽  
Vol 20 (2) ◽  
pp. 167-168 ◽  
Author(s):  
G. Patti ◽  
G. Marrocco ◽  
G. Mazzoni ◽  
A. Catarci

2020 ◽  
Vol 225 ◽  
pp. 275
Author(s):  
Cornelia Griggs ◽  
Carrie Ruzal-Shapiro ◽  
Erica Fallon

2019 ◽  
Vol 2019 ◽  
pp. 1-6 ◽  
Author(s):  
Ju Hao ◽  
Yao Zhang ◽  
Li Tianyu ◽  
Shi Bo ◽  
Feng Shu ◽  
...  

Purpose. To assess the diagnostic value of ultrasonography (US) for congenital small bowel atresia (SBA) in neonates and their sonographic characteristics. Methods. A retrospective analysis was performed of 20 neonates who were confirmed with SBA by operation from March 2014 to January 2019. All the neonates have been scanned by US before surgery, and no one underwent barium enema or upper gastrointestinal imaging prior to US. Preoperation ultrasound characteristics about intestinal morphology and intestinal contents were collected, further to summarize the typical ultrasonic features of SBA. Results. Five cases were duodenal atresia, and 15 cases were jejuno-ileal atresia. Distended proximal intestines, liquid with tiny points in it, can be found in 20 neonates. The small intestine without any gas can be found in 20 neonates. Microcolon, no gas and other contents in it, can be found in 16 cases. Conclusions. The typical ultrasonic features of SBA include dilation in proximal intestines, small intestines, and microcolon. US is a promising modality in the clinical diagnosis of SBA.


1992 ◽  
Vol 22 (2) ◽  
pp. 118-119
Author(s):  
J. T. Wald ◽  
L. C. Foley ◽  
A. Mezoff ◽  
M. Bourque

HPB Surgery ◽  
2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
Alexandros K. Charalabopoulos ◽  
Sylvia P. Krivan ◽  
Nikolas A. Machairas ◽  
P. Evangelos Misiakos ◽  
Anastasios N. Machairas

Peutz-Jeghers syndrome is a rare autosomal dominant inherited disease characterized by a special type of hamartomatous gastrointestinal polyps combined with mucocutaneous melanin pigmentations. Patients with the syndrome have a high risk of developing neoplasia, with colon, small bowel, and stomach being the most common gastrointestinal sites. Herein, we present the occurrence of a rare tumor in patients with Peutz-Jeghers syndrome; a cholangiocarcinoma of the endopancreatic bile duct. A minireview is also presented. It can be concluded that cholangiocarcinoma remains a possible diagnosis in PJS patients, as in others that present with biliary obstruction. PJS patients may be at higher risk than others in view of their propensity for malignancy.


Author(s):  
Mike Stanton

This chapter covers the common congenital abnormalities. This includes detailed discussion of the gut development. Conditions covered include gastroschisis, exomphalos, malrotation, duodenal atresia, small bowel obstruction, distal intestinal obstruction, meconium ileus, Hirschsprung disease, and anorectal malformation.


2006 ◽  
Vol 22 (9) ◽  
pp. 709-718 ◽  
Author(s):  
Hayrettin Ozturk ◽  
Halil Eken ◽  
Hulya Ozturk ◽  
Huseyin Buyukbayram

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