Results 31 to 40 of about 515 (147)
A Rare Case of Heterotaxy Syndrome Associated with Hepatolithiasis and Pre-duodenal Portal Vein [PDF]
Polysplenia syndrome is characterised by spectrum of abnormalities which are rarely diagnosed in adults as an incidental finding. The anomalies include multiple spleens, midline liver, gall bladder and biliary tract anomalies, short pancreas, agenesis ...
Varna Shetty +2 more
doaj +1 more source
Splenic torsion in the setting of polysplenia syndrome
Background: Polysplenia syndrome is a rare condition that occurs when polysplenia co-exists with various other congenital anomalies. Splenic torsion in the setting of polysplenia syndrome is extremely rare, having been documented only five times ...
Margaret Kennedy +2 more
doaj +1 more source
Pneumatosis intestinalis (PI) is a radiographic finding which refers to the presence of gas within the wall of any part of the gastrointestinal tract. While in some cases it is an incidental finding which usually represent its benign nonischemic etiology, it may indicate a catastrophic intra‐abdominal condition and distinctly characteristic of ischemic
Osama Shaheen +3 more
wiley +1 more source
Duodenal Atresia: Open versus MIS Repair—Analysis of Our Experience over the Last 12 Years
Objective. Duodenal atresia (DA) routinely has been corrected by laparotomy and duodenoduodenostomy with excellent long‐term results. We revisited the patients with DA treated in the last 12 years (2004–2016) comparing the open and the minimally invasive surgical (MIS) approach. Methods. We divided our cohort of patients into two groups.
Salvatore Fabio Chiarenza +7 more
wiley +1 more source
Pregnancy Complicated by Portal Hypertension Secondary to Biliary Atresia
Biliary atresia is a rare idiopathic neonatal cholestatic disease characterized by the destruction of both the intra‐ and extrahepatic biliary ducts. As the disease is progressive all cases will develop portal fibrosis, cirrhosis, and portal hypertension with the sequelae of varices, jaundice, and eventually liver failure requiring a transplant ...
O. E. O′Sullivan +7 more
wiley +1 more source
Biliary Atresia: 50 Years after the First Kasai
Biliary atresia is a rare neonatal disease of unknown etiology, where obstruction of the biliary tree causes severe cholestasis, leading to biliary cirrhosis and death in the first years of life, if the condition is left untreated. Biliary atresia is the most frequent surgical cause of cholestatic jaundice in neonates and should be evoked whenever this
Barbara E. Wildhaber +4 more
wiley +1 more source
Veine Porte Préduodénale: A Propos d′un Cas
Une veine porte préduodénale fut découverte a l′operation chez un enfant de huit ans qui resscntait des douleurs épigastriques post prandiales soulagées par vornisSernenrs depuis deux ans et qui a présenté deux épisodes de pancréatitc ayant néccssité l′hospitalisation dans la derniére année. L′anomalie de la vésicule biliaire a la cholécystographic, le
R. Cloutier, J. Laliberté
wiley +1 more source
Open Cholecystectomy for a Patient with Preduodenal Portal Vein
Yusuke Ohashi +2 more
exaly +3 more sources
The operations for congenital duodenal obstruction due to duodenal atresia with, annular pancreas still present a unique challenge. Of the operative techniques mentioned in the literature duodenoduodenostomy was the most frequently performed, however ...
Samuel Wabada +5 more
doaj +1 more source
Polysplenia syndrome in the adult patient. Case report with review of the literature
Aims: To report a case of polysplenia syndrome (PSS) in an adult patient. Background: The PSS is a form of situs ambiguos with multiple spleen, cardiac anomalies, abdominal heterotaxia, short pancreas, major venous system and bronquial malformations.
Juan José Plata-Muñoz +5 more
doaj +1 more source

