Results 11 to 20 of about 176,743 (268)

Congenital Portosystemic Shunt: Our Experience [PDF]

open access: yesCase Reports in Pediatrics, 2015
Introduction. Congenital portosystemic venous malformations are rare abnormalities in which the portal blood drains into a systemic vein and which are characterized by extreme clinical variability.Case Presentations. The authors present two case reports of a congenital extrahepatic portosystemic shunt (Type II).
Timpanaro, Tiziana   +7 more
openaire   +4 more sources

A pediatric case of portosystemic shunt presenting hypoxemia with brain abscess in an emergency department [PDF]

open access: yesPediatric Emergency Medicine Journal, 2023
Portosystemic shunt is a rare congenital vascular anomaly. The shunt is hard to clinically suspect because its symptoms develop insidiously and affect various systems at different time points.
Seong Taek Hwang, Jun Sung Park
doaj   +1 more source

First Report of Fulminant Budd-Chiari Syndrome Treated by Direct Intrahepatic Portocaval Shunt in Vietnam

open access: yesCase Reports in Gastroenterology, 2021
Budd-Chiari syndrome (BCS) is a rare disorder caused by hepatic venous outflow obstruction that can lead to acute liver failure proposing liver transplantation or transjugular intrahepatic portosystemic shunt.
Thai Van Nguyen   +3 more
doaj   +1 more source

Caution for living donor liver transplantation with congenital portosystemic shunt: a case report

open access: yesSurgical Case Reports, 2022
Background Congenital portosystemic shunt is an infrequent abnormal connection between the portal vascular system and the systemic circulation. Portosystemic shunts are common findings in patients with cirrhosis, causing gastroesophageal varices, hepatic
Yoshihiro Nagao   +13 more
doaj   +1 more source

Combination of Model for End‐Stage Liver Disease and Lactate Predicts Death in Patients Treated With Salvage Transjugular Intrahepatic Portosystemic Shunt for Refractory Variceal Bleeding

open access: yesHepatology, 2021
Data about the prognosis of salvage transjugular intrahepatic portosystemic shunt (TIPS) using covered stents for refractory variceal bleeding caused by portal hypertension are scarce.
A. Walter   +21 more
semanticscholar   +1 more source

Laparoscopic portosystemic shunt attenuation in two cats

open access: yesJournal of Feline Medicine and Surgery Open Reports, 2022
Case series summary Gradual attenuation of an extrahepatic portosystemic shunt using cellophane banding was achieved with a laparoscopic technique in two cats.
Francesca Izzo   +3 more
doaj   +1 more source

Progress of pulmonary hypertension and high manganese levels through congenital portosystemic shunt closure

open access: yesClinical Case Reports, 2022
A 6‐year‐old girl with congenital portosystemic shunt presented with abnormal manganese levels and improving pulmonary hypertension even 1 year after shunt vascular ligation. As the progress after portal vein blood flow recovery varies among individuals,
Toshihiko Kakiuchi   +4 more
doaj   +1 more source

Transjugular intrahepatic portosystemic shunt in cirrhosis: An exhaustive critical update

open access: yesWorld Journal of Gastroenterology, 2020
More than five decades after it was originally conceptualized as rescue therapy for patients with intractable variceal bleeding, the transjugular intrahepatic portosystemic shunt (TIPS) procedure continues to remain a focus of intense clinical and ...
S. Rajesh   +7 more
semanticscholar   +1 more source

Spontaneous Resolution of Congenital Intrahepatic Portosystemic Shunt. [PDF]

open access: yesActa Med Litu
Congenital portosystemic shunts (CPSS) are a rare type of congenital abnormality. It results from abnormal embryonic development by the fourth week of fetal life.
Tripathy T   +5 more
europepmc   +2 more sources

Etiology and treatment of recurrent consciousness disorders following hepatobiliary surgery: Insights from a portosystemic shunt case study. [PDF]

open access: yesJ Int Med Res
Intrahepatic portosystemic venous shunt is a rare vascular anomaly that can occur congenitally or iatrogenically, leading to hyperammonemia and neurological complications such as hepatic encephalopathy.
Jin Y, Wang Y, Chen W, Wang H.
europepmc   +2 more sources

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