Results 21 to 30 of about 1,713 (227)

Previously undescribed anomalies of hepatic artery and portal venous anatomy in a case of extrahepatic biliary atresia and its implications

open access: yesJournal of Indian Association of Pediatric Surgeons, 2019
A search on PubMed and Web of Science revealed scarcity of the literature on anomalies of hepatic artery or portal vein and the presence of arterioportal fistula in biliary atresia; although, it has long-lasting implications for both the patient and the ...
Prabudh Goel   +3 more
doaj   +1 more source

The Value of Hepatic Scintigraphy in the Diagnosis of Biliary Atresia

open access: yesFrontiers in Pediatrics, 2022
IntroductionBiliary Atresia (BA) requires prompt diagnosis and surgical intervention to optimize its outcome. The aim of this study was to evaluate the accuracy of EHIDA in distinguishing between BA and other causes of cholestatic jaundice.MethodsThis ...
Wing Ki Chan   +2 more
doaj   +1 more source

Inflammation, Active Fibroplasia, and End-stage Fibrosis in 172 Biliary Atresia Remnants Correlate Poorly With Age at Kasai Portoenterostomy, Visceral Heterotaxy, and Outcome [PDF]

open access: yes, 2018
Published histologic studies of the hilar plate or entire biliary remnant at the time of Kasai portoenterostomy (KHPE) have not provided deep insight into the pathogenesis of biliary atresia, relation to age at surgery, prognosis or the basis for ...
Arva   +32 more
core   +1 more source

Biliary Lipid Excretion After Hepatic Portoenterostomy

open access: yesAnnals of Surgery, 1976
Since 1974, 16 consecutive infants with biliary atresia have been treated by hepatic portoenterostomy employing an exteriorized Roux-en-Y intestinal segment (Miluliez). Simultaneous, sequential analyses of bile pigments and lipids in serum and biliary drainage were performed.
J R, Lilly, N B, Javitt
openaire   +3 more sources

Probable posttransplant lymphoproliferative disorder after pediatric living donor liver transplantation: Is a biopsy still needed?

open access: yesClinical Case Reports, Volume 10, Issue 11, November 2022., 2022
We had five cases of pediatric probable posttransplant lymphoproliferative disorder after liver transplantation. If the patient's symptoms are too mild, excisional biopsy is too difficult to perform, or the patient is too sick to undergo invasive procedures, initiating preemptive treatment without a histological diagnosis could be the treatment option.
Muneyuki Matsumura   +10 more
wiley   +1 more source

Laparoscopy in liver transplantation: The future has arrived [PDF]

open access: yes, 2012
In the last two decades, laparoscopy has revolutionized the field of surgery. Many procedures previously performed with an open access are now routinely carried out with the laparoscopic approach.
Berloco, Pasquale Bartolomeo   +9 more
core   +2 more sources

Liver transplantation before 1 year of age [PDF]

open access: yes, 1987
Since 1981, 20 infants younger than 1 year of age received 26 orthotopic liver transplants. Immunosuppression was with cyclosporine and corticosteroids. Thirteen (65%) of the reciplents were discharged from the hospital.
Ascher   +18 more
core   +1 more source

‘Triangular Cord’ Sign in Biliary Atresia

open access: yes대한영상의학회지, 2022
Biliary atresia is an unknown etiology of extrahepatic bile duct obstruction with a ‘fibrous ductal remnant,’ which represents the obliterated ductal remnant in the porta hepatis.
Hee Jung Lee, Mu Sook Lee, Jin Young Kim
doaj   +1 more source

Balloon-occluded retrograde transvenous obliteration successfully performed for a large gastric varix in combination with temporary occlusion of the splenic artery in a child

open access: yesActa Radiologica Open, 2015
We encountered a 10-year-old boy with a gastric varix that occurred after long-term treatment by Kasai’s hepatic portoenterostomy for biliary atresia for which balloon-occluded retrograde transvenous obliteration (B-RTO) was performed.
Takuji Yamagami   +5 more
doaj   +1 more source

Plasma amyloid-beta levels correlated with impaired hepatic functions: An adjuvant biomarker for the diagnosis of biliary atresia

open access: yesFrontiers in Surgery, 2022
BackgroundBiliary atresia (BA) is an infantile fibro-obstructive cholestatic disease with poor prognosis. An early diagnosis and timely Kasai portoenterostomy (KPE) improve clinical outcomes. Aggregation of amyloid-beta (Aβ) around hepatic bile ducts has
Hongyu Lyu   +14 more
doaj   +1 more source

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