Results 31 to 40 of about 613,875 (232)

Simultaneous Hepatic Artery and Portal Vein Thrombosis After Kasai Portoenterostomy: A Rare but Life-Threatening Complication. [PDF]

Cureus
Biliary atresia (BA) is a progressive neonatal bile duct disease treated with the Kasai procedure; however, complications may necessitate liver transplantation.
Ptohis N, Kanna E, Batsari E, Lamprinou Z, Skondras I.   +4 more
europepmc   +2 more sources

Bacterial translocation markers and toll‐like receptors in biliary atresia following successful portoenterostomy

Acta Paediatrica, Volume 112, Issue 10, Page 2210-2217, October 2023., 2023
Abstract Aim The gut–liver axis may contribute to pathophysiology of cholestatic liver disorders like biliary atresia (BA) by bacterial translocation (BT). Toll‐like receptors (TLR) are pattern recognition receptors known to activate innate immunity and secretion of inflammatory cytokines.
Nimish Godbole, Antti Kyrönlahti, Maria Hukkinen, Marjut Pihlajoki, Markku Heikinheimo, Mikko P. Pakarinen   +5 more
wiley   +1 more source

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

Journal 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, Minu Bajpai, Kanika Sharma, Priyanka Naranje   +3 more
doaj   +1 more source

Overview of Biliary Atresia

대한영상의학회지, 2022
Biliary atresia is a progressive, idiopathic, obliterative disease of the extrahepatic biliary tree that presents with biliary obstruction in the neonatal period. It is the most common indication for liver transplantation in children.
Tae Yeon Jeon
doaj   +1 more source

Type 3 of progressive familial intrahepatic cholestasis (PFIC‐3): Case report

Clinical Case Reports, Volume 11, Issue 4, April 2023., 2023
Abstract Genetic testing should always be advised in both parents and children of families with progressive familial intrahepatic cholestasis as early detection will provide more options to a better qualitative life.
Mohammad Badr Almoshantaf, Suja Alasaad, Mhd Amin Alzabibi, Mosa Shibani, Weaam Ezzdean   +4 more
wiley   +1 more source

The Value of Hepatic Scintigraphy in the Diagnosis of Biliary Atresia

Frontiers 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, Patrick Ho Yu Chung, Kenneth Kak Yuen Wong   +2 more
doaj   +1 more source

MiR-100 rs1834306 A>G Increases Biliary Atresia Risk in Southern Han Chinese Children

BioMed Research International, Volume 2023, Issue 1, 2023., 2023
Background. Biliary atresia (BA) is a type of severe cholestatic childhood disease that may have a genetic component. miR-100 plays a key role in regulating cell apoptosis, proliferation, and inflammatory reactions. A single‐nucleotide polymorphism in miR-100 has been proven to modulate susceptibility to various diseases. Methods.
Jiaming Chang, Jiankun Liang, Chengwei Chai, Fei Liu, Boyuan Tao, Hezhen Wang, Yanlu Tong, Zhe Wang, Huimin Xia, Sercan Ergün   +9 more
wiley   +1 more source

‘Triangular Cord’ Sign in Biliary Atresia

대한영상의학회지, 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

Divergent expression of liver transforming growth factor superfamily cytokines after successful portoenterostomy in biliary atresia [PDF]

, 2019
Background: Pathogenesis of progressive liver fibrosis in biliary atresia after successful portoenterostomy remains unclear. We related hepatic expression of transforming growth factor beta (TGF-beta) superfamily cytokines to histologic liver injury ...
Lohi, Jouko, Kerola, Anna, Jalanko, Hannu, Pakarinen, Mikko P., Mutanen, Annika, Heikkilä, Päivi   +5 more
core   +1 more source

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

Frontiers 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, Yongqin Ye, Yongqin Ye, Vincent Chi Hang Lui, Vincent Chi Hang Lui, Weifang Wu, Weifang Wu, Patrick Ho Yu Chung, Patrick Ho Yu Chung, Kenneth Kak Yuen Wong, Kenneth Kak Yuen Wong, Hung-Wing Li, Man Shing Wong, Paul Kwong Hang Tam, Bin Wang   +14 more
doaj   +1 more source