Results 41 to 50 of about 94,453 (216)
Frontiers in Immunology, 2021 Background and AimsBiliary atresia is the most common cause of liver disease and liver transplantation in children. The accumulation of bile acids in hepatocytes and the stimulation of the intestinal microbiome can aggravate the disease progression. This
Wei Song +17 more
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Role of high-frequency linear probe in ultrasound diagnosis of biliary atresia
Medical Journal of Dr. D.Y. Patil University, 2014 Cause of cholestatic jaundice in early infancy continues to be a diagnostic dilemma, with biliary atresia being the most common cause. Increasing age is a negative prognostic factor for biliary atresia.
Sanjay Khaladkar +3 more
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Biliary atresia: pathology, etiology and pathogenesis
Future Science OA, 2020 Biliary atresia is a progressive fibrosing obstructive cholangiopathy of the intrahepatic and extrahepatic biliary system, resulting in obstruction of bile flow and neonatal jaundice.
Mukul Vij, Mohamed Rela
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Review of redo-Kasai portoenterostomy for biliary atresia in the transition to the liver transplantation era [PDF]
, 2017 2017-08Portoenterostomy (PE) is the standard therapy for biliary atresia (BA). PE offers the chance of survival to children with BA. PE was the ultimate therapeutic modality for BA before liver transplantation (LT) was available.
Shirotsuki, Ryo +8 more
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Seminars in Pediatric Surgery, 2000 Although the prognosis of biliary atresia has been dramatically improved in the era of liver transplantation, the Kasai operation is still the first line of surgical treatment. Successful hepatic portoenterostomy depends on early diagnosis and surgery, adequate surgical technique, prevention of cholangitis, and precise postoperative management.
M, Nio, R, Ohi
openaire +2 more sources
Oral administration of eicosapentaenoic acid suppresses liver fibrosis in postoperative patients with biliary atresia [PDF]
, 2018 Purpose: Biliary atresia (BA) is characterized by progressive inflammation of the biliary system. This inflammation persists and causes liver fibrosis, although jaundice disappears after Kasai portoenterostomy (KP).
Chiba, Kosuke +10 more
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Changes of smooth muscle contractile filaments in small bowel atresia [PDF]
, 2012 AIM: To investigate morphological changes of intestinal smooth muscle contractile fibres in small bowel atresia patients. METHODS: Resected small bowel specimens from small bowel atresia patients (n = 12) were divided into three sections (proximal ...
Rolle, Udo +4 more
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Majalah Kedokteran Andalas, 2009 AbstrakAtresia bilier merupakan penyakit yang jarang terjadi dan penyababnya belum diketahui secara pasti. Karakteristik dari penyakit ini adalah terjadinya inflamasi progresif pada duktus bilier sehingga terjadi obstruksi ekstrahepatal yang akhirnya ...
Julinar Julinar +2 more
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Correctable biliary atresia and cholangiocarcinoma: a case report of a 63-year-old patient
Surgical Case Reports, 2019 Background Although cancer occurrence following surgery for biliary atresia has gradually increased, the development of cholangiocarcinoma in a native liver survivor of biliary atresia is extremely rare.
Masaki Nio +5 more
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Hepatolithiasis in a 52-year-old native liver survivor with postoperative biliary atresia
Journal of Pediatric Surgery Case Reports, 2023 Hepatolithiasis is well known to be a late complication after biliary reconstruction. However, there were few reports regarding hepatolithiasis in late complications of long-term, native liver survivors in postoperative patients of biliary atresia. Here,
Kazuki Shirane +5 more
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