Early Kasai portoenterostomy in a 9-day-old newborn with extrahepatic biliary atresia: a case report highlighting improved prognosis with prompt intervention

Extrahepatic biliary atresia (EHBA) is a leading cause of neonatal cholestasis, often resulting in end-stage cirrhosis and portal hypertension without early diagnosis and treatment. This report highlights the importance of timely intervention, describing a 6-day-old male newborn diagnosed with EHBA...

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Main Authors: Mortada H.F. El-Shabrawi, Gamal Eltagy, Mohamed Qinawy, Mohammed Am Oshi, Amjad Algethami, Nawaf A Alhujayri, Shaker S Alharthi, Abdullah M Alelyani, Naglaa M Kamal
Format: Article
Language:English
Published: SAGE Publishing 2025-02-01
Series:Journal of International Medical Research
Online Access:https://doi.org/10.1177/03000605241311115
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author Mortada H.F. El-Shabrawi
Gamal Eltagy
Mohamed Qinawy
Mohammed Am Oshi
Amjad Algethami
Nawaf A Alhujayri
Shaker S Alharthi
Abdullah M Alelyani
Naglaa M Kamal
author_facet Mortada H.F. El-Shabrawi
Gamal Eltagy
Mohamed Qinawy
Mohammed Am Oshi
Amjad Algethami
Nawaf A Alhujayri
Shaker S Alharthi
Abdullah M Alelyani
Naglaa M Kamal
author_sort Mortada H.F. El-Shabrawi
collection DOAJ
description Extrahepatic biliary atresia (EHBA) is a leading cause of neonatal cholestasis, often resulting in end-stage cirrhosis and portal hypertension without early diagnosis and treatment. This report highlights the importance of timely intervention, describing a 6-day-old male newborn diagnosed with EHBA who underwent successful Kasai portoenterostomy at 9 days of age. While the procedure is typically performed within the first 60 days of life, this exceptionally early intervention led to significantly improved outcomes. Postoperative recovery was marked by bilirubin normalization within 2 months and steady improvement in liver function tests, demonstrating the advantages of early surgery. The procedure involved creating a Roux-en-Y hepatic portojejunostomy to restore bile flow, preventing progression to biliary cirrhosis. Early intervention achieved effective bile drainage and substantial clinical improvement. At the 1-year follow-up, the infant displayed normal growth and liver function. This case supports the hypothesis that performing Kasai portoenterostomy earlier than current guidelines recommend may lead to better outcomes. It underscores the need for vigilant neonatal care to recognize early signs of cholestasis and enable prompt surgical intervention. Early diagnosis and intervention can preserve liver function, potentially delaying or preventing the need for liver transplantation.
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institution Kabale University
issn 1473-2300
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publishDate 2025-02-01
publisher SAGE Publishing
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series Journal of International Medical Research
spelling doaj-art-53e092f7459849de8b9bf3538cbf67722025-02-09T06:03:38ZengSAGE PublishingJournal of International Medical Research1473-23002025-02-015310.1177/03000605241311115Early Kasai portoenterostomy in a 9-day-old newborn with extrahepatic biliary atresia: a case report highlighting improved prognosis with prompt interventionMortada H.F. El-ShabrawiGamal EltagyMohamed QinawyMohammed Am OshiAmjad AlgethamiNawaf A AlhujayriShaker S AlharthiAbdullah M AlelyaniNaglaa M KamalExtrahepatic biliary atresia (EHBA) is a leading cause of neonatal cholestasis, often resulting in end-stage cirrhosis and portal hypertension without early diagnosis and treatment. This report highlights the importance of timely intervention, describing a 6-day-old male newborn diagnosed with EHBA who underwent successful Kasai portoenterostomy at 9 days of age. While the procedure is typically performed within the first 60 days of life, this exceptionally early intervention led to significantly improved outcomes. Postoperative recovery was marked by bilirubin normalization within 2 months and steady improvement in liver function tests, demonstrating the advantages of early surgery. The procedure involved creating a Roux-en-Y hepatic portojejunostomy to restore bile flow, preventing progression to biliary cirrhosis. Early intervention achieved effective bile drainage and substantial clinical improvement. At the 1-year follow-up, the infant displayed normal growth and liver function. This case supports the hypothesis that performing Kasai portoenterostomy earlier than current guidelines recommend may lead to better outcomes. It underscores the need for vigilant neonatal care to recognize early signs of cholestasis and enable prompt surgical intervention. Early diagnosis and intervention can preserve liver function, potentially delaying or preventing the need for liver transplantation.https://doi.org/10.1177/03000605241311115
spellingShingle Mortada H.F. El-Shabrawi
Gamal Eltagy
Mohamed Qinawy
Mohammed Am Oshi
Amjad Algethami
Nawaf A Alhujayri
Shaker S Alharthi
Abdullah M Alelyani
Naglaa M Kamal
Early Kasai portoenterostomy in a 9-day-old newborn with extrahepatic biliary atresia: a case report highlighting improved prognosis with prompt intervention
Journal of International Medical Research
title Early Kasai portoenterostomy in a 9-day-old newborn with extrahepatic biliary atresia: a case report highlighting improved prognosis with prompt intervention
title_full Early Kasai portoenterostomy in a 9-day-old newborn with extrahepatic biliary atresia: a case report highlighting improved prognosis with prompt intervention
title_fullStr Early Kasai portoenterostomy in a 9-day-old newborn with extrahepatic biliary atresia: a case report highlighting improved prognosis with prompt intervention
title_full_unstemmed Early Kasai portoenterostomy in a 9-day-old newborn with extrahepatic biliary atresia: a case report highlighting improved prognosis with prompt intervention
title_short Early Kasai portoenterostomy in a 9-day-old newborn with extrahepatic biliary atresia: a case report highlighting improved prognosis with prompt intervention
title_sort early kasai portoenterostomy in a 9 day old newborn with extrahepatic biliary atresia a case report highlighting improved prognosis with prompt intervention
url https://doi.org/10.1177/03000605241311115
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