{
  "abstract": "We report a rare case of biliary aplasia in an infant who presented with persistent jaundice and elevated direct bilirubin despite having cholic stools. Imaging confirmed the absence of extrahepatic bile ducts, consistent with biliary atresia. Intraoperatively, there was a complete absence of an extrahepatic biliary tree consistent with biliary hypoplasia. We identified a cryptogenic hepatic plate directly fused to the right portal vein on further dissection. Despite the atypical anatomy, a modified Kasai portoenterostomy was successfully performed. The patient showed progressive clinical improvement with complete resolution of jaundice and normalisation of liver function tests over the following months. This case underscores a rare anatomical variant that can still permit a favourable outcome with a timely Kasai procedure. To our knowledge, this is one of the few documented cases of hepatic plate–portal vein fusion in biliary atresia.",
  "authors": [
    {
      "affiliations": [
        "Division of Pediatric General, Thoracic and Fetal Surgery, Chidren's Hospital Univeristy of Missouri, Columbia, Missouri, USA"
      ],
      "name": "Yousef El-Gohary"
    },
    {
      "affiliations": [
        "Division of Pediatric Surgery, Department of Surgery, Mayo Clinic, Rochester, Minnesota, USA"
      ],
      "name": "Christopher R Moir"
    },
    {
      "affiliations": [
        "Division of Pediatric Surgery, Department of Surgery, University of Nebraska Medical Center and College of Medicine, Children’s Nebraska, Omaha, Nebraska, USA"
      ],
      "name": "Abdalla Zarroug"
    }
  ],
  "title": "Portohepatic fusion mimics biliary aplasia",
  "uid": "4e8c74ac-b16e-5349-bfdb-70cb1f8860ac"
}