Chronic diarrhea, ascites, and protein-losing enteropathy in an infant with hepatic venous outflow obstruction after liver transplantation

Pediatr Transplant. 2012 Nov;16(7):E328-31. doi: 10.1111/j.1399-3046.2012.01686.x. Epub 2012 Apr 10.

Abstract

An 18-month-old female status post-orthotopic liver transplant for biliary atresia presented nine months after transplant with severe diarrhea and intolerance of feeds. She was found to have a PLE as evidenced by a low serum albumin and a persistent elevation of fecal A1AT. Investigation eventually revealed that the cause of the PLE was a stricture at the anastomosis site between the hepatic vein and inferior cava, supported by resolution of the PLE after venoplasty of the stricture. The patient has subsequently required several repeat venoplasties for recurrence of her symptoms correlating with recurrence of the stricture. This is a very rare presentation of hepatic venous outflow obstruction. Moreover, normal duplex ultrasound imaging of liver vasculature and her unusual presentation led to a delay in her diagnosis highlighting the need for an increased index of suspicion.

Publication types

  • Case Reports

MeSH terms

  • Anastomosis, Surgical
  • Ascites / complications*
  • Ascites / etiology
  • Budd-Chiari Syndrome / complications
  • Budd-Chiari Syndrome / etiology*
  • Constriction, Pathologic
  • Diarrhea / complications*
  • Diarrhea / etiology
  • Female
  • Humans
  • Infant
  • Liver / diagnostic imaging
  • Liver / pathology
  • Liver Failure / complications*
  • Liver Failure / therapy
  • Liver Transplantation / adverse effects*
  • Postoperative Complications
  • Protein-Losing Enteropathies / complications*
  • Protein-Losing Enteropathies / etiology
  • Recurrence
  • Serum Albumin / metabolism
  • Ultrasonography / methods
  • Vascular Surgical Procedures / methods

Substances

  • Serum Albumin