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

SK Hourigan, RA Anders, SE Mitchell… - Pediatric …, 2012 - Wiley Online Library
SK Hourigan, RA Anders, SE Mitchell, KB Schwarz, H Lau, W Karnsakul
Pediatric transplantation, 2012Wiley Online Library
Hourigan SK, Anders RA, Mitchell SE, Schwarz KB, Lau H, Karnsakul W. Chronic diarrhea,
ascites, and protein‐losing enteropathy in an infant with hepatic venous outflow obstruction
after liver transplantation. 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 …
Hourigan SK, Anders RA, Mitchell SE, Schwarz KB, Lau H, Karnsakul W. Chronic diarrhea, ascites, and protein‐losing enteropathy in an infant with hepatic venous outflow obstruction after liver transplantation.
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.
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