Literature DB >> 22813814

Partial internal biliary diversion for Alagille syndrome: case report and review of the literature.

Shari Sheflin-Findling1, Ronen Arnon, Samantha Lee, Jaime Chu, Fiona Henderling, Nanda Kerkar, Kishore Iyer.   

Abstract

This is a case report of the first patient with Alagille syndrome (AGS) to undergo a partial internal biliary diversion (PIBD) for the treatment of symptoms refractory to medical therapy. Alagille syndrome is a hereditary disease resulting in chronic cholestasis and hypercholesterolemia that can lead to severe and intractable pruritus and disfiguring and debilitating xanthomas. PIBD has proven to be an effective treatment option for other causes of cholestatic liver disease. This report reviews the immediate and 2-year follow-up of a patient after this surgical procedure. The results suggest that PIBD has potential to provide relief of intractable symptoms and improve the quality of life in patients with AGS while avoiding an external stoma. It does not, however, appear to prevent the progression of liver disease. Long-term follow-up is still needed.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22813814     DOI: 10.1016/j.jpedsurg.2012.04.008

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  2 in total

1.  Outcome of partial internal biliary diversion for intractable pruritus in children with cholestatic liver disease.

Authors:  P Ramachandran; N P Shanmugam; S Al Sinani; V Shanmugam; S Srinivas; M Sathiyasekaran; V Tamilvanan; M Rela
Journal:  Pediatr Surg Int       Date:  2014-07-27       Impact factor: 1.827

Review 2.  Alagille syndrome: clinical perspectives.

Authors:  Maha Saleh; Binita M Kamath; David Chitayat
Journal:  Appl Clin Genet       Date:  2016-06-30
  2 in total

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