Volume 22, Issue 4 e13184
CASE REPORT

Biliary drainage as treatment for allograft steatosis following liver transplantation for PFIC-1 disease: A single-center experience

Leina S. Alrabadi

Leina S. Alrabadi

Department of Pediatrics, Section of Pediatric Gastroenterology and Hepatology, Yale University School of Medicine, New Haven, CT, USA

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Raffaella A. Morotti

Raffaella A. Morotti

Department of Pathology, Yale University School of Medicine, New Haven, CT, USA

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Pamela L. Valentino

Pamela L. Valentino

Department of Pediatrics, Section of Pediatric Gastroenterology and Hepatology, Yale University School of Medicine, New Haven, CT, USA

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Manuel I. Rodriguez-Davalos

Manuel I. Rodriguez-Davalos

Department of Surgery, Section of Transplantation and Immunology, Yale University School of Medicine, New Haven, CT, USA

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Udeme D. Ekong

Udeme D. Ekong

Department of Pediatrics, Section of Pediatric Gastroenterology and Hepatology, Yale University School of Medicine, New Haven, CT, USA

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Sukru H. Emre

Corresponding Author

Sukru H. Emre

Department of Surgery, Section of Transplantation and Immunology, Yale University School of Medicine, New Haven, CT, USA

Correspondence

Sukru Emre, Department of Surgery, Section of Transplantation and Immunology, Yale University School of Medicine, New Haven, CT, USA.

Email: [email protected]

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First published: 14 April 2018
Citations: 14

Abstract

Development of macrovesicular steatosis post–LT in patients with PFIC-1 is increasingly being observed, with the etiology not fully understood. We highlight successful and effective EBD for reversal of allograft steatosis in 2 patients with PFIC-1 disease and discuss our experience with internal biliary diversion in this patient population.

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