Journal of Hepatology
Volume 51, Issue 3 , Pages 483-490, September 2009

Liver transplantation for glycogen storage disease type Ia

  • Srinevas K. Reddy

      Affiliations

    • Department of Surgery, Duke University Medical Center, Durham, NC, USA
  • ,
  • Stephanie L. Austin

      Affiliations

    • Department of Pediatrics, Duke University Medical Center, 595 LaSalle Street, Durham, NC 27710, USA
  • ,
  • Michele Spencer-Manzon

      Affiliations

    • Department of Pediatrics, Duke University Medical Center, 595 LaSalle Street, Durham, NC 27710, USA
  • ,
  • Dwight D. Koeberl

      Affiliations

    • Department of Pediatrics, Duke University Medical Center, 595 LaSalle Street, Durham, NC 27710, USA
  • ,
  • Bryan M. Clary

      Affiliations

    • Department of Surgery, Duke University Medical Center, Durham, NC, USA
  • ,
  • Dev M. Desai

      Affiliations

    • Department of Surgery, Duke University Medical Center, Durham, NC, USA
  • ,
  • Alastair D. Smith

      Affiliations

    • Department of Medicine, Duke University Medical Center, Durham, NC, USA
  • ,
  • Priya S. Kishnani

      Affiliations

    • Department of Pediatrics, Duke University Medical Center, 595 LaSalle Street, Durham, NC 27710, USA
    • Corresponding Author InformationCorresponding author. Tel.: +1 919 6811939; fax: +1 919 6848944.

Received 11 February 2009; received in revised form 4 April 2009; accepted 15 May 2009. published online 17 June 2009.

Associate Editor: P.A. Clavien

Background/Aims

Hepatocellular carcinoma (HCC) most often occurs within hepatocellular adenomas (HCAs) in glycogen storage disease Ia (GSD Ia) patients. The objective of this retrospective study is to assess outcomes after liver transplantation (LT) for GSD Ia where the principal indication for transplantation was prevention of HCC.

Methods

Petitions to the United Network for Organ Sharing region 11 review board for additional model for end-stage liver disease listing points were made on behalf of GSD Ia patients. Demographics, pre-operative comorbidity, and outcomes for GSD Ia patients who underwent LT were reviewed.

Results

Between 2004 and 2006, five GSD Ia patients underwent LT. Multiple HCAs with focal hemorrhage and/or necrosis but without histological evidence of malignancy were identified in all explanted specimens. Four of five patients had complications after LT, including cytomegalovirus (CMV) infections and steroid responsive allograft rejection. Hemoglobin levels and serum triglyceride, total cholesterol, blood glucose, and lactic acid concentrations improved in all patients after LT. Corn starch feeding was not required in any patient after LT. Renal function worsened in three patients despite modifications to primary immunosuppressive medications. All patients are alive at last follow-up (range 25–48 months) and all post-transplant complications have resolved.

Conclusions

By removing all possible adenomatous tissue and reversing the underlying hepatic enzymatic deficiency, LT provides definitive prevention against HCC and correction of most metabolic derangements in GSD Ia patients. Renal dysfunction secondary to GSD Ia persists—underscoring the need for further studies to better understand the mechanisms of renal dysfunction in these patients.

Abbreviations: GSD Ia, glycogen storage disease type Ia, HCC, hepatocellular carcinoma, HCA, hepatocellular adenoma, LT, liver transplantation, ESGSD I, European study on glycogen storage disease type I, MELD, model for end-stage liver disease, CT, computed tomography, MRI, magnetic resonance imaging, AFP, -fetoprotein

Keywords: Glycogen storage disease Ia, Liver transplantation, Hepatocellular adenoma, Hepatocellular carcinoma

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 The authors who have taken part in this study declared that they do not have anything to disclose regarding funding or conflict of interest with respect to this manuscript.

PII: S0168-8278(09)00396-1

doi:10.1016/j.jhep.2009.05.026

Journal of Hepatology
Volume 51, Issue 3 , Pages 483-490, September 2009