Journal of Inherited Metabolic Disease

, Volume 14, Issue 5, pp 831–832 | Cite as

Peliosis hepatis with type I glycogen storage disease

  • H. Schmidt
  • K. Ullrich
  • H. -J. von Lengerke
  • P. E. Peters
Case Report

Keywords

Liver Parenchyma Glycogen Storage Disease Dietary Therapy Glycogen Storage Disease Type Lithocholic Acid 

References

  1. Baheri, S. A., Palmer, R. H., Boyer, J. L. and Hunter, R. L. Production of peliosis hepatis in mice by the oral administration of sodium lithocholate.Gastroenterology 64 (1973) 879Google Scholar
  2. Bergs, V. V. and Scotti, T. M. Virus-induced peliosis hepatis in rats.Science 158 (1967) 377–378PubMedCrossRefGoogle Scholar
  3. Leveille, G. A., King, N. W., Sauberich, H. E. and Fairchild, D. G. Introduction and regression of biochemical and morphologic changes induced by dietary lithocholic acid in chicken.Am. J. Vet. Res. 27 (1966) 1045–1052PubMedGoogle Scholar
  4. Lyon, J., Bookstein, J. J., Sautwright, C. A., Romano, A. and Heeney, D. J. Peliosis hepatis: Diagnosis by magnification wedged hepatic venography.Radiology 150 (1984) 647–649PubMedGoogle Scholar
  5. Spycher, M. A. and Gitzelmann, R. Glycogenosis type I (glucose-6-phosphatase deficiency): Ultrastructural alterations of hepatocytes in a tumor bearing liver.Virchows Arch. Abt. B. Zellpath. 8 (1971) 133–142Google Scholar

Copyright information

© SSIEM and Kluwer Academic Publishers 1991

Authors and Affiliations

  • H. Schmidt
    • 1
  • K. Ullrich
    • 2
  • H. -J. von Lengerke
    • 3
  • P. E. Peters
    • 3
  1. 1.Department of Pediatrics Joh. Gutenberg-UniversityMainzGermany
  2. 2.Department of PediatricsMünsterGermany
  3. 3.Radiology Westf. Wilhelms-UniversityMünsterGermany

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