Abstract
Many of the inherited metabolic disorders affect the liver. However, outside specialist centres, most pathologists will see only a handful of cases in a working lifetime and thus only the commonest and best defined morphologically will be discussed in any detail in this section. More detailed accounts of these and rarer disorders are available elsewhere1–4.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Ishak, K. G. and Sharp, H. L. (1987). Metabolic errors and liver disease. In MacSween, R. N. M., Anthony, P. P. and Scheuer, P. J. (eds). Pathology of the liver. 2nd edn. pp. 99–180. Edinburgh: Churchill Livingstone
Filipe, M. I. and Lake, B. D. (1990). Histochemistry in Pathology. Edinburgh: Churchill Livingstone
Stanbury, B., Wyngarden, J. B., Fredrickson, D. S., Goldstein, J. L. and Brown, M. S. (eds.). (1983). The Metabolic Basis of Inherited Disease. 5th edn. New York: McGraw-Hill.
Ghishan, F. K. and Greene, H. L. (1990). Inborn errors of metabolism that lead to permanent liver injury. In Zakim, D. and Boyer, T. D. (eds). Hepatology. A textbook of liver disease. 2nd edn. pp. 1300–1348. Philadelphia: Saunders
James, S. P., Stomeyer, F. W. and Chang, C. (1981). Liver abnormalities in patients with Gaucher’s disease. Gastroeneterology, 80, 126–133
Wenger, D. A., Barth, G. and Githens, J. H. (1977). Nine cases of sphingomyelin lipidosis, a new variant in Spanish American children. Juvenile variant of Niemann-Pick disease with foamy and sea-blue histiocytes. Am. J. Dis. Child., 131, 955–961
Portmann, B. C. (1993). Paediatric liver disease. In Wight, D. G. D. (eds). Liver, Biliary Tract and Exocrine Pancreas. 3rd edn. Vol. 11. Systemic Pathology. Symmers, W. S. C. Series ed. Edinburgh: Churchill Livingstone
Beaudet, A. L., Ferry, G. D., Nichols, B. L. and Rosenberg, H. S. (1977). Cholesterol ester storage disease: clinical, biochemical and pathological studies. J. Pediatr., 90, 910–914
Bale, P. M., Clifton-Bligh, P., Benjamin, B. N. P. and Whyte, H. M. (1971). Pathology of Tangier disease. J. Clin. Pathol., 24, 609–616
Kelly, T. E. (1976). The mucopolysaccharidoses and mucolipidoses. Clin. Orthop., 114, 116–136
Spranger, J. (1975). Mucolipidoses 1. In Bergsma, D. (eds). Disorders of Connective Tissue. New York: Stratton Intercontinental Medical Book Corporation
McAdams, A. J., Hug, G. and Bove, K. E. (1974). Glycogen storage disease, types I to X. Criteria for morphological diagnosis. Hum. Pathol., 5, 463–487
Fink, A. S., Appleman, H. D. and Thompson, N. W. (1985). Hemorrhage into a hepatic adenoma and type la glycogen storage disease: a case report and review of the literature. Surgery, 97, 117–124
Segal, S. (1983). Disorders of galactose metabolism. In Stanbury, B., Wyngarden, J. B., Fredrickson, D. S., Goldstein, J. L. and Brown, M. S. (eds). The Metabolic Basis of Inherited Disease. 5th edn. pp. 161–191. New York: McGraw-Hill
Monk, A. M., Mitchell, A. J. H. and Milligan, D. W. A. (1977). The diagnosis of classical galactosaemia. Arch. Dis. Child., 52, 943–946
Gitzelman, R., Steinmann, B. and van den Berghe, G. (1983). Essential fructosuria, hereditary fructose intolerance, and fructose 1,6-diphosphatase deficiency. In Stanbury, B., Wyngarden, J. B., Fredrickson, D. S., Goldstein, J. L. and Brown, M. S. (eds). The Metabolic Basis of Inherited Disease. 5th edn. pp. 118–140. New York: McGraw-Hill
Schulte, M. J. and Lenz, W. (1977). Fatal sorbitol infusion in a patient with fructose-sorbitol intolerance [letter]. Lancet, 2, 188
Prive, L. (1967). Pathological findings in patients with tyrosinaemia. Can. Med. Assoc. J., 97, 1054–1056
Dehner, L. P., Snover, D. C., Sharp, H. L., Asher, N. A., Nakhleh, R. and Day, D. L. (1989). Hereditary tyrosinaemia type I (chronic form): Pathologic findings in the liver. Hum. Pathol., 20, 149–158
Author information
Authors and Affiliations
Rights and permissions
Copyright information
© 1993 D. G. D. Wight
About this chapter
Cite this chapter
Wight, D.G.D. (1993). Metabolic and Storage Disorders. In: Atlas of Liver Pathology. Current Histopathology, vol 23. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-2212-2_9
Download citation
DOI: https://doi.org/10.1007/978-94-011-2212-2_9
Publisher Name: Springer, Dordrecht
Print ISBN: 978-94-010-4980-1
Online ISBN: 978-94-011-2212-2
eBook Packages: Springer Book Archive