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Striated adrenocortical cells in cerebro-hepato-renal (Zellweger) syndrome

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Summary

Adrenal glands from eight patients with the cerebro-hepatorenal syndrome, a disease in which there are no morphologically demonstrable peroxisomes, were studied histologically; one of the eight was also examined ultrastructurally. Seven of the eight demonstrated striated adrenocortical cells in the inner portion of the adrenal cortex. Ultrastructural examination confirmed that the striated cells contained the lammellae and lamellar-lipid profiles of very long chain fatty acids-cholesterol esters that are characteristic of adreno-leukodystrophy. This morphologic observation further emphasizes the common pathogenetic features of the cerebro-hepato-renal (Zellweger) syndrome and adreno-leukodystrophy.

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References

  • Baumbach J, Beard M, Cothran D, Steven S (1980) Isocitrate lyase and malate synthetase in the developing chick. J Cell Biol 87:324a

    Google Scholar 

  • Benke PJ, Reyes PF, Parker JC (1981) New form of adrenoleukodystrophy. Hum Genet 58:204–208

    Google Scholar 

  • Brown FR III, McAdams AJ, Cummins JW, Konkol R, Singh I, Moser AB, Moser HW (1982) Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acids. Johns Hopkins Med J 151:344–351

    Google Scholar 

  • Danks DM, Tippett P, Adams C, Campbell P (1975) Cerebro-hepato-renal syndrome of Zellweger. A report of eight cases with comments upon the incidence, the liver lesion, and a fault in pipecolic acid metabolism. J Pediatr 86:382–387

    Google Scholar 

  • Gatfield PD, Taller E, Hinton GG, Wallace AC, Abdelnour GM, Haust MND (1968) Hyperpipecolatemia: A new metabolic disorder associated with neuropathy and hepatomegaly. Can Med Assoc J 99:1215–1233

    Google Scholar 

  • Goldfischer S (1982) Peroxisomes and human metabolic diseases: The cerebro-hepato-renal syndrome (CHRS), cerebrotendinous xanthomatosis, and Schilder's disease (adrenoleukodystrophy). Ann NY Acid Sci 386:526–529

    Google Scholar 

  • Goldfischer S, Moore CL, Johnson AB, Spiro AJ, Valsamis MP, Wisniewski HK, Ritch RH, Norton WT, Rapin I, Garter LM (1973a) Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome. Science 182:62–64

    Google Scholar 

  • Goldfischer S, Johnson AB, Essner E, Moore C, Ritch RH (1973 b) Peroxisomal abnormalities in metabolic diseases. J Histochem Cytochem 21:972–977

    Google Scholar 

  • Haas JE, Johnson ES, Farrell DL (1982) Neonatal-onset adrenoleukodystrophy in a girl. Ann Neurol 12:449–457

    Google Scholar 

  • Igarashi M, Schaumburg HH, Powers JM, Kishimoto Y, Kolodny E, Suzuki K (1976) Fatty acid abnormality in adrenoleukodystrophy. J Neurochem 26:851–860

    Google Scholar 

  • Jaffe R, Crumrine R, Hashida Y, Moser HW (1982) Neonatal adrenoleukodystrophy. Clinical, pathological and biochemical delineation of a syndrome affecting both males and females. Am J Pathol 108:100–111

    Google Scholar 

  • Johnson AB, Schaumburg HH, Powers JM (1976) Histochemical characteristics of the striated inclusion of adrenoleukodystrophy. J Histochem Cytochem 24:725–730

    Google Scholar 

  • Jones RG, Davis WL (1982) The role of peroxisomes in the response of the toad bladder to aldosterone. Annals NY Acad Sci 386:165–168

    Google Scholar 

  • Kawamura N, Moser HW, Kishimoto YC (1981) Very long chain fatty acid oxidation in rat liver. Biochem Biophys Res Comm 99:1216–1225

    Google Scholar 

  • Kindl H, Lazarow PB (1982) Peroxisomes and Glyoxysomes. Ann NY Acad Sci, vol. 386, p 550

    Google Scholar 

  • Manz HJ, Schuelein M, McCullough DC, Kishimoto Y, Eiben RM (1980) New phenotype variant of adrenoleukodystrophy. Pathologic, ultrastructural and biochemical study in two brothers. J Neurol Sci 45:245–260

    Google Scholar 

  • Müller-Höcker J, Bise K, Endres W, Hübner G (1981) Zur Morphologie und Diagnostik des Zellweger Syndroms. Ein Beitrag zum kombiniert cytochemisch-feinstrukturellen Nachweis der Peroxisomen in autopischem und tiefgefrorenem Lebergewebe mit Fallbericht. Virchows Arch [Pathol Anat] 393:103–114

    Google Scholar 

  • Opitz JM, ZuRhein GM, Vitale L, Shahidi, Howe JJ, Chou SM, Shanklin DR, Sybers HD, Dood AR, Gerritsen T (1969) The Zellweger syndrome (cerebro-hepato-renal syndrome) birth defects: Birth Defects: Original Article Series 5:144–160

    Google Scholar 

  • Osmundsen H (1982) Peroxisomal B-oxidation of long fatty acids: effects of high fat diets. Ann NY Acad Sci 386:13–27

    Google Scholar 

  • Partin JS, McAdams AJ (1983) Absence of hepatic peroxisomes in neonatal onset adrenoleukodystrophy. Pediatr Res 17:294

    Google Scholar 

  • Pfeifer U, Sandhage K (1979) Licht- und Elektronenmikroskopische Leberbefunde beim Cerebro-Hepato-Renalen Syndrom nach Zellweger (Peroxisomen-Defizienz). Virchows Arch [Pathol Anat] 384:269–284

    Google Scholar 

  • Powers JM, Schaumburg HH (1973) The adrenal cortex in adrenoleukodystrophy. Arch Pathol 96:305–310

    Google Scholar 

  • Powers JM, Schaumburg HH, Johnson AB, Raine CS (1980) A correlative study of the adrenal cortex in adreno-leukodystrophy- evidence for a fatal intoxication with very long chain saturated fatty acids. Invest Cell Pathol 3:353–376

    Google Scholar 

  • Powers JM, Moser HW, Moser AB, Schaumburg HH (1982) Fetal adrenoleukodystrophy: The significance of pathologic lesions in adrenal gland and testis. Hum Pathol 13:1013–1019

    Google Scholar 

  • Schaumburg HH, Powers JM, Raine CS, Suzuki K, Richardson EP (1975) Adrenoleukodystrophy. A clinical and pathological study of 17 cases. Arch Neurol 32:577–591

    Google Scholar 

  • Schaumburg HH, Powers JM, Raine CS, Spencer PS, Griffin JW, Prineas JW, Boehme D (1977) Adrenomyeloneuropathy - a possible variant of adrenoleukodystrophy, Part 2 (general pathologic, neuropathologic and biochemical aspects). Neurology 27:1114–1119

    Google Scholar 

  • Ulrich J, Herschkowitz N, Heitz P, Sigrist T, Baerlocher P (1978) Adrenoleukodystrophy: Preliminary report of a neonatal case. Light and electron microscopical, immunocytochemical biochemical findings. Acta Neuropathol (Berlin) 43:77–83

    Google Scholar 

  • Versmold HT, Bremer HJ, Herzog V, Siegel G, v Bassewitz DB, Irle V, v Voss H, Lombeck J, Brauser B (1977) A metabolic disorder similar to Zellweger's syndrome with hepatic acatalasia and absence of peroxisomes, altered content and redox state of cytochromes, and infantatile cirrhosis with hemosiderosis. Eur J Pediatr 124:261–275

    Google Scholar 

  • Volpe JJ, Adams RD (1972) Cerebro-hepato-renal syndrome of Zellweger: An inherited disorder of neuronal migration. Acta Neuropathol (Berlin) 20:175–179

    Google Scholar 

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Supported in part by Grants HL 21756 and NIAMD 17702

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Goldfischer, S., Powers, J.M., Johnson, A.B. et al. Striated adrenocortical cells in cerebro-hepato-renal (Zellweger) syndrome. Vichows Archiv A Pathol Anat 401, 355–361 (1983). https://doi.org/10.1007/BF00734851

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