The Zellweger syndrome: subcellular pathology, neuropathology, and the demonstration of pneumocystis carinii pneumonitis in two siblings
- 55 Downloads
- 14 Citations
Abstract
The first Scandinavian cases of Zellweger syndrome (ZS) are described. A brother and sister, children of first cousins, had the typical clinical symptoms and pathological findings. Extensive metabolic studies in the boy were negative. Pipecolic acid in the urine was not elevated. Both children died at 14 weeks of age. Two months earlier the girl had suffered severe intestinal bleeding. Both had pneumocystic carinii pneumonia at autopsy although no evidence of immune deficiency had been found in the boy. The girl had used up her visible iron depots while the boy still had abundant but probably physiologic amounts of hemosiderin in the RES. Most of the cerebral abnormalities are unspecific and possibly related to anoxia or other causes of delayed maturation. The white matter abnormalities in ZS patients may only be quantitatively different from the common “fatty metamorphosis” in infants. Previously reported ultrastructural abnormalities (absence of peroxisomes and very sparse smooth endoplasmic reticulum, as well as mitochondrial abnormalities) which are possibly unique for ZS, are confirmed. It is stressed that these were seen despite phenobarbital treatment which normally stimulates the formation of smooth endoplasmic reticulum.
Key words
Zellweger (cerebro-hepato-renal) syndrome Hypotonia Cerebral malformations Retarded maturation Sudanophilic leucoencephalopathy Mitochondria Peroxisomes Phenobarbital Iron metabolism Pneumocystis carinii pneumoniaPreview
Unable to display preview. Download preview PDF.
References
- 1.Agamonolis, D. P., Robinson, H. B., Timmons, G. D.: Cerebro-hepato-renal syndrome. Report of a case with histochemical and ultrastructural observation. J. Neuropath. Exp. Neurol. 35, 220–246 (1976)Google Scholar
- 2.Bowen, P., Lee, C. S. N., Zellweger, H., Lindenberg, R.: A familial syndrome of multiple congenital defects. Bull. John Hopk. Hosp. 114, 402–414 (1962)Google Scholar
- 3.Brun, A.: The subpial granular layer of the foetal cerebral cortex in man. Its ontogeny and significance in congenital cortical malformations. Acta Path. Microbiol. Scand. Suppl. 179, 1–98 (1965)Google Scholar
- 4.Danks, D. M., Tippett, P., Adams, C., Campbell, P.: Cerebro-hepato-renal syndrome of Zellweger. J. Pediat. 86, 382–387 (1975)Google Scholar
- 5.Donohue, W.: Interstitial plasma cell pneumonia. Labor. Invest. 5, 97–105 (1956)Google Scholar
- 6.Ernster, L., Orrenius, S.: Dynamic organization of endoplasmic reticulum membranes. Drug. Metab. Dispos. 1, 66–73 (1973)Google Scholar
- 7.Essner, E.: Endoplasmic reticulum and the origin of microbodies in the fetal mouse liver. Labor. Invest. 17, 71–87 (1967)Google Scholar
- 8.Friede, R. L.: Diffuse fatty change of the white matter. In: Developmental nervous pathology, p. 51. Wien-New York: Springer 1975Google Scholar
- 9.Gilchrist, K. W., Gilbert, E. F., Goldfarb, S., Goll, U., Spranger, J. W., Opitz, J. M.: Studies of malformation syndromes of man XI B: The cerebro-hepato-renal syndrome of Zellweger: Comparative pathology. Europ. J. Pediat. 121, 99–118 (1976)Google Scholar
- 10.Goldfischer, S., Moore, C. L., Johnson, A. B., Spiro, A. T., Valsamis, M. P., Wisniewski, H. K., Ritch, R. H., Norton, W. T., Rapin, I., Garner, L. M.: Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome. Science 182, 62–64 (1973)Google Scholar
- 11.Hackenbroch, Ch. R.: Chemical and physical fixation of isolated mitochondria in lowenergy and high-energy states. Biochemistry 61, 598–605 (1968)Google Scholar
- 12.Huges, J. B., Price, R. A., Sisko, F., Havorn, W. S., Kafatos, A. G., Schonland, M., Smythe, P. M.: Protein-caloric malnutrition, a host determinant for Pneumocystis carinii infection. Am. J. Dis. Child. 128, 44–45 (1974)Google Scholar
- 13.Karlberg, P., Taranger, J., Engström, L., Lichtenstein, H., Svennberg-Redegren, I.: The somatic development of children in a Swedish urban community. Acta Paediat. Scand. Suppl. 258, 27–28 (1976)Google Scholar
- 14.Langley, F. E.: Haemopoiesis and siderosis in the foetus and newborn. Arch. Dis. Childh. 26, 64–75 (1951)Google Scholar
- 15.Leech, R. W., Alvord, E. C.: Glial fatty metamorphosis. An abnormal response of premyelin glia frequently accompanying periventricular leukomalacia. Am. J. Path. 74, 603–610 (1974)Google Scholar
- 16.Liu, H. M., Bangaru, B. S., Kidd, J., Boggs, J.: Neuropathological considerations in cerebrohepato-renal syndrome (Zellweger's syndrome). Acta Neuropath. 34, 115–123 (1976)Google Scholar
- 17.Marver, H. S.: The role of heme in the synthesis and repression of microsomal protein. In: Microsomes and drug oxidations, J. R. gillette A. H. Conney, G. J. Cosmides, R. W. Estebrook, J. R. Fouts, G. J. Mannering, eds., pp. 495–511. New York: Academic Press 1969Google Scholar
- 18.Novikoff, A. B., Shin, W. Y.: The endoplasmic reticulum in the Golgi zone and its relations to microbodies, Golgi apparatus and autophagic vacuoles in rat liver cells. J. Microscopie 3, 187–206 (1964)Google Scholar
- 19.Passarge, E., McAdams, A. J.: Cerebro-hepato-renal syndrome. A newly recognized hereditary disorder of multiple congenital defects including sudanophilic leukodystrophy, cirrhosis of liver and polycystic kidneys. J. Pediat. 71, 691–702 (1967)Google Scholar
- 20.Patton, R. G., Christie, D. L., Smith, D. W., Beckwith, J. B.: Cerebro-hepato-renal syndrome of Zellweger. Am. J. Dis. Child. 124, 840–844 (1972)Google Scholar
- 21.Pavlica, F.: The first observation of congenital pneumocystic pneumonia in a fully developed stillborn child. Ann. paediat. 198, 177–184 (1962)Google Scholar
- 22.Robbins, J. B.: Pneumocystic Carinii Pneumonitis, a review. Pediat. Res. 1, 131–158 (1967)Google Scholar
- 23.Safouh, M., Crocker, F. S., Vernier, R.: Experimental cystic disease of the kidney. Labor. Invest. 23, 392–400 (1970)Google Scholar
- 24.Seip, M., Halvorsen, S.: Erythrocyte production and iron stores in premature infants during the first months of life. Acta Paediat. Scand. 45, 600–617 (1956)Google Scholar
- 25.Smith, D. W., Opitz, J. M., Inhorn, S. L.: A syndrome of multiple development defects including polycystic kidneys and intrahepatic biliary dysgenesis in 2 siblings. J. Pediat. 67, 617–624 (1965)Google Scholar
- 26.Smith, N. J., Rosells, S., Say, M. B., Yeya, K.: Iron storage in the first five years of life. Pediatrics 16, 166–171 (1955)Google Scholar
- 27.Tephly, T. R., Webb, C., Trusslev, P., Kniffen, F., Hasegawa, E., Piper, W.: The regulation of hemesynthesis related to drug metabolism. Drug Metab. and Dispos. 1, 259–266 (1973)Google Scholar
- 28.Thaler, M., Dallman, P. R., Goodman, J.: Phenobarbital-induced changes in NADPH-cytochrome C reductase and smooth-endoplasmic reticulum in human liver. J. Pediat. 80, 302–310 (1972)Google Scholar
- 29.Trump, B. F., Laiho, K. A., Mergner, J., Arstila, A. U.: Studies on the subcellular pathophysiology of acute lethal cell injury. Beitr. Path. Bd. 152, 243–271 (1974)Google Scholar
- 30.Versmold, H. T., Bremer, H. J., Herzog, V., Siegel, G., Bassewitz, B. v., Irle, U., Voss, H. v., Lombeck, I., Brauser, B.: A metabolic disorder similar to Zellweger syndrome with hepatic acatalasia and absence of peroxisomes, altered content and redox state of cytochromes and infantile cirrhosis with hemsideros. Europ. J. Pediat. 124, 261–275 (1977)Google Scholar
- 31.Volpe, J. J., Adams, R. D.: Cerebro-hepato-renal syndrome of Zellweger. An inherited disorder of neuronal migration. Acta Neuropath. 20, 175–198 (1972)Google Scholar
- 32.Williams, J. P., Secrist, L., Fowler, G. W., Gwinn, J. L., Dumars, K. G.: Roentgenographic features of the cerebrohepatorenal syndrome of Zellweger. Am. J. Roentgenol. Radium Ther. Nucl. Med. 115, 607–610 (1972)Google Scholar