Summary
In the adrenal cortex of newborn infants there can occasionally be found distinct, large cells with large, prominent nuclei. This penomenon of “adrenal cytomegaly” has not been satisfactorily explained. In a series of 300 necropsies of infants up to 10 days of age “cytomegalic” cells were found in 16 instances. In 11 of these there was serological or pathological evidence of Rh-incompatibility, but in the remaining five instances no such evidence was found. There were, however, various congenital abnormalities. The morphological features of the large adrenal cells raised the possibility that these cells were polyploid. The suggestion is advanced that adrenal cytomegaly is a non-specific phenomenon, a response to intense, prolonged stimulation for a variety of reasons, which produces changes in the endocellular structure that manifest themselves as polyploidy. The hypothesis put forward here can account better for the occurrence of adrenal cytomegaly in a number of seemingly unrelated conditions than the other explanations of this phenomenon advanced so far.
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Aguilar, M. J., Kamoshita, S., Landing, B. H., Boder, E., Sedgwick, R. P.: Pathological observations in ataxia-telangiectasia. A report on five cases. J. Neuropath. exp. Neurol.27, 659–676 (1968).
Bachmann, R.: Die Nebenniere. In: Handbuch der mikroskopischen Anatomie des Menschen, ed.: W. Bargmann, vol. V, Die Nebenniere. Berlin-Göttingen-Heidelberg: Springer 1954.
Baker, de C., Wise, G., Mezger, M. L.: Cytomegalic adrenal hypoplasia in a 4 1/2-year-old boy. Amer. J. Dis. Child.114, 180–185 (1967).
Bayer, A., Židová, L., Dušek, J.: Zum Vorkommen von Riesenzellen in den Kindernebennieren. Zbl. allg. Path. path. Anat.104, 27–34 (1962).
Beatty, E., Hawes, C. R.: Cytomegaly of the adrenal gland. Amer. J. Dis. Child.89, 463–467 (1955).
Beckwith, B. J.: Macroglossia, omphalocele, adrenal cytomegaly, gigantism and hyperplastic visceromegaly. Birth Defects, Original Article Series, 5, No 2, 188–196, February (1969).
Borit, A., Kosek, J.: Cytomegaly of the adrenal cortex. Electron microscopy in Beckwith's syndrome. Arch. Path.88, 58–64 (1969).
Bull, L. B.: The histological evidence of liver damage from pyrrolizidine alkaloids: Megalocytosis of the liver cells and inclusion globules. Aust. vet. J.30, No 1, 33–40, January (1954).
—— Dick, A. T.: The chronic pathological effects on the liver of the rat of the pyrrolizidine alkaloids heliotrine, lasiocarpine and their n-oxides. J. Path. Bact.78, 482–502 (1959).
Chute, A. L., Robinson, G. C., Donahue, W. L.: Cushing's syndrome in children. J. Pediat.34, 20–39 (1949).
Cohen, R. B., Chapman, W. B., Castleman, B. J.: Hyperadrenocorticism (Cushing's disease). A study of surgically resected adrenal glands. Amer. J. Path.35, 5237–561 (1959).
Craig, J. M., and Landing, B. H.: Anaplastic cells of fetal adrenal cortex. Amer. J. clin. Path.21, 940–949 (1951).
Deamer, W. C., Silver, H. K.: Abnormalities in the secretion of the adrenal cortex during early life. J. Pediat.37, 490–516 (1950).
de Jong, B.: Polyploidy in animals. Bibliographia Genet.92, 111–228 (1957).
Dhom, G.: Die Nebennierenrinde im Kindesalter. Orthologie und Pathologie. Berlin-Heidelberg-New York: Springer 1965.
—— Städtler, F.: Morphologische Befunde an der Nebennierenrinde bei primärem Aldosteronismus. Virchows Arch. Abt. A345, 176–199 (1968).
Diamond, I., Anderson, M., McCreadie, S. R.: Transplacental transmission of busulfan (myleran) in a mother with leukemia. Production of fetal malformation and cytomegaly. Pediat.25, 85–90 (1960).
Dietrich, A., Siegmund, H.: Die Nebenniere und das chromaffine System (Paraganglien, Karotisdrüse, Steißdrüse). In: Handbuch der speziellen pathologischen Anatomie und Histologie, ed.: F. Henke and O. Lubarsch, vol. 8, Drüsen mit innerer Sekretion. Berlin: Springer 1926.
Gabe, M., Arvy, L.: Gland cells. In: The cell, ed.: Brachet and Mirsky, vol. 5. New York: Academic Press 1961.
Garneau, R.: La cytomégalie des glandes surrénales. Maladie à virus. Ann. Anat. path.2, 104–108 (1957).
Gasser, C.: Hemolytic anemia in premature babies with spontaneous appearance of Heinz bodies. Quart. Rev. Pediat.9, No 1, 12–13 (1954).
Geitler, L.: In: Protoplasmatologie, Handbuch der Protoplasmaforschung, ed.: L. V. Heilbrunn and F. Weber, VI–C Wien: Springer 1953.
Guttman, P. H.: Addison's disease. A statistical analysis of 566 cases and a study of the pathology. Arch. Path.10, 742–785 (1930).
Harlem, O. K., Myhre, E.: Congenital adrenal hypoplasia. Amer. J. Dis. Child.94, 696–701 (1957).
Irving, I. M.: Exomphalos with macroglossia. A study of eleven cases. J. pediat. Surg.2, No 6, 499–507 (1967).
Jago, M. V.: The development of the hepatic megalocytosis of chronic pyrrolizidine alkaloid poisoning. Amer. J. Path.56, 405–522 (1969).
Kampmeier, O. F.: Giant epithelial cells of the human fetal adrenal. Anat. Rec.37, 95–102 (1927).
Kerenyi, N.: Congenital adrenal hypoplasia. Report of a case with extreme adrenal hypoplasia and neurohypophyseal aplasia, drawing attention to certain aspects of etiology and classification. Arch. Path.71, 336–343 (1961).
Kiefer, H.: Addisonsche Erkrankung infolge chronischer Nebennierendystrophie mit adenomartigen Regeneraten. Virchows Arch. path. Anat.265, 472–489 (1927).
Kissane, J. M., Smith, M. G.: Pathology of infancy and childhood. St. Louis: C. V. Mosby 1967.
Kracht, J., Tamm, J.: Bilaterale kleinknotige Adenomatosis der Nebennierenrinde bei Cushing-Syndrom. Virchows Arch. path. Anat.333, 1–9 (1960).
Landing, B. H.: Studies on the anatomy of the human adrenal cortex in various functional states. In: The human adrenal cortex. Ciba Foundation Colloquia on Endocrinology, vol. 8, p. 52–66 (1955). London: J. & A. Churchill Limited 1955.
Le Breton, E., Moule, Y.: Biochemistry and physiology of the cancer cell. In: The cell, ed.: Brachet and Mirsky, vol. 5. New York: Academic Press 1961.
Luse, S.: Fine structure of adrenal cortex. In: The adrenal cortex, ed.: Eisenstein, A. B. Boston: Little, Brown and Co. 1967.
MacMahon, H. E., Wagner, R., Weiner, D. B.: Acute adrenal insufficiency due to congenital defect. Amer. J. Dis. Child.94, 282–285 (1957).
Mitchell, R. G., Rhaney, K.: Congenital adrenal hypoplasia in siblings. LancetI, 488–492 (1959).
Morison, J. E.: Foetal and neonatal pathology. Washington: Butterworths 1963.
Oppenheimer, E. H.: Adrenal cytomegaly studies by light and electron microscopy. Comparison with the adrenal in Beckwith's and virilism syndromes. Arch. Path.90, No 1, 57–64 (1970).
Pehlemann, R. W., Hanke, W.: Funktionsmorphologie des Interrenalorgans vonRana temporaria L. Z. Zellforsch.89, 281–302 (1968).
Potter, E. L.: Pathology of the fetus and the newborn, second ed. Chicago: Year Book Medical Publications Inc. 1961.
Rather, L. J.: The significance of nuclear size in physiological and pathological processes. Ergebn. allg. Path. path. Anat.38, 127–199 (1958).
Russfield, A. B.: The endocrine glands after bilateral adrenalectomy compared with those in spontaneous adrenal insufficiency. Cancer (Philad.)8, 523–537 (1955).
Schoental, R., Bensted, J. P. M.: Effects of whole body irradiation and of partial hepatectomy on the liver lesions induced in rats by a single dose of retrorsine, a pyrrolizidine (Senecio) alkaloid. Brit. J. Cancer17, 242–251 (1963).
—— Magee, P. N.: Further observations on the subacute and chronic liver changes in rats after a single dose of various pyrrolizidine (Senecio) alkaloids. J. Path. Bact.78, 471–482 (1959).
Selye, H., Stone, H.: On the experimental morphology of the adrenal cortex. American Lecture Series. Springfield, Ill.: Charles C. Thomas 1950.
Sherman, F. E., Bass, L. W., Fetterman, G. H.: Congenital metastasizing adrenal cortical carcinoma associated with cytomegaly of the fetal adrenal cortex. Amer. J. clin. Path.30, 439–446 (1958).
Šikl, H.: Addison's disease due to congenital hypoplasia of adrenals in an infant aged 33 days. J. Path. Bact.60, 323–324 (1948).
Singer, D. B., Rudolph, A. J., Rosenberg, H. S., Rawls, W. E., Boniuk, M.: Pathology of the congenital rubella syndrome. J. Pediat.71, No 5, 665–675 (1967).
Sotelo-Avila, S., Singer, D. B.: Syndrome of hyperplastic fetal visceromegaly and neonatal hypoglycemia (Beckwith's syndrome). Pediatrics.46, No 2, 240–251 (1970).
Stark, E., Palkovits, M., Fachet, J., Hajtman, B.: Adrenocortical nuclear volume and adrenocortical function. Acta med. Acad. Sci. hung.21, 263–269 (1965).
Steinbiss, W.: Über eine eigenartige Degeneration der Nebennieren bei Addisonscher Krankheit. Virchows Arch. path. Anat.262, 286–297 (1926).
Stowens, D.: Pediatric pathology, second ed. Baltimore: Williams & Wilkins Co. 1966.
Therien, B., Mellinger, R. C., Caldwell, J. R., Howard, P. J.: Primary aldosteronism due to adrenal hyperplasia. Occurrence in a boy aged 10 years. Amer. J. Dis. Child.98, 90–99 (1959).
Tonutti, E., Bayer, J. M., Spiegelhoff, W.: Beitrag zur Kenntnis der Struktur der Nebennierenrinde beim connatalen adrenogenitalen Syndrom. Endokrinologie40/41, 310–335 (1960/61).
Uotila, U. U.: The early embryological development of the fetal and permanent adrenal cortex in man. Anat. Rec.96, 183–203 (1940).
Wägelin, C.: Schilddrüse. Drüsen mit innerer Sekretion. In: Handbuch der speziellen pathologischen Anatomie und Histologie, ed.: F. Henke and O. Lubarsch. Berlin: Springer 1926.
Wells, H. G.: Addison's disease with selective destruction of suprarenal cortex (suprarenal cortex atrophy). Arch. Path.10, 499–523 (1930).
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Aterman, K., Kerenyi, N. & Lee, M. Adrenal cytomegaly. Virchows Arch. Abt. A Path. Anat. 355, 105–122 (1972). https://doi.org/10.1007/BF00556313
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DOI: https://doi.org/10.1007/BF00556313