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Subependymal giant cell astrocytoma

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Summary

Twenty-two cases of subependymal giant cell astrocytoma (SGCA), five of which associated with tuberous sclerosis, were reviewed by conventional neurohistological stains and by peroxidase-antiperoxidase (PAP) immunohistochemistry for glial fibrillary acidic (GFA) protein, the 68 Kd neurofilament subunit (68 Kd-NF), and neuron-specific enolase (NSE). Neurohistological stains confirmed the presence of PTAH-positive fibrils and the absence of Nissl bodies and of neurites originating from the tumor cells. GFA protein-positive cells were present in all tumors not associated with tuberous sclerosis. However, the number of positive cells in each tumor was highly variable. GFA protein-positive cells were rare in the two SGCA accompanying tuberous sclerosis and absent in the remaining three. Neurohistological stains showed no differences between GFA protein-positive and negative cells. 68 Kd-NF-positive cells were found in six tumors. In one tumor, associated with tuberous sclerosis, it was present in the large ganglion-like cells only. NSE-positive cells were found in 13 of 18 tumors examined, including four of the five SGCA associated with tuberous sclerosis. The significance of NSE-positivity in central neuroepithelial neoplasms in respect of their possible neuronal origin remains open.

This study suggests that the SGCA, especially those associated with tuberous sclerosis, include cells that are apparently unable to express GFA protein. Some of the tumor cells express the 68 Kd-NF, but this expression falls short of the complete expression of neuronal differentiation. The unique morphological appearances of the SGCA and the discrepancies reported in electron-microscopic and immunohistochemical studies suggest that the cell of origin of these tumors is the product of a dysgenetic event in early development. As a result, the potential of that cell for astrocytic or neuronal differentiation may be incompletely or aberrantly expressed, in particular when the stigmata of tuberous sclerosis are also present. No evidence of obvious ganglionic differentiation and no inference of a neuronal origin of the tumor cells in SGCA could be adduced from the present histochemical findings. This study supports the general interpretation of these tumors as a variant of astrocytoma.

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References

  1. Autilio-Gambetti L, Velasco ME, Sipple J, Gambetti P (1981) Immunochemical characterization of antisera to rat neurofilament subunits. J Neurochem 37:1260–1265

    Google Scholar 

  2. Bender BL, Yunis EJ (1980) Central nervous system pathology of tuberous sclerosis in children. Ultrastr Pathol 1:287–299

    Google Scholar 

  3. De Armond SJ, Eng LF, Rubinstein LJ (1980) The application of glial fibrillary acidic (GFA) protein immunohistochemistry in neurooncology. A progress report. Pathol Res Pract 168:374–394

    Google Scholar 

  4. De Chadarevian J-P, Hollenberg RD (1979) Subependymal giant-cell tumor of tuberose sclerosis. A light and ultrastructural study. Neuropathol Exp Neurol 38:419–433

    Google Scholar 

  5. Deck JHN, Eng LF, Bigbee J, Woodcock SM (1978) The role of glial fibrillary acidic protein in the diagnosis of central nervous system tumors. Acta Neuropathol (Berl) 42:183–190

    Google Scholar 

  6. Dhillon AP, Rode J, Leathem A (1982) Neurone specific enolase: an aid to the diagnosis of melanoma and neuroblastoma. Histopathology 6:81–92

    Google Scholar 

  7. Duffy PE, Huang Y-Y, Rapport MM, Graf L (1980) Glial fibrillary acidic protein in giant cell tumors of brain and other gliomas. Acta Neuropathol (Berl) 52:51–57

    Google Scholar 

  8. Eng LF, Bigbee JW (1978) Immunohistochemistry of nervous system-specific antigens. In: Agranoff BW, Aprison MH (eds) Advances in neurochemistry, vol 3. Plenum Press, New York, pp 43–98

    Google Scholar 

  9. Eng LF, Rubinstein LJ (1978) Contribution of immunohistochemistry to diagnostic problems of human cerebral tumors. J Histochem Cytochem 26:513–522

    Google Scholar 

  10. Ferraro A, Doolittle FJ (1936) Tuberous sclerosis (diffuse neurospongioblastosis). Psychiat Q 10:365–416

    Google Scholar 

  11. Globus JH (1938) Glioneuroma and spongioneuroblastoma, forms of primary neuroectodermal tumors of the brain. Am J Cancer 32:163–220

    Google Scholar 

  12. Ghobrial MW, Velasco ME, Koss ER (1983) Binding of neuron specific enolase (NSE) antibodies to mammalian cerebellums and human medulloblastoma. J Neuropathol Exp Neurol 42:313 [Abstr]

    Google Scholar 

  13. Haglid K, Carlsson CA, Stavrou D (1973) An immunological study of human brain tumors concerning the brain specific proteins S-100 and 14.3.2. Acta Neuropathol (Berl) 24:187–196

    Google Scholar 

  14. Hallervorden J, Krücke W (1956) Die tuberose Hirnsklerose. In: Lubarsch O, Henke F, Rössle R (Hrsg) Handbuch der speziellen pathologischen Anatomie und Histologie, Bd 13, Teil 4. Springer, Berlin, Göttingen, Heidelberg, S 602–633

    Google Scholar 

  15. Ludwin SK, Kosek JC, Eng LF (1976) The topographical distribution of S-100 and GFA protein in the adult rat brain: An immunohistochemical study using horseradish peroxidase-labeled antibodies. J Comp Neurol 165:197–207

    Google Scholar 

  16. Marangos PJ, Polak JM, Pearse AGE (1982) Neuron-specific enolase: a probe for neurons and neuroendocrine cells. Trends Neurosci 5:193–196

    Google Scholar 

  17. Marangos PJ, Schmechel D (1980) The neurobiology of the brain enolases. In: Youdim MBH, Lovenberg W, Sharman DF, Lagnado JR (eds) Essays in neurochemistry and neuropharmacology, vol 4. Wiley, New York, pp 211–247

    Google Scholar 

  18. Moore BW, Perez VJ (1968) Specific acidic proteins of the nervous system. In: Carlson FD (ed) Physiological and biochemical aspects of nervous integration. Prentice-Hall, Englewood Cliffs

    Google Scholar 

  19. Nakamura Y, Becker LE (1983) Subependymal giant-cell tumor: astrocytic or neuronal? Acta Neuropathol (Berl) 60:271–277

    Google Scholar 

  20. Ribadeau-Dumas JL, Poirier J, Escourolle R (1973) Etude ultrastructurale des lésions cérébrales de la sclérose tubéreuse de Bourneville. Acta Neuropathol (Berl) 25:259–270

    Google Scholar 

  21. Robertson DM, Hendry WS, Vogel FS (1964) Central ganglioneuroma: a case study using electron microscopy. J Neuropathol Exp Neurol 23:692–705

    Google Scholar 

  22. Roessmann U, Velasco ME, Gambetti P, Autilio-Gambetti L (1983) Neuronal and astrocytic differentiation in human neuroepithelial neoplasms. An immunohistochemical study. J Neuropathol Exp Neurol 42:113–121

    Google Scholar 

  23. Roussy G, Oberling C (1931) Les tumeurs des centres nerveux et des nerfs périphériques: Atlas du cancer, fasc 9 and 10. Alcan, Paris

    Google Scholar 

  24. Royds JA, Parsons MA, Taylor CB, Timperley WR (1982) Enolase isoenzyme distribution in the human brain and its tumours. J Pathol 137:37–49

    Google Scholar 

  25. Rubinstein LJ (1972) Tumors of the central nervous system. Atlas of tumor pathology, series 2, fasc 6. Armed Forces Institute of Pathology, Washington, DC

    Google Scholar 

  26. Rubinstein LJ (1982) Tumors of the central nervous system. Supplement. Atlas of tumor pathology, series 2, fasc 6. Armed Forces Institute of Pathology, Washington, DC

    Google Scholar 

  27. Rubinstein LJ, Herman MM (1972) A light- and electron-microscopic study of a temporal-lobe ganglioglioma. J Neurol Sci 16:27–48

    Google Scholar 

  28. Russell DS, Rubinstein LJ (1977) Pathology of tumours of the central nervous system, 4th edn. Williams and Wilkins, Baltimore

    Google Scholar 

  29. Schachner M, Hedley-Whyte ET, Hsu DW, Schoomaker G, Bignami A (1977) Ultrastructural localization of glial fibrillary acidic protein in mouse cerebellum by immunoperoxidase labeling. J Cell Biol 75:67–73

    Google Scholar 

  30. Schmechel D, Marangos PJ, Brightman M (1978) Neurone specific enolase is a molecular marker for peripheral and central neuroendocrine cells. Nature 276:834–836

    Google Scholar 

  31. Sima AAF, Robertson DM (1979) Subependymal giant-cell astrocytoma. J Neurosurg 50:240–245

    Google Scholar 

  32. Stefansson K, Wollmann R (1980) Distribution of glial fibrillary acidic protein in central nervous system lesions of tuberous sclerosis. Acta Neuropathol (Berl) 52:135–140

    Google Scholar 

  33. Stefansson K, Wollmann R (1981) Distribution of the neuronal specific protein, 14-3-2, in central nervous system lesions of tuberous sclerosis. Acta Neuropathol (Berl) 53:113–117

    Google Scholar 

  34. Sternberger, LA (1979) Immunocytochemistry, 2nd edn. Wiley, New York

    Google Scholar 

  35. Tapia FJ, Polak JM, Barbosa AJA, Bloom SR, Marangos PJ, Dermody C, Pearse AGE (1981) Neuron-specific enolase is produced by neuroendocrine tumors. Lancet I:808–811

    Google Scholar 

  36. Trombley IK, Mirra SS (1981) Ultrastructure of tuberous sclerosis: cortical tuber and subependymal tumor. Ann Neurol 9:174–181

    Google Scholar 

  37. Velasco ME, Dahl D, Roessmann U, Gambetti P (1980) Immunohistochemical localization of glial fibrillary acidic protein in human glial neoplasms. Cancer 45:484–494

    Google Scholar 

  38. Wick MR, Scheithauer BW, Kovacs K (1983) Neuron-specific enolase in neuroendocrine tumors of the thymus, bronchus, and skin. Am J Clin Pathol 79:703–707

    Google Scholar 

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Supported in part by research grant CA 31271 (LJR) from the National Cancer Institute, US Dept. of Health and Human Services

Dr. Bonnin is supported by Clinical Fellowship no. 5732 of the American Cancer Society and by Neuropathology Research Training grant T32 NS 07236 of the National Institute of Neurological and Communicable Diseases and Stroke, US Dept. of Health and Human Services

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Bonnin, J.M., Rubinstein, L.J., Papasozomenos, S.C. et al. Subependymal giant cell astrocytoma. Acta Neuropathol 62, 185–193 (1984). https://doi.org/10.1007/BF00691851

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