Skip to main content
Log in

Cytoplasmic inclusions of astrocytic elements of glial tumors: special reference to round granulated body and eosinophilic hyaline droplets

  • Regular Paper
  • Published:
Acta Neuropathologica Aims and scope Submit manuscript

Abstract

Round granulated body (RGB) and eosinophilic hyaline droplets (EHDs) have been described as cytoplasmic inclusions of certain astrocytic tumors. In the previous literature, however, these inclusions have been described using various terms or regarded as nosologically the same entity. Light microscopically, RGB apeared as a round discrete body filled with fine uniform granules, while EHDs demonstrated a cluster of bright eosinophilic, round objects of various size. They could be clearly distinguished even by conventional histochemical staining such as the Masson trichrome stain and the phosphotungstic acid hematoxylin preparation. Both RGB and EHDs expressed positive immunoreactions for glial fibrillary acidic protein, several lysosomal markers, and some stress-response proteins. The ultrastructural appearances of these inclusions were distinct, however, one common feature was that they consisted of aggregations of numerous membrane-bound electron-dense bodies. Thus, both inclusions appear to be produced by neoplastic astrocytes and are possibly related to the lysosomal system. We examined the presence of RGB and EHDs in 138 astrocytic tumors. Both inclusions occurred most frequently in pleomorphic xanthoastrocytomas, followed by gangliogliomas and pilocytic astrocytomas. Subependymal giant cell astrocytomas exhibited only RGBs. RGBs and EHDs were not seen in any abundance in glioblastomas, gliosarcomas, fibrillary astrocytomas, protoplasmic astrocytomas, or oligo-astrocytomas. Some glioblastomas, however, showed only EHDs in small numbers. Several anaplastic astrocytomas were associated with a large number of RGBs and/or EHDs, and they revealed only rare mitosis despite marked cellular pleomorphism. Although RGB and EHDs have different morphological features, the presence of these inclusions in abundance may represent either a degenerative change, a long-standing lesion, or an indolent growth of the astrocytic tumors.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Allegranza A, Ferraresi S, Bruzzone M, Giombini S (1991) Cerebromeningeal pleomorphic xanthoastrocytoma. Report of four cases: clinical, radiological and pathological features (including a case with malignant evolution). Neurosurg Rev 14: 43–49

    Google Scholar 

  2. Arai N, Yagishita S, Amano N, Iwabuchi K, Misugi K (1989) “Grumose degeneration” of Tretiakoff. J Neurol Sci 94: 319–323

    Google Scholar 

  3. Arai N, Yagishita S, Misugi K, Oda M, Kosaka K, Mizutani T, Morimatsu Y (1992) Peculiar axonal debris with subsequent astrocytic response (foamy spheroid body). A topographic, light microscopic, immunohistochemical and electron microscopic study. Virchows Arch [A] 420: 243–252

    Google Scholar 

  4. Arai N, Mizutani T, Morimatsu Y (1993) Foamy spheroid bodies in the globus pallidus and the substantia nigra pars reticulata: an investigation on regional distribution in 56 cases without neurodegenerative diseases. Virchows Arch [A] 422: 307–311

    Google Scholar 

  5. Barnard RO, Scott T (1980) A note on the nature of eosinophilic granular bodies in astrocytic gliomas. Acta Neuropathol (Berl) 50: 245–247

    Google Scholar 

  6. Brett M, Weller RO (1978) Intracellular serum proteins in cerebral gliomas and metastatic tumors. Neuropathol Appl Neurobiol 4: 263–272

    Google Scholar 

  7. Burger PC, Scheithauer BW, Vogel FS (1991) Surgical pathology of the nervous system and its coverings, 3rd edn. Churchill Livingstone, New York

    Google Scholar 

  8. Caine GD, Weller RO, Davis BE, Cox S (1980) Mechanisms of uptake and the fate of serum proteins and HRP in cultured human glioma cells. Acta Neuropathol (Berl) 52: 167–177

    Google Scholar 

  9. Dekker A, Krause JR (1973) Hyaline globules in human neoplasms. Arch Pathol 95: 178–181

    Google Scholar 

  10. Dickson DW, Suzuki KI, Kanner R, Weitz S, Horoupian DS (1986) Cerebral granular cell tumor: immunohistochemical and electron microscopic study. J Neuropathol Exp Neurol 45: 304–314

    Google Scholar 

  11. Doherty FJ, Osborn NU, Wassell JA, Heggie PE, Laszlo L, Mayer RJ (1989) Ubiquitin-protein conjugates accumulate in the lysosomal system of fibroblasts treated with cysteine proteinase inhibitors. Biochem J 263: 47–55

    Google Scholar 

  12. Ellis RJ, van der Vies SM (1991) Molecular chaperones. Annu Rev Biochem 60: 321–347

    Google Scholar 

  13. Galloway PG, Likavec MJ (1989) Ubiquitin in normal, reactive and neoplastic human astrocytes. Brain Res 500: 343–351

    Google Scholar 

  14. Goldman JE, Chin FC (1984) Growth kinetics, cell shape, and cytoskeleton of primary astrocyte cultures. J Neurochem 42: 175–184

    Google Scholar 

  15. Iwaki T, Fukui M, Kondo A, Takeshita I (1987) Epithelial properties of pleomorphic xanthoastrocytomas determined in ultrastructural and immunohistochemical studies. Acta Neuropathol (Berl) 74: 142–150

    Google Scholar 

  16. Iwaki T, Kume-Iwaki A, Liem RKH, Goldman JE (1989) αB-crystallin is expressed in non-Jenticular tissues and accumulations in Alexander's disease brain. Cell 57: 71–78

    Google Scholar 

  17. Iwaki T, Kume-Iwaki A, Goldman JE (1990) αB-crystallin in non-lenticular tissues. J Histochem Cytochem 38: 31–39

    Google Scholar 

  18. Iwaki T, Iwaki A, Miyazono M, Goldman JE (1991) Preferential expression of αB-crystallin in astrocytic elements of neuroectodermal tumors. Cancer 68: 2230–2240

    Google Scholar 

  19. Iwaki T, Wisniewski T, Iwaki A, Corbin E, Tomokane N, Tateishi J, Goldman JE (1992) Accumulation of αB-crystallin in central nervous system glia and neurons in pathologic conditions. Am J Pathol 140: 345–356

    Google Scholar 

  20. Iwaki T, Iwaki A, Tateishi J, Sakaki Y, Goldman JE (1993) αB-crystallin and 27-kDa heat shock protein are regulated by stress conditions in the central nervous system and accumulate in Rosenthal fibers. Am J Pathol 143: 487–495

    Google Scholar 

  21. Kawano N (1992) Pleomorphic xanthoastrocytoma: some new observations. Clin Neuropathol 11: 323–328

    Google Scholar 

  22. Kepes JJ, Rubinstein LJ, Eng LF (1979) Pleomorphic xanthoastrocytoma; a distinctive meningocerebral glioma of young subjects with relatively favorable prognosis. A study of 12 cases. Cancer 44: 1839–1852

    Google Scholar 

  23. Kepes JJ, Rubinstein LJ, Ansbacher L, Schreiber DJ (1989) Histopathological features of recurrent pleomorphic xanthoastrocytomas: further corrboration of the glial nature of this neoplasm. A study of 3 cases. Acta Neuropathol 78: 585–593

    Google Scholar 

  24. Kleihues P, Burger PC, Scheithauer BW (1993) Histological typing of tumours of the central nervous system, 2nd edn. Springer, Berlin Heidelberg New York

    Google Scholar 

  25. Kornfeldt M (1986) Granular cell glioblastoma: a malignant granular cell neoplasm of astrocytic origin. J Neuropathol Exp Neurol 45: 447–462

    Google Scholar 

  26. Kros JM, Vecht CJ, Stefanko SZ (1991) The pleomorphic xanthoastrocytoma and its differential diagnosis: a study of five cases. Hum Pathol 22: 1128–1135

    Google Scholar 

  27. Kusaka H, Hirano A, Bornstein MB, Moore GRW, Raine CS (1986) Transformation of cells of astrocyte lineage into macrophage-like cells in organotypic cultures of mouse spinal cord tissue. J Neurol Sci 72: 77–89

    Google Scholar 

  28. Lowe J, Blanchard A, Morrell K, Lennox G, Reynolds L, Billett M, Landon M, Mayer RJ (1988) Ubiquitin ia a common factor in intermediate filament inclusion bodies of diverse type in man, including those of Parkinson's disease, Pick's disease, and Alzheimer's disease, as well as Rosenthal fibres in cerebellar astrocytomas, cytoplasmic bodies in muscle, and Mallory bodies in alcoholic liver disease. J Pathol 155: 9–15

    Google Scholar 

  29. Manetto V, Abdul-Karim FW, Perry G, Tabaton M, Autilio-Gambetti L, Gambetti P (1989) Selective presence of ubiquitin in intracellular inclusions. Am J Pathol 134: 505–513

    Google Scholar 

  30. Mayer RJ, Lowe J, Landon M (1991) Ubiquitin and the lysosomal system: molecular immunopathology reveals the connection. Biomed Biochim Acta 50: 333–341

    Google Scholar 

  31. Miyazono M, Iwaki T, Kitamoto T, Shin RW, Fukui M, Tateishi J (1993) Widespread distribution of tau in the astrocytic elements of glial tumors. Acta Neuropathol 86: 236–241

    Google Scholar 

  32. Murayama S, Bouldin TW, Suzuki K (1992) Immunocytochemical and ultrastructural studies of eosinophilic granular bodies in astrocytic tumors. Acta Neuropathol 83: 408–414

    Google Scholar 

  33. Ng H-K, Lo STH (1988) Immunostaining for α1-antichymotrypsin and α1-antitrypsin in gliomas. Histopathology 13: 79–87

    Google Scholar 

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

    Google Scholar 

  35. Russell DS, Rubinstein LJ (1971) Pathology of tumours of the nervous system, 3rd edn. Arnold, London

    Google Scholar 

  36. Russell DS, Rubinstein LJ (1989) Pathology of tumours of the nervous system, 5th edn. Arnold, London

    Google Scholar 

  37. Sawa H, Takeshita I, Kuramitsu M, Mannoji H, Machi T, Fukui M, Kitamura K (1986) Neuronal and glial proteins in medulloblastomas. Immunohistochemical study. Anticancer Res 6: 905–910

    Google Scholar 

  38. Shin R-W, Ogomori K, Kitamoto T, Tateishi J (1989) Increased tau accumulation in senile plaques as a hallmark in Alzheimer's disease. Am J Pathol 134: 1365–1371

    Google Scholar 

  39. Shin RW, Iwaki T, Kitamoto T, Tateishi J (1991) Hydrated autoclave pretreatment enhances tau immunoreactivity in formalin-fixed normal and Alzheimer's disease brain tissues. Lab Invest 64: 693–702

    Google Scholar 

  40. Smith DA, Lantos PL (1985) Immunocytochemistry of cerebellar astrocytomas: with a special note on Rosenthal fibres. Acta Neuropathol 66: 155–159

    Google Scholar 

  41. Snipes GJ, Horoupian DS, Shuer LM, Silverberg GD (1992) Pleomorphic granular cell astrocytoma of the pineal gland. Cancer 70: 2159–2165

    Google Scholar 

  42. Whittle IR, Gordon A, Misra BK, Shaw JF, Steers JW (1989) Pleomorphic xanthoastrocytoma, report of four cases. J Neurosurg 70: 463–468

    Google Scholar 

  43. Yamada T, McGeer PL, McGeer EG (1992) Appearance of paired nucleated, tau-positive glia in patients with progressive supranuclear palsy brain tissue. Neurosci Lett 135: 99–102

    Google Scholar 

  44. Zorzi F, Facchetti F, Baronchelli C, Cani E (1992) Pleomorphic xanthoastrocytoma: an immunohistochemical study of 3 cases. Histopathology 20: 267–269

    Google Scholar 

  45. Zuccarello M, Sawaya R, Ray BM (1987) Immunohistochemical demonstration of alpha-1-proteinase inhibitor in brain tumors. Cancer 60: 804–809

    Google Scholar 

  46. Zülch KJ (1959) Das Glioblastom, morphologisch und biologisch gesehen. Acta Neurochir (Wien) [Suppl] 6: 2–30

    Google Scholar 

  47. Zülch KJ (1986) Brain tumours. Their biology and pathology, 3rd edn. Springer, Berlin Heidelberg New York

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hitotsumatsu, T., Iwaki, T., Fukui, M. et al. Cytoplasmic inclusions of astrocytic elements of glial tumors: special reference to round granulated body and eosinophilic hyaline droplets. Acta Neuropathol 88, 501–510 (1994). https://doi.org/10.1007/BF00296486

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00296486

Key words

Navigation