Giant-cell glioblastoma

Giant-cell glioblastoma
Some glioblastomas, such as this giant-cell variant, are discrete firm masses which clinically and radiographically simulate metastatic carcinoma
WHO Classification
Standard nameGiant-cell glioblastoma
StructureNeuroepithelial tumors
└►Astrocytic tumors
└►Glioblastoma
└►Giant-cell glioblastoma
ICD-O Code & WHO Grade
ICD-O Code9441/3
WHO GradeIV
Synonyms & Acronyms
SynonymsMonstrocellular sarcoma
Epidemiology
Incidence0.15/100,000/y
new cases/population/year
Age peak42
M/F ratio1.6
Prognosis
Mean overall survival12 months
Medicine WikiProject/Neurology task force

The giant-cell glioblastoma is a histological variant of glioblastoma, presenting a prevalence of bizarre, multinucleated (more than 20 nuclei) giant (up to 400 μm diameter) cells.

It occasionally shows an abundant stromal reticulin network and presents a high frequency of TP53 gene mutations.[1][2]

Symptoms and signs are similar to those of the ordinary glioblastoma. Methodology of diagnosis and treatment are the same.

Prognosis is similar to the ordinary glioblastoma (about 12 months).[3] Some authors (see later) refer cases with a slightly better outcome.

Historical annotation

The giant-cell glioblastoma was originally termed "monstrocellular sarcoma", because of its stromal reticulin network,[4][5] but the astrocytic nature of the tumor was firmly established through the consistent GFAP expression analysis.[6][7][8]

Epidemiology

Incidence

The giant-cell glioblastoma is a rare neoplasia: its incidence is less than 1% of all brain tumors. It represents up to 5% of glioblastomas.[9]

Age and sex distribution

The mean age at clinical presentation is 42. The age distribution includes children and has a wider range than other diffuse astrocytomas (diffuse WHO grade II astrocytoma, anaplastic astrocytoma, ordinary glioblastoma).[9][10][11]

The giant-cell glioblastoma affects males more frequently. (The M/F ratio is 1.6.)[1]

Prognosis

Most patients with giant-cell glioblastoma have unfavourable prognosis,[12] but some authors report clinical results slightly better than the ordinary glioblastoma,[13][14][15][16][17] in all probability because this variant seems less infiltrative, due to the nature of giant cells of this type.[1]

See also

References

  1. 1 2 3 Ohgaki H, Peraud A, Nakazato Y, Watanabe K, von Deimling A (2000). "Giant cell glioblastoma". In Kleihues P, Cavenee WK (eds.). Pathology and Genetics of Tumours of the Nervous System. Lyon: IARC. ISBN 92-832-2409-4.
  2. ↑ Macchi G. (2005) [1981]. Malattie del sistema nervoso. PICCIN Editore. ISBN 88-299-1739-7.
  3. ↑ DeAngelis LM, Loeffler JS, Adam N, Mamelak AN (2007). "Primary and Metastatic Brain Tumors". In Pazdur R, Coia LR, Hoskins WJ, Wagman LD (eds.). Cancer Management: A Multidisciplinary Approach (10th ed.). Retrieved 4 August 2009.
  4. ↑ Zulch KJ (1979). Histological Typing of Tumours of the Central Nervous System. Geneva: World Health Organization. ISBN 978-92-4-176021-8. OCLC 6845931.
  5. ↑ Zulch KJ (1986). Brain Tumors: Their Biology and Pathology (3rd ed.). Berlin Heidelberg: Springer Verlag. ISBN 978-0-387-10933-6.
  6. ↑ Jacque CM, Kujas M, Poreau A, et al. (March 1979). "GFA and S 100 protein levels as an index for malignancy in human gliomas and neurinomas". Journal of the National Cancer Institute. 62 (3): 479–83. doi:10.1093/jnci/62.3.479. ISSN 0027-8874. PMID 216839.
  7. ↑ Kleihues P, Burger PC, Scheithauer BW (1993). Histological Typing of Tumours of the Central Nervous System (2nd ed.). Berlin Heidelberg: Springer Verlag. ISBN 978-3-540-56971-8.
  8. ↑ Russell DS, Rubinstein LJ (1989). Pathology of Tumors of the Nervous System (5th ed.). London: Edward Arnold.
  9. 1 2 Palma L, Celli P, Maleci A, Di Lorenzo N, Cantore G (1989). "Malignant monstrocellular brain tumours. A study of 42 surgically treated cases". Acta Neurochirurgica. 97 (1–2): 17–25. doi:10.1007/BF01577735. ISSN 0001-6268. PMID 2718792.
  10. ↑ Meyer-Puttlitz B, Hayashi Y, Waha A, et al. (September 1997). "Molecular genetic analysis of giant-cell glioblastomas". The American Journal of Pathology. 151 (3): 853–7. ISSN 0002-9440. PMC 1857850. PMID 9284834.
  11. ↑ Peraud A, Watanabe K, Plate KH, Yonekawa Y, Kleihues P, Ohgaki H (November 1997). "p53 mutations versus EGF receptor expression in giant-cell glioblastomas". Journal of Neuropathology and Experimental Neurology. 56 (11): 1236–41. doi:10.1097/00005072-199711000-00008. ISSN 0022-3069. PMID 9370234.
  12. ↑ Huang MC, Kubo O, Tajika Y, Takakura K (April 1996). "A clinico-immunohistochemical study of giant cell glioblastoma" (Free full text). Nōshuyō Byōri. 13 (1): 11–6. ISSN 0914-8108. PMID 8916121.
  13. ↑ Margetts JC, Kalyan-Raman UP (February 1989). "Giant-celled glioblastoma of brain. A clinico-pathological and radiological study of ten cases (including immunohistochemistry and ultrastructure)" (Free full text). Cancer. 63 (3): 524–31. doi:10.1002/1097-0142(19890201)63:3<524::AID-CNCR2820630321>3.0.CO;2-D. ISSN 0008-543X. PMID 2912529.
  14. ↑ Shinojima N, Kochi M, Hamada J, et al. (August 2004). "The influence of sex and the presence of giant cells on postoperative long-term survival in adult patients with supratentorial glioblastoma multiforme". Journal of Neurosurgery. 101 (2): 219–26. doi:10.3171/jns.2004.101.2.0219. ISSN 0022-3085. PMID 15309911.
  15. ↑ Becker DP, Benyo R, Roessmann U (January 1967). "Glial origin of monstrocellular tumor. Case report of prolonged survival" (Free full text). Journal of Neurosurgery. 26 (1): 72–7. doi:10.3171/jns.1967.26.1part1.0072. ISSN 0022-3085. PMID 6018784.
  16. ↑ Burger PC, Vollmer RT (September 1980). "Histologic factors of prognostic significance in the glioblastoma multiforme" (Free full text). Cancer. 46 (5): 1179–86. doi:10.1002/1097-0142(19800901)46:5<1179::AID-CNCR2820460517>3.0.CO;2-0. ISSN 0008-543X. PMID 6260329.
  17. ↑ Klein R, Mölenkamp G, Sörensen N, Roggendorf W (June 1998). "Favorable outcome of giant cell glioblastoma in a child. Report of an 11-year survival period". Child's Nervous System. 14 (6): 288–91. doi:10.1007/s003810050228. ISSN 0256-7040. PMID 9694343.
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