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Pathology of meningiomas

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Abstract

Because meningiomas arise from arachnoid cells present in the meninges, they can occur in any location where meninges or ectopic meninges exist, such as the nasal cavity, the paranasal sinuses, the middle ear, and even the mediastinum. Although the tumors may range in appearance from epithelial to mesenchymal, they are characterized by a uniform distribution of cells with shapes ranging from polygonal epithelial-like to spindled and fusiform. Historically, classification of meningiomas has been based upon cell shapes, cell patterns, cell products, or stroma, implying clinicopathologic differences among the types. Numerous observations have shown that certain conditions may indicate a predisposition for developing meningiomas, prompting extensive studies of meningiomas using cytogenetic techniques. Meningiomas are common neoplasms arising from the central nervous system meninges. They are important because of the morbidity they produce. Their critical intracranial and intraspinal locations make diagnosis and surgical removal difficult.

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References

  1. Cushing H: The meningiomas (dural endotheliomas). Their source and favoured seats of origin. (Cavendish lecture) Brain 45: 282–316, 1922

    Google Scholar 

  2. Kepes JJ: Meningiomas: Biology, Pathology, Differential Diagnosis. Masson, New York, 1982

    Google Scholar 

  3. Longstreth WT, Dennis LK, McGuire VM, et al.: Epidemiology of intracranial meningioma. Cancer 72: 639–648, 1993

    Google Scholar 

  4. Rohringer M, Sutherland GR, Louw DF, Sima AAF: Incidence and clinicopathological features of meningioma. J Neurosurgery 71: 665–72, 1989

    Google Scholar 

  5. Kleihues P, Burger PC, Scheithauer BW: Histological Typing of Tumours of the Central Nervous System. Berlin: Springer, 1993 (WHO International Histological Classification of Tumours), pp 33–37

    Google Scholar 

  6. Jellinger K, Slowik F: Histological subtypes and prognostic problems in meningiomas. J Neurol 208: 279–298, 1975

    Google Scholar 

  7. Ng HK: Atypical and malignant meningioma: Any easy diagnostic criteria? Advances in Anat Pathol 1: 44–48, 1994

    Google Scholar 

  8. Maier H, Öfner D, Hittmair A, Kitz K, Budka H: Classic, atypical, and anaplastic meningioma: three histopathological subtypes of clinical relevance. J Neurosurg 77: 616–623, 1992

    Google Scholar 

  9. Langford LA, Cooksley CS, DeMonte F: Comparison of MIB-1 (Ki-67 antigen) and BUdR proliferation indices in meningiomas. Hum Patho1, 1995 (in press)

  10. Martuza RL, Eldridge R: Neurofibromatosis 2 (Bilateral acoustic neurofibromatosis). New Engl J Med 318: 684–688, 1988

    Google Scholar 

  11. Wertelecki W, Rouleau GA, Superneau DW et al.: Neurofibromatosis 2: Clinical and DNA linkage studies of a large kindred. New Engl J Med 319: 278–283, 1988

    Google Scholar 

  12. Seizinger BR, de al Monte S, Atkins L, et al.: Molecular genetic approach to human meningioma: loss of genes on chromosome 22. Proc Natl Acad Sci USA 84: 5419–5423, 1987

    Google Scholar 

  13. Collins VP, Nordenskjöld M, Dumanski JP: The molecular genetics of meningiomas. Brain Pathology 1: 19–24, 1990

    Google Scholar 

  14. Dumanski JP, Carlborn E, Collins VP, Nerdenskjöld M: Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma. Proc Natl Acad Sci USA 84: 9275–9279, 1987

    Google Scholar 

  15. Pulst SM, Rouleau GA, Marineau C, Fain P, Sieb JP: Familial meningioma is not allelic to neurofibromatosis 2. Neurology 43: 2096–2098, 1993

    Google Scholar 

  16. Trofatter JA, MacCollin MM, Rutter JL, et al.: A novel moiesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor. Cell 72: 791–800, 1993

    Google Scholar 

  17. Wolff RK, Frazer KA, Jackler RK, et al.: Analysis of chromosome 22 deletions in neurofibromatosis type 2-related tumors. Am J Hum Genet 51: 478–485, 1992

    Google Scholar 

  18. Rouleau GA, Merel P, Lutchman M et al.: Alteration in a new gene encoding a putative membrane-organizing protein causes neurofibromatosis type 2. Nature 363: 515–521, 1993

    Google Scholar 

  19. Sanson M, Marineau C, Desmaze C, et al.: Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus. Hum Mol Genet (England) 2: 1215–1220, 1993

    Google Scholar 

  20. Ruttledge MH, Sarrazin J, Rangaratnam S, et al.: Evidence for the complete inactivation of the NF2 gene in the majority ] of sporadic meningiomas. Nature Genetics 6: 180–183, 1994

    Google Scholar 

  21. Ruttledge MH, Xie Y-G, Han F-Y, et al.: Deletions on chromosome 22 in sporadic meningioma. Genes, Chromosomes & Cancer 10: 122–130, 1994

    Google Scholar 

  22. Ron E, Modan B, Boice JD, et al.: Tumors of the brain and nervous system after radiotherapy in childhood. N Engl J Med 319: 1033–1039, 1988

    Google Scholar 

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Langford, L.A. Pathology of meningiomas. J Neuro-Oncol 29, 217–221 (1996). https://doi.org/10.1007/BF00165651

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  • DOI: https://doi.org/10.1007/BF00165651

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