Skip to main content
Log in

Hippocampal neuronal density in temporal lobe epilepsy with and without gliomas

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

Summary

The majority of patients with temporal lobe epilepsy show hippocampal sclerosis, which pathologically represents neuronal loss and gliosis. We studied volumetric neuronal density on a representative mid to mid-posterior level slice of hippocampi surgically removed from intractable temporal lobe epilepsy cases, and compared the results between 25 non-tumor epilepsy (NTE) cases and 5 tumor-associated epilepsy (TAE) cases. Eleven age-matched non-epileptic autopsy cases were studied as controls. Cells were counted in the CA1 through CA4 fields and the stratum granulosum of the dentate fascia. In NTE every hippocampal field showed statistically significant loss of neurons, the neuronal density in each field ranging from 35% to 50% of that of control. The mean neuronal density between the TAE and NTE groups also showed statistically significant differences in all hippocampal fields. The neuronal density of hippocampal fields of NTE ranged from 43% to 58% of that of TAE. Tumor-associated epilepsy cases, however, failed to show any statistically significant deviation from the control in their neuronal density. The etiology of the difference in neuronal density between the TAE and NTE groups is discussed.

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. Abercrombie M (1946) Estimation of nuclear population from microtome section. Anat Rec 94:239–247

    Google Scholar 

  2. Adams CBT, Anslow P, Molyneux A, Oxbury J (1987) Radiological detection of surgically treatable pathology. In: Engel J Jr (ed) Surgical treatment of the epilepsies. Raven Press, New York, pp 213–233

    Google Scholar 

  3. Babb TL, Lieb JP, Brown WJ, Pretorius J, Crandall PH (1984) Distribution of pyramidal cell density and hyperexcitability in the epileptic human hippocampal formation. Epilepsia 25: 721–728

    Google Scholar 

  4. Babb TL, Brown WJ, Pretorius J, Davenport C, Lieb JP, Crandall PH (1984) Temporal lobe volumetric cell densities in temporal lobe epilepsy. Epilepsia 25:729–740

    Google Scholar 

  5. Baab TL, Brown WJ (1987) Pathological findings in epilepsy. In: Engel J Jr (ed) Surgical treatment of the epilepsies. Raven Press, New York, pp 511–540

    Google Scholar 

  6. Brown WJ, Babb TL (1987) Neuropathological changes in the temporal lobe associated with complex partial seizures. In: Hopkins A (ed) Epilepsy. Chapman & Hall, London, pp 300–416

    Google Scholar 

  7. Bruton CJ (1988) The neuropathology of temporal lobe epilepsy. Oxford University Press, London, pp 61–69

    Google Scholar 

  8. Cavanagh JB, Meyer A (1956) Aetiological aspects of Ammon's horn sclerosis associated with temporal lobe epilepsy. Br Med 12:1403–1407

    Google Scholar 

  9. Cavanagh JB (1958) On certain small tumours encountered in the temporal lobe. Brain 81:389–405

    Google Scholar 

  10. Currie S, Heatherfield KWG, Henson RA, Scott DF (1971) Clinical course and prognosis of temporal lobe epilepsy. A survey of 666 patients. Brain 94:173–190

    Google Scholar 

  11. Earle KM, Baldwin M, Penfield W (1953) Incisural sclerosis and temporal lobe seizures produced by hippocampal herniation at birth. Arch Neurol Psychiatry 69:27–42

    Google Scholar 

  12. Flaconer MA, Serafetinides EA (1963) A follow-up study of surgery in temporal lobe epilepsy. J Neurol Neurosurg Psychiatry 26:154–165

    Google Scholar 

  13. Falconer MA, Serafetinides EA, Corsellis JAN (1964) Etiology and pathogenesis of temporal lobe epilepsy. Arch Neurol 10:233–248

    Google Scholar 

  14. Falconer MA (1974) Mesial temporal (Ammon's horn) sclerosis as a common cause of epilepsy. Aetiology, treatment, and prevention. Lancet II:767–770

    Google Scholar 

  15. Gastaut H, Gastaut JL (1976) Computerized transverse axial tomography in epilepsy. Epilepsia 17:325–336

    Google Scholar 

  16. Gastaut H, Toga M, Roger J, Gibson WC (1959) A correlation of clinical electroencephalographic and anatomical findings in nine autopsied cases of “temporal lobe epilepsy”. Epilepsia 1:56–85

    Google Scholar 

  17. Griffiths T, Evans MC, Meldrum BS (1983) Intracellular calcium accumulation in rat hippocampus during seizures induced by bicuculline or l-allyglycine. Neuroscience 10:385–395

    Google Scholar 

  18. Jensen I, Klinken L (1976) Temporal lobe epilepsy and neuropathology. Acta Neurol Scand 54:391–414

    Google Scholar 

  19. Ketz E (1974) Brain tumors and epilepsy. Hndb Clin Neurol 16:254–269

    Google Scholar 

  20. Kim JH, Guimaraes PO, Shen MY, Deutch C, Spencer SS, Spencer DD (1988) Hippocampal volumetric neuronal density in temporal lobe epilepsy. Soc Neurosci Abstr 14:1032

    Google Scholar 

  21. King DW, Flanigin HF, Gallagher BB, So EL, Murvin AJ, Smith DB, Oommen KJ, Feldman DS, Power J (1986) Temporal lobectomy for partial complex seizures: Evaluation, results, and 1-year follow-up. Neurology 36:334–339

    Google Scholar 

  22. Kuzniecky R, De la Sayette V, Ethier R, Melanson D, Andermann F, Berkovic S, Robitaille Y, Olivier A, Peters T, Feindel W (1987) Magnetic resonance imaging in temporal lobe epilepsy: pathological correlations. Ann Neurol 22:341–347

    Google Scholar 

  23. Laws ER, Taylor WF, Clifton MB, Okazaki H (1984) Neurosurgical management of low-grade astrocytoma of the cerebral hemispheres. J Neurosurg 61:665–673

    Google Scholar 

  24. Lorente de Nó R (1934) Studies on the structure of the cerebral cortex. II. J Psychol Neurol 46:113–177

    Google Scholar 

  25. Margerison JH, Corsellis JAN (1966) Epilepsy and the temporal lobes. Brain 89:499–529

    Google Scholar 

  26. McKeran RO, Thomas DGT (1980) The clinical study of gliomas. In: Thomas DGT, Graham DI (eds) Brain tumors. Scientific basis, clinical investigation and current therapy. Butterworths, London, pp 194–230

    Google Scholar 

  27. Mouritzen Dam A (1979) The density of neurons in human hippocampus. Neuropathol Appl Neurobiol 5:249–264

    Google Scholar 

  28. Mouritzen Dam A (1980) Epilepsy and neuron loss in the hippocampus. Epilepsia 21:617–629

    Google Scholar 

  29. Olney JW (1978) Neurotoxicity of excitatory amino acids. In: McGreer E, Onley JW, McGreer P (eds) Kainic acid as a tool in neurobiology. Raven Press, New York, pp 95–121

    Google Scholar 

  30. Rasmussen TB (1983) Surgical treatment of complex partial seizures: results, lessons, and problems. Epilepsia 24 [Suppl 1]:S65-S76

    Google Scholar 

  31. Rich KM, Goldring S, Gado M (1985) Computed tomography in chronic seizure disorder caused by glioma. Arch Neurol 42:26–27

    Google Scholar 

  32. Sager HJ, Oxburg JM (1987) Hippocampal neuron loss in temporal lobe epilepsy: correlation with early childhood convulsions. Ann Neurol 2:334–340

    Google Scholar 

  33. Sano K, Malamud N (1953) Clinical significance of sclerosis of the cornu ammonis. Arch Neurol Psychiatry 70:40–53

    Google Scholar 

  34. Scott GM, Gibberd FB (1980) Epilepsy and other factors in the prognosis of gliomas. Acta Neurol Scand 61:227–239

    Google Scholar 

  35. Scholz W (1933) Über die Entstehung des Hirnbefundes bei der Epilepsie. Z Gesamte Neurol Psychiatr 145:471–515

    Google Scholar 

  36. Scholz W (1959) The contribution of patho-anatomical research to the problem of epilepsy. Epilepsia 1:36–55

    Google Scholar 

  37. Sommer W (1880) Erkrankungen des Ammonshorns als aetiologisches Moment der Epilepsie. Arch Psychiatr Nervenkr 10: 631–675

    Google Scholar 

  38. Spencer DD, Spencer SS, Mattson RH, WIlliamson PD (1984) Intracerebral masses in patients with intractable partial epilepsy. Neurology 34:432–436

    Google Scholar 

  39. Spencer DD, Spencer SS, Mattson RH, Williamson PD, Novelly RA (1984) Access to the posterior medial temporal lobe structures in the surgical treatment of temporal lobe epilepsy. Neurosurgery 15:667–671

    Google Scholar 

  40. Spencer DD (1987) Postscript: should there be a surgical treatment of choice, and if so, how should it be determined? In: Engel J Jr (ed) Surgical treatment of the epilepsies. Raven Press, New York, pp 477–484

    Google Scholar 

  41. Spencer SS, Spencer DD, Kim JH, Glaser GS (1987) Gliomas in chronic epilepsy. In: Wolf P, Dam M, Dreifuss DJ (eds) Advances in epileptology, vol 16. Raven Press, New York, pp 39–41

    Google Scholar 

  42. Spielmeyer W (1930) The anatomic substratum of the convulsive state. Arch Neurol Psychiatry 23:869–875

    Google Scholar 

  43. Wilden JN, Kelly PJ (1987) CT computerized sterotactic biopsy for low density CT lesions presenting with epilepsy. J Neurol Neurosurg Psychiatry 50:1302–1305

    Google Scholar 

  44. Williams PL, Warwick R (1975) Functional neuroanatomy of man. WB Saunders Co, Philadelphia, pp 938–941

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Supported by NIH grant NS06208

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kim, J.H., Guimaraes, P.O., Shen, M.Y. et al. Hippocampal neuronal density in temporal lobe epilepsy with and without gliomas. Acta Neuropathol 80, 41–45 (1990). https://doi.org/10.1007/BF00294220

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00294220

Key words

Navigation