Skip to main content
Log in

Surgical therapy of lesions within the hypothalamic region

  • Published:
Acta Neurochirurgica Aims and scope Submit manuscript

Summary

On one hand pituitary microadenomas with autonomous character and those, which had been influenced by hypothalamic disorders, are summarized and discussed. On the other hand, the neurosurgical management of tumours, adjacent to or involved with the hypothalamus, are described.

Endocrinologically active pituitary adenomas are characterized by their hormone excess of ACTH, GH, and prolactin. In Cushing's disease endocrine and clinical remission occurred in 74%. 3 patients out of this group showed a reincrease of ACTH after a period of remission, indicating a possible hypothalamic influence. In acromegaly the hypothalamic influence is also discussed. One patient with an ectopic GRF-producing tumour showing a reincrease of GH levels after successful transsphenoidal adenomectomy has been described. In microprolactinomas, 7 patients out of 45 showed a reincrease of prolactin-levels after a period of normalization, we also discussed hypothalamic disorders.

Tumours with suprasellar extension such as macroadenomas without endocrine activity and meningiomas are removed nowadays with minimal risk for the life of the patients. In craniopharyngiomas radical excision is accompanied by a high risk of hypothalamic defects caused by mechanical lesions and possible secondary vasospasm.

Finally the excision of a hamartoma growing from the floor of the third ventricle into the interpeduncular cistern is discussed. Up to now the successful excision could be documented by endocrinological data, which give no sign of further growth of the hamartoma.

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.

Institutional subscriptions

Similar content being viewed by others

References

  1. Carmel, P. W., Surgical syndromes of the hypothalamus. In: Clinical neurosurgery, pp. 133–159. Baltimore-London: Williams and Wilkins. 1980.

    Google Scholar 

  2. Carmel, P. W., Tumours of the third ventricle. Acta Neurochir. (Wien) (1985). (This volume.)

  3. Faglia, G., Paracchi, A., Ferrari, C., Beck-Peccoz, P., Evaluation of the results of transsphenoidal surgery in acromegaly by assessment of the growth hormone response to thyreotropinreleasing hormone. Clin. Endocrinol. (Oxf.)8 (1978), 373–380.

    Google Scholar 

  4. Faglia, G., Moriondo, P., Travaglin, P., Giovanelli, M. A., Influence of previous bromocriptin therapy on surgery for microprolactinomas. LancetI (1983), 133–134.

    Google Scholar 

  5. Fahlbusch, R., Müller, O. A., Werder, K. von, Endocrinological disturbances in parasellar processes. Acta Neurochir. (Wien) Suppl.28 (1978), 456–460.

    Google Scholar 

  6. Fahlbusch, R., Müller, O. A., Werder, K. von, Perioperative ACTH, GH and PRL levels in patients with Cushing's disease, acromegaly and hyperprolactinemia. Acta endocrin. (Kbh.), Suppl.225 (1979), 202.

    Google Scholar 

  7. Fahlbusch, R., Surgical treatment of pituitary adenoma. In: The pituitary (Beardwell, C., Robertson, G. I., eds.), PP. 76–105. London-Boston-Sydney-Wellington-Durban-Toronto: Butter-worths. 1981.

    Google Scholar 

  8. Fahlbusch, R., Marguth, F., Optic nerve compression by pituitary adenomas. In: The cranial nerves (Samii, M., Jannetta, P. J., eds.), pp. 140–147. Berlin-Heidelberg-New York: Springer. 1981.

    Google Scholar 

  9. Fahlbusch, R., Marguth, F., Tumoren der Hypophyse. Klinische Neurochirurgie, Vol. II (Dietz, H., Umbach, W., Wüllenweber, R., eds.), pp. 86–106. Stuttgart-New York: Thieme. 1984.

    Google Scholar 

  10. Fahlbusch, R., Buchfelder, M., Werder, K. von, Present status of surgical treatment of prolactinomas: a long-term follow-up III. European Workshop of pituitary adenomas (in press). 1984 a.

  11. Fahlbusch, R., Murr, R., Enzenbach, R., Postoperative Komplikationen in der Neurochirurgie. In: Organversagen während Intensivtherapie (Peter, K., Lavin, P., Jesch, F., eds.). Stuttgart-New York: Thieme. 1984 b.

    Google Scholar 

  12. Fröhlich, A., Ein Fall von Tumor der Hypophysis cerebri ohne Akromegalie. Wien. Klin. Rundschau15 (1901), 883–906.

    Google Scholar 

  13. Hadjilambris, K., Fahlbusch, R., Heinze, E., True precocious puberty of a girl with hamartoma of the CNS successfully operated Eur. J. Pediatr. 1985 (accepted).

  14. Haymaker, W., Blood supply of the human hypothalamus. In: The hypothalamus (Haymaker, W., Anderson, E., Nauta, W. J. H., eds.), pp. 210–218. Springfield, III.: Ch.C Thomas. 1969.

    Google Scholar 

  15. Kobayashi, N., Kageyama, N., Ohara, K., Internal irradiation for cystic craniopharyngioma. J. Neurosurg.55 (1981), 896–903.

    PubMed  Google Scholar 

  16. Lang, J., Surgical anatomy of the hypothalamus. (This volume.)

  17. Müller, O. A., Fahlbusch, R., Differential therapy in patients with Cushing's disease. Acta endocr. (Kbh.), Suppl.215 (1978), 23.

    Google Scholar 

  18. Müller, O. A., ACTH im Plasma: Bestimmungsmethoden und klinische Bedeutung. Stuttgart: Thieme-Copythek. 1980.

    Google Scholar 

  19. Müller, O. A., Stalla, G. K., Werder, K. von, Corticotropin releasing factor: A new tool for the differential diagnosis of Cushing's syndrome. J. Clin. Endocrinol. Metab.57 (1983), 227–229.

    PubMed  Google Scholar 

  20. Müller, O. A., Stalla, G. K., Hartwimmer, J., Schopohl, J., Werder, K. von, Corticotropin releasing factor (CRF): Diagnostic implications. (This volume.)

  21. Orth, D. N., Liddle, G. W., Results of treatment in 108 patients with Cushing's syndrome. N. Engl. J. Med.285 (1971), 534–542.

    PubMed  Google Scholar 

  22. Orth, D. N., de Bold, C. R., de Cherney, G. S., Pituitary microadenomas causing Cushing's disease respond to corticotropin-releasing factor. J. Clin. Endocrinol. Metab.55 (1982), 1017–1019.

    PubMed  Google Scholar 

  23. Orth, D. N., The old and the new in Cushing's syndrome. N. Engl. J. Med.310 (1984), 649–651.

    PubMed  Google Scholar 

  24. Plum, F., van Uitert, R., Nonendocrine diseases and disorders of the hypothalamus. In: The hypothalamus (Reichlin, S., ed.), pp. 415–473. New York: Raven Press. 1978.

    Google Scholar 

  25. Quabbe, A. J., Endocrinology of growth hormone producing tumours. In: Treatment of pituitary adenomas (Fahlbusch, R., Werder, K. von, eds.), pp. 47–60. Stuttgart, PSG Massachussetts: Thieme. 1978.

    Google Scholar 

  26. Quabbe, A. J., Treatment of acromegaly by transsphenoidal operation 90-yttrium implantation and bromocriptin: results in 230 patients. Clin. endocrinol.16 (1982), 107–119.

    Google Scholar 

  27. Quabbe, A. J., Hypothalamic control of GH secretion. (This volume.)

  28. Reichlin, S., Overview of the anatomical and physiologic basis of anterior pituitary regulation. Clin. Neuroendocrinol. (1979), 1–13.

  29. Serri, O., Rasio, E., Beauregard, H., Hardy, J., Somma, M., Recurrence of hyperprolactinemia after selective transsphenoidal adenomectomy in women with prolactinoma. N. Engl. J. Med.309 (1983), 280–283.

    PubMed  Google Scholar 

  30. Solero, C. L., Giombini, S., Morello, G., Suprasellar and olfactory meningiomas. Report on a series of 153 personal cases. Acta Neurochir. (Wien)67 (1983), 181–194.

    Google Scholar 

  31. Sung, D. J., Chung, Ch. H., Harisiadis, C., Carmel, P., Treatment results of craniopharyngiomas. Cancer (Philad.)47 (1981), 847–852.

    Google Scholar 

  32. Sturm, V., Rommel, Th., Strauss, L., Georgi, P., Scherer, K. E., Steude, U., Stock, G., Penzholz, H., Backlund, E. O., Preliminary results of intracavitary irridation of cystic craniopharyngiomas by means of stereotactically applied yttrium-90. In: Advances in neurosurgery, Bd. IX (Schiefer, W., Klinger, M., Brock, M., eds.), pp. 401–404. Berlin-Heidelberg-New York: Springer. 1981.

    Google Scholar 

  33. Symon, L., Logue, V., Jakubowski, J., The surgical treatment of craniopharyngioma. In: Modern neurosurgery (Brock, M., ed.), pp. 187–192. Berlin-Heidelberg-New York: Springer. 1982.

    Google Scholar 

  34. Takeuchi, J., Handa, H., Miki, Y., Munemitsu, H., Aso, T., Precocious puberty due to a hypothalamic hamartoma. Surg. Neurol.11 (1979), 456–460.

    PubMed  Google Scholar 

  35. Thorner, M. D., Perryman, L., Cronin, M. J., Rogal, A. D., Draznin, M., Johanson, A., Vale, W., Horvath, E., Kovacs, K., Somatotroph hyperplasia. Sucessful treatment of acromegaly by removal of a pancreatic islet tumor secreting a growth hormonereleasing factor. J. Clin. Invest.70 (1982), 965–977.

    PubMed  Google Scholar 

  36. Thorner, M. O.,et al, Human pancreatic tumor GH-reieasing factor. (This volume.)

  37. Visot, A., Rougerie, J., Derome, J., Evrard, E., Gliomes optochiasmatiques. Neurochirurgie26 (1980), 181–192.

    PubMed  Google Scholar 

  38. Werder, K. von, Losa, M., Stalla, G. K., Pak, L., Müller, O. A., Tumour pancreatic growth hormone releasing factor (hp GRF): GRF and GH levels after injection and infusion of hp GRF1–44. (This volume.)

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Fahlbusch, R., Schrell, U. Surgical therapy of lesions within the hypothalamic region. Acta neurochir 75, 125–135 (1985). https://doi.org/10.1007/BF01406333

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01406333

Keywords

Navigation