Skip to main content
Log in

Cavernomas of the central nervous system: Clinical syndromes, CT scan diagnosis, and prognosis after surgical treatment in 25 cases

  • Published:
Acta Neurochirurgica Aims and scope Submit manuscript

Summary

We present our clinical experience and the results of surgical management with 25 cavernomas of the CNS, treated in our hospital in the last 10 years. The location of the lesion assessed by clinical and CT scan examinations, proved to be the most significative factor determining the prognosis of cavernomas of the CNS, after surgical removal.

The symptoms started in most of the cases in the third decade of life. 19 cases were located in the cerebral hemispheres and produced three well defined clinical syndromes:

  1. 1)

    Irritative syndrome (seizures) present in 70% of the cases.

  2. 2)

    Space-occupying lesion syndrome (20%) and

  3. 3)

    haemorrhagic syndrome (10%).

The remaining six cases were located within the basal ganglia, brainstem, pineal region, cerebellum and spinal cord, showing a progressive course.

CT scan studies were performed on 24 cases. The characteristic image of a cavernoma is represented by a moderately hyperdense nodule with discreet contrast uptake. Calcification was observed in and around the lesions in 33% of the cases. Perilesional hypodensities suggestive of brain tissue atrophy were noted in 22% of the CT scans. On the other hand, 12% of cerebral hemisphere cavernomas showed atypical CT scan images that suggested an erroneous diagnosis of cystic gliomas.

Radical surgical removal was performed in all cases. The postoperative results varied according to the location of the lesions. Complete recovery was obtained with cerebral hemisphere cavernomas presenting with a progressive history suggesting tumour or a haemorrhagic syndrome. 85% of the cases presenting with seizures, were symptom-free and taking no anticonvulsants 1 year after surgery. In deeply placed cavernomas (basal ganglia and brainstem) the surgical results were poor. In the latter cases surgery has to be carefully evaluated when a mode of treatment is to be considered in patients whose CT scan data strongly suggest a diagnosis of cavernoma.

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. Bartlett JE, Kishore PRS (1977) Intracranial cavernous angioma. Am J Roentgenol 128: 653–656

    Google Scholar 

  2. Crawford JV, Russell DS (1956) Cryptic arteriovenous and venous hamartomas of the brain. J Neurol Neurosurg Psychiatry 19: 1–11

    Google Scholar 

  3. Giombini S, Morello G (1978) Cavernous angiomas of the brain. Account of fourteen personal cases and review of the literature. Acta Neurochir (Wien) 40: 61–82

    Google Scholar 

  4. Golden JB, Kramer RA (1978) The angiographically occult cerebrovascular malformation. Report of three cases. J Neurosurg 48: 292–296

    PubMed  Google Scholar 

  5. Khosla VK, Banerjee AK, Mathuriya SN, Mehta S (1984) Giant cystic cavernoma in a child. Case report. J Neurosurg 60: 1297–1299

    PubMed  Google Scholar 

  6. Kramer RA, Wing SD (1977) Computed tomography of angiographically occult cerebral vascular malformations. Radiology 123: 649–652

    PubMed  Google Scholar 

  7. Pozzati E, Padovani R, Morrone B, Finizio F, Gaist G (1980) Cerebral cavernous angiomas in children. J Neurosurg 53: 826–832

    PubMed  Google Scholar 

  8. Ramina R, Ingunza W, Vonofakos D (1980) Cystic cerebral cavernous angioma with dense calcification. Case report. J Neurosurg 52: 259–262

    PubMed  Google Scholar 

  9. Russell DS, Rubinstein LJ (1977) Pathology of tumours of the nervous system, ed 4. Williams and Wilkins, Baltimore, pp 127–141

    Google Scholar 

  10. Terao H, Hori T, Matsutani M, Okeda R (1979) Detection of cryptic vascular malformations by computerized tomography. Report of two cases. J Neurosurg 51: 546–551

    PubMed  Google Scholar 

  11. Vaquero J, Carrillo R, Cabezudo J, Leunda G, Villoria F, Bravo G (1980) Cavernous angiomas of the pineal region. Report of two cases. J Neurosurg 53: 833–835

    PubMed  Google Scholar 

  12. Vaquero J, Cabezudo JM, Leunda G (1983) Cystic cavernous haemangiomas of the brain. Acta Neurochir (Wien) 67: 135–138

    Google Scholar 

  13. Vaquero J, Leunda G, Martinez R, Bravo G (1983) Cavernomas of the brain. Neurosurgery 12: 208–210

    PubMed  Google Scholar 

  14. Voigt K, Yaşargil MG (1976) Cerebral cavernous haemangiomas or cavernomas: Incidence, pathology, localization, diagnosis, clinical features and treatment. Review of the literature and report of an unusual case. Neurochirurgia (Stuttgart) 19: 59–68

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Vaquero, J., Salazar, J., Martínez, R. et al. Cavernomas of the central nervous system: Clinical syndromes, CT scan diagnosis, and prognosis after surgical treatment in 25 cases. Acta neurochir 85, 29–33 (1987). https://doi.org/10.1007/BF01402366

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01402366

Keywords

Navigation