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Review
. 2010 Dec;26(12):1819-23.
doi: 10.1007/s00381-010-1237-4. Epub 2010 Jul 28.

A peri-trigonal giant tumefactive cavernous malformation: case report and review of literature

Affiliations
Review

A peri-trigonal giant tumefactive cavernous malformation: case report and review of literature

Sumit Thakar et al. Childs Nerv Syst. 2010 Dec.

Abstract

Introduction: Giant cavernous malformations (GCMs) constitute an uncommon entity in the diagnostic armamentarium of the neurosurgeon. We report a 3-year-old boy with a GCM in the peri-trigonal region and review 13 other paediatric cases previously reported in literature.

Case: A 3-year-old boy presented with right-sided hemiparesis and features of raised intracranial pressure of short duration. Computed tomography showed a large left peri-trigonal mass with a bleed. Magnetic resonance imaging showed associated perilesional edema and mass effect, rendering the lesion a tumefactive appearance. He underwent total excision of the lesion, with subsequent recovery of hemiparesis. Histopathology was reported as a cavernoma.

Discussion: The clinico-radiological presentation of GCM is discussed based on a case report and relevant cases in literature. Good surgical outcome can be expected with total microsurgical excision.

Conclusion: A giant cavernous malformation should be one of the differentials of a lesion with a tumefactive clinico-radiological presentation in children. There should be a high index of suspicion for such a diagnosis, especially when the lesion does not enhance with contrast. This is the third case report in paediatric literature describing a periventricular location of this unusual lesion.

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References

    1. Childs Nerv Syst. 1985;1(4):230-3 - PubMed
    1. Surg Neurol. 1997 Dec;48(6):610-4 - PubMed
    1. Neurosurgery. 2004 Oct;55(4):979-80 - PubMed
    1. J Neurosurg. 1998 Sep;89(3):465-9 - PubMed
    1. Arch Neurol Psychiatry. 1948 Jul;60(1):20-36 - PubMed

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