Vermian dysplasia and lipoma in a child with headache and epileptic seizure
Senay Demir, Semra Saygi
Objectives: Describing the MRI features of cerebellar dysplasia and lipoma in a child with epilepsi. Methods: A nine year old boy who has been treated for headache at our pediatric neurology dapartment had a severe seizure during his follow-up. His family descripted the seizure as 'falling on his back with unconsciousness' . The birth history was unremarkable. Family history revealed no known consanguinity. General examination revealed no dysmorphic features. Neurological examination revealed no cognitive deficits/signs to suggest cerebellar pathology. We obtained a cranial MRI which showed us that superior part of the cerebellar vermis is dysplastic and had fat signal consistant with lipoma. Results: Cerebellar malformations are a rare group of disorders with clinical heterogeneity. The congenital malformations affecting the cerebellar parenchyma are very rare. Conclusion: We describe a case of 9 years old boy with cerebellar hypoplasia accompanying a lipoma who had a severe epileptic seizure while being treated for headache, with emphasis on the MRI features of this rare entity.
Keywords: headache, epilepsi, vermian dyplasia, lipoma
Senay Demir
Baskent University Faculty of Medicine
Turkey
Semra Saygi
Baskent University Faculty of Medicine
Turkey
Objectives: Describing the MRI features of cerebellar dysplasia and lipoma in a child with epilepsi. Methods: A nine year old boy who has been treated for headache at our pediatric neurology dapartment had a severe seizure during his follow-up. His family descripted the seizure as 'falling on his back with unconsciousness' . The birth history was unremarkable. Family history revealed no known consanguinity. General examination revealed no dysmorphic features. Neurological examination revealed no cognitive deficits/signs to suggest cerebellar pathology. We obtained a cranial MRI which showed us that superior part of the cerebellar vermis is dysplastic and had fat signal consistant with lipoma. Results: Cerebellar malformations are a rare group of disorders with clinical heterogeneity. The congenital malformations affecting the cerebellar parenchyma are very rare. Conclusion: We describe a case of 9 years old boy with cerebellar hypoplasia accompanying a lipoma who had a severe epileptic seizure while being treated for headache, with emphasis on the MRI features of this rare entity.
Keywords: headache, epilepsi, vermian dyplasia, lipoma
Senay Demir
Baskent University Faculty of Medicine
Turkey
Semra Saygi
Baskent University Faculty of Medicine
Turkey
Semra Saygi
Baskent University Faculty of Medicine Turkey
Baskent University Faculty of Medicine Turkey