Lipoma of the corpus callosum: Case report

Mohammadine Baderddine *, El Ghabouch Mohamed, Hmamouch Mohamed Oualid, Hammoud Marouane, Lakhdar Fayçal, Benzagmout Mohamed, Chakour Khalid and Chaoui Faiz Mohamed

Department of Neurosurgery. Hassan II University Hospital Center. Fès, Morocco
 
Case Study
World Journal of Advanced Research and Reviews, 2024, 22(01), 1527–1529
Article DOI: 10.30574/wjarr.2024.22.1.1193
 
Publication history: 
Received on 11 March 2024; revised on 17 April 2024; accepted on 20 April 2024
 
Abstract: 
Corpus callosum lipoma is a very rare congenital malformation, which may be associated with varying degrees of corpus callosum dysgenesis. It is often asymptomatic but may present with epilepsy, hemiplegia, dementia, or simple headache. We report the case of a 48-year-old adult, followed for psychomotor retardation since childhood, who presented with epileptic seizures and was found to have a lipoma of the corpus callosum. Symptoms and prognosis depend on the associated malformation. MRI is the imaging modality of choice for diagnosis. Treatment is symptomatic: antiepileptic drugs in the event of epileptic seizures, and surgery is rarely indicated.
 
Keywords: 
Lipoma; Corpus callosum; Seizures; MRI.
 
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