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Pericallosal lipoma: A case report.
Nasri, Siham; Aggari, Hanane El; Afilal, Ihssane; Aichouni, Narjiss; Kamaoui, Imane; Skiker, Imane.
Afiliação
  • Nasri S; Department of Radiology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed First, Oujda, Morocco.
  • Aggari HE; Department of Radiology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed First, Oujda, Morocco.
  • Afilal I; Department of Radiology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed First, Oujda, Morocco.
  • Aichouni N; Department of Radiology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed First, Oujda, Morocco.
  • Kamaoui I; Department of Radiology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed First, Oujda, Morocco.
  • Skiker I; Department of Radiology, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, University Mohammed First, Oujda, Morocco.
Radiol Case Rep ; 17(9): 3094-3096, 2022 Sep.
Article em En | MEDLINE | ID: mdl-35789560
ABSTRACT
Pericallosal lipoma or lipoma of the corpus callosum is a rare congenital brain malformation that can be associated to dysgenesis or agenesis of the corpus callosum. It is usually asymptomatic, but can be revealed by epilepsy, paresis, paralysis, dementia, or headaches. CT and MR imaging play an important role in making this diagnosis. Lipoma of the corpus callosum can present as 2 different types tubulonodular and curvilinear. Tubulonodular lipomas are the most common morphology. We report a case of 60-year-old woman, admitted for a seizure following a head trauma that benefited from a head CT revealing a curvilinear lipoma of the Corpus Callosum.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Radiol Case Rep Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Radiol Case Rep Ano de publicação: 2022 Tipo de documento: Article