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Hypertrophic olivary degeneration secondary to a Guillain Mollaret triangle cavernoma: Two case report.
Marrakchi, Salma; Hsain, Ihssan Hadj; Guelzim, Yousra; Ech-Cherif, Najwa El Kettani; Fikri, Meriem; Jiddane, Mohamed; Touarsa, Firdaous.
Afiliação
  • Marrakchi S; Neuroradiology Department, Head and Neck Hospital of Rabat, Rabat, Morocco.
  • Hsain IH; Neuroradiology Department, Head and Neck Hospital of Rabat, Rabat, Morocco.
  • Guelzim Y; Neuroradiology Department, Head and Neck Hospital of Rabat, Rabat, Morocco.
  • Ech-Cherif NEK; Neuroradiology Department, Head and Neck Hospital of Rabat, Rabat, Morocco.
  • Fikri M; Neuroradiology Department, Head and Neck Hospital of Rabat, Rabat, Morocco.
  • Jiddane M; Neuroradiology Department, Head and Neck Hospital of Rabat, Rabat, Morocco.
  • Touarsa F; Neuroradiology Department, Head and Neck Hospital of Rabat, Rabat, Morocco.
Radiol Case Rep ; 19(8): 3538-3544, 2024 Aug.
Article em En | MEDLINE | ID: mdl-38948902
ABSTRACT
Hypertrophic olivary degeneration (HOD) is a rare form of transsynaptic degeneration. It is caused by a damage at the Guillain-Mollaret triangle (GMT), which is defined by three anatomical structures the dentate nucleus, the red nucleus, and the inferior olivary nucleus (ION). Clinically, it may be revealed by palatal myoclonus. On MRI, it appears as a unilateral or bilateral enlargement of the inferior olivary nucleus which shows a high signal intensity on T2-weighted images, with sometimes a cerebellar atrophy. Here we report 2 cases of healthy patients which present hemorrhagic brainstem cavernomas, complicated later by the development of palatal myoclonus and cerebellar ataxia, with MRI features corresponding to an (HOD) secondary to a (GMT) cavernoma. The purpose is to explain the mechanism of (HOD) subsequent to lesion in (GMT), and to describe magnetic resonance imaging features.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Radiol Case Rep Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Radiol Case Rep Ano de publicação: 2024 Tipo de documento: Article