Publications of Bernard OTTO
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See detailLa prise en charge des anévrismes intracrâniens non rompus
Martin, Didier ULiege; OTTO, Bernard ULiege; DARSAUT, Tim et al

in Revue Médicale de Liège (2018), 73

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See detailL'image du mois. L'encéphalopathie postérieure réversible.
COUSIN, François ULiege; JEDIDI, Zayd ULiege; OTTO, Bernard ULiege et al

in Revue Médicale de Liège (2016), 71(11)

Nous rapportons ici le cas d'une patiente de 32 ans, sans antécédents, ayant présenté une encéphalopathie postérieure réversible toxique sur prise d'Antabuse.

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See detailL'écho-doppler transcrânien dans la prise en charge des sténoses artérielles cervicales et intracrâniennes
SCHOYSMAN, Laurent ULiege; TSHIBANDA, Luaba ULiege; OTTO, Bernard ULiege et al

in Revue Médicale de Liège (2014), 69

Le progrès technique en imagerie a permis le développement de l’écho-Doppler transcrânien en mode duplex ou triplex. A côté des autres techniques de neuro-imagerie, son intérêt dans la pathologie ... [more ▼]

Le progrès technique en imagerie a permis le développement de l’écho-Doppler transcrânien en mode duplex ou triplex. A côté des autres techniques de neuro-imagerie, son intérêt dans la pathologie vasculaire cérébrale va grandissant. Le présent article a pour but de présenter cette technique en détaillant ses indications actuelles chez les patients présentant des sténoses artérielles cervicales et intra-crâniennes. [less ▲]

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See detailLes paralysies du nerf moteur oculaire commun chez l'enfant: a propos d'une observation de tumeur germinale hypophysaire.
Kalenga, Mbu; COLLIGNON, Nathalie ULiege; ANDRIS, Cécile ULiege et al

in Bulletin de la Société Belge d'Ophtalmologie (2011), (318), 31-6

PURPOSE: Third cranial nerve palsies are unfrequent in childhood and adolescence and are most often congenital. The association of sellar germ cell tumor and ophthalmoplegia is considered as being very ... [more ▼]

PURPOSE: Third cranial nerve palsies are unfrequent in childhood and adolescence and are most often congenital. The association of sellar germ cell tumor and ophthalmoplegia is considered as being very rare at this age. CASE REPORT: A 11-year-old young girl was examined in emergency with a third left cranial nerve partial palsy associated with one- year duration history of hypopituitarism with insipid diabetes and growth retardation. Cerebral IRM revealed a tumor of the pituitary gland. In histopathological examination of pituitary gland biopsies, lesions were compatibles with a sellar germ cell tumor. CONCLUSION: Although they are most often of a congenital nature, third cranial nerve palsies in childhood may be secondary to other causes that should be always taken in mind. When they are secondary to a sellar tumor and according to the clinical presentation and the IRM, the histopahological examination of biopsies is mandatory to have a precise diagnosis. [less ▲]

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See detailPrise en charge du médulloblastome de l'enfant
Fransolet, Anne-Catherine; Born, Jacques Daniel; Misson, Jean-Paul ULiege et al

in Revue Médicale de Liège (2007), 62(4), 200-4

We present the experience of the Citadelle Hospital (Liege, B) in the diagnosis, treatment and follow-up of medulloblastoma in children. A retrospective study of 10 cases of medulloblastoma was performed ... [more ▼]

We present the experience of the Citadelle Hospital (Liege, B) in the diagnosis, treatment and follow-up of medulloblastoma in children. A retrospective study of 10 cases of medulloblastoma was performed. Five years after diagnosis, the event-free survival was 77%. [less ▲]

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See detailIdiopathic hypertrophic cranial pachymeningitis mimicking multiple meningiomas: case report and review of the literature.
Deprez, Manuel ULiege; Born, Jacques; Hauwaert, Cécile ULiege et al

in Acta Neuropathologica (1997), 94(4), 385-9

A case of idiopathic hypertrophic cranial pachymeningitis with an unusual and misleading manifestation is reported. Computed tomography scan, angiographic and magnetic resonance imaging findings were ... [more ▼]

A case of idiopathic hypertrophic cranial pachymeningitis with an unusual and misleading manifestation is reported. Computed tomography scan, angiographic and magnetic resonance imaging findings were suggestive of multiple meningeal neoplasms and a correct diagnosis was made only after meningeal biopsy. This 44-year-old patient had a previous history of an ill-defined systemic disorder associating episcleritis, erythroderma nodosa and multiple peripheral arthritis. We review previous reports of idiopathic cranial pachymeningitis with emphasis on radiological investigation techniques, histopathology and possible dysimmune mechanisms of pathogenesis. [less ▲]

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