encephalocele/crise epiléptica

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The varied semiology of seizures in the context of small anterior temporal encephaloceles.

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Small encephaloceles of the anterior temporal pole have been increasingly recognised as an underlying epileptogenic substrate in patients with medically refractory epilepsy. The current report aims to expand on the current knowledge by emphasising that seizure semiology in such patients can vary

Intractable complex partial seizures associated with occult temporal lobe encephalocele and meningoangiomatosis: a case report.

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Occult congenital temporal lobe encephalocele has rarely been reported in association with medically intractable complex partial seizures. The four previously reported cases were unsuspected preoperatively. We present the case of an 18-year-old woman with intractable complex partial seizures since

Temporal Lobe Encephaloceles: A Potentially Curable Cause of Seizures.

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OBJECTIVE Temporal lobe encephaloceles are characterized by protrusion of brain parenchyma through a structural defect in the floor of the middle fossa. They have been reported to cause cerebrospinal fluid (CSF) leaks, conductive hearing loss, meningitis, and seizures. The association between

A Case of Mesial Temporal Lobe Sclerosis Following Temporal Bone Encephalocele Repair for Medically Refractory Seizures.

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The aim of this report is to present a case of mesial temporal lobe sclerosis (MTS) causing medically refractory seizures, which was initially disguised as temporal lobe encephalocele secondary to prior otologic surgery. Temporal lobe encephaloceles are characterized by a defect within the middle

Cerebrospinal fluid rhinorrhea and seizure caused by temporo-sphenoidal encephalocele.

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This case report describes the symptoms and clinical course of a 35-year-old female patient who was diagnosed with a temporo-sphenoidal encephalocele. It is characterized by herniation of cerebral tissue of the temporal lobe through a defect of the skull base localized in the middle fossa. At the

Gyratory seizures as a presentation of temporal encephalocele.

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Gyratory seizures (GS) are rare and have been reported in focal (frontal and temporal) as well as generalized epilepsies. The exact neuroanatomical substrate of gyration during a seizure is not clearly understood, but is thought to be due to the involvement of the basal ganglia. The direction of

Basal transethmoidal encephalocele and malignant hypertension in a parturient with a seizure disorder. A case report.

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BACKGROUND Nasal encephaloceles are uncommon in North America and may be diagnosed only as incidental findings. The presence of an encephalocele and malignant hypertension in the parturient requires complex coordination of care. METHODS We present a case of severe chronic hypertension in a pregnant

Spontaneous motor cortex encephalocele presenting with simple partial seizures and progressive hemiparesis. Case report and review of the literature.

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Several cases of congenital or acquired temporal encephaloceles have been reported in the literature as the causative mechanism of simple and/or complex partial seizures. In this report the authors describe a rare case of spontaneous parietal encephalocele presenting with simple partial seizures and

Encephalocele-related seizures in adulthood: synergistic contributions of CT and MRI to the anatomic work-up.

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Frontal encephalocele in a middle-aged woman with first seizure: smells like a seizure to me.

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Temporal lobe encephaloceles: etiology of partial complex seizures?

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Aicardi syndrome associated with anterior cephalocele in a female infant.

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Aicardi syndrome is a triad of abnormalities that includes total or partial agenesis of the corpus callosum, chorioretinal lacunae, and infantile spasms. This syndrome was first described in 1965. A female infant with Aicardi syndrome associated with a nasoethmoidal cephalocele is described in this

[A case of transethmoidal meningocele showing increased activity of 99mTcHM-PAO at seizure attack].

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A case of transethmoidal meningocele presenting seizure attack is reported. A 59-year-old man was admitted to our hospital because of seizure attack. On admission, he was neurologically free without right olfactory dysfunction. T2-weighted image of MRI showed high intensity signal area in right

A systematic review of published evidence on expanded endoscopic endonasal skull base surgery and the risk of postoperative seizure.

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Although postoperative seizure is an acknowledged risk following transcranial surgery, the incidence of seizure after removal of intradural pathology via an expanded endoscopic endonasal approach is not well defined. The current study was performed to systematically review the risk of seizure in

Outlook for the child with a cephalocele.

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Specific information on the outcome for a child with a cephalocele can be difficult to find and interpret. To update outcome information for the child with a cephalocele, the investigators compared outcome of 34 infants from their institution with that of those in previously published series. For

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