dermoid cyst/seizures

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Heightened seizure susceptibility associated with brain dermoid cyst and the administration of human chorionic gonadotropin (hCG).

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It is known that the intramuscular injection of human chorionic gonadotropin (hCG) lowers the threshold for motor evoked responses (MEPs) in the first dorsal interosseous (FDI) muscle to transcranial magnetic stimulation (TMS) in humans. We describe the case of a patient with a clinically silent

Long-term Seizure Disorder Caused by a Dermoid Cyst with Catastrophic Developments.

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Glioblastoma multiforme (GBM) is a World Health Organization (WHO) grade IV primary malignant astrocytoma. Aneurysms are devastating intracranial neurovascular pathologies. Intracranial dermoid cysts are common, benign lesions which can be clinically silent or associated with seizure disorder. We

Febrile convulsions in an adult as presenting symptom of intracranial dermoid cyst: a case report.

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A 32-year-old man had generalized tonic-clonic epileptic seizures associated with episodes of recurrent high fever for 6 years. Repeated physical examinations including neurological status, EEG and nuclear brain scan were negative. Brain CT showed a non-homogeneous parasellar cyst of low density and

Ruptured central nervous system dermoid cyst of the suprasellar region manifesting as unusual epileptic seizure: a case report.

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Central nervous system dermoid cysts are very rare lesions derived from ectopic epithelial cells. They are slow-growing benign tumors, but may cause significant morbidity through compression of neurological and vascular vascular structures and, rarely, rupture into the subarachnoid space. We present

Ruptured intracranial dermoid cyst manifesting as new onset seizure: a case report.

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Intracranial dermoid cysts are rare tumors derived from ectopic epithelial cells. They are slow-growing benign entities, but can cause significant morbidity through compression of neurovascular structures and, rarely, rupture into the subarachnoid space. We present a rare case of a spontaneously

Ruptured frontal dermoid cyst: an unusual cause of seizure in a postpartum female.

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Rare cause of seizures: ruptured intracranial dermoid cyst.

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Phacomatosis pigmentokeratotica associated with a suprasellar dermoid cyst and leg hypertrophy.

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Phacomatosis pigmentokeratotica (PP) is a mosaic disorder that represents a distinct epidermal naevus syndrome. Its defining features are an epidermal naevus that is usually of the sebaceous type and a speckled lentiginous naevus arranged in a chequerboard pattern. In addition, there are

Nasal dermoid cyst with intracranial extension in a cat.

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An 11-month-old female neutered Ragdoll cat was presented for focal seizures, aggression and altered behaviour. A diagnosis of a nasal dermoid cyst with intracranial extension was made following MRI, cytology and histopathology. The cyst was surgically excised with a resolution of

Ruptured Intracranial Dermoid: Is Surgery Indispensible: 11-Year Follow-Up of a Rare Entity.

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BACKGROUND Dermoid cysts are rare intracranial lesions that can occasionally rupture into intraventricular and subarachnoid spaces and can present with a myriad of symptoms. The surgical intervention in such cases is demanding, because the disseminated contents are spread widely in intraventricular

'Teeth in the brain' - a case of giant intracranial mature cystic teratoma.

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The authors describe a case of a giant intracranial mature cystic teratoma in a 16-year-old girl presenting acutely with a severe headache, vomiting and a complex generalised seizure with a background history of intermittent headaches for 3 years. CT and MRI brain demonstrated a ruptured large

Nasofrontal dermoid sinus cyst: report of two cases.

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OBJECTIVE Nasofrontal dermoid sinus cysts are rare. The embryological origin, presentation, treatment, and genetic associations of two cases of these cysts are discussed. Emphasis is placed on physical findings and the importance of addressing both the intracranial and extracranial

Brainstem dermoid cyst rupture with hydrocephalus in a child.

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Intracranial dermoid cysts are ectodermal lesions of embryological origin. They are of slow progression and symptoms associated with unruptured cysts are most commonly due to mass effect. However, a potential rupture in the ventricular system is rare and can cause meningitis, seizures and

Dermoid sinus and cyst of the lip.

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Midline dermoid cysts, although rare, typically present as nasal or glabellar masses with potential sinus tract extension to the skin or to the central nervous system. Craniofacial dermoid cysts present in varied ways, including asymptomatic puncti, infection, or seizure secondary to intracranial

[Ruptured dermoid cyst]

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We report the case of a 28-year-old male admitted to the emergency department for generalized seizure. A brain computed tomography (CT) revealed a ruptured dermoid cyst of the supra-tentorial stage (multiple drop-shaped fat structures were found in the subarachnoid space, basal cisterns and in

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