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hallucinations/главоболие
Линкът е запазен в клипборда
Страница 1 от 285 резултата
Olfactory hallucinations in primary headache disorders: case series and literature review.
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BACKGROUND
Olfactory hallucinations (phantosmias) have rarely been reported in migraine patients. Unlike visual, sensory, language, brainstem, and motor symptoms, they are not recognized as a form of aura by the International Classification of Headache Disorders.
METHODS
We examined the clinical
Olfactory hallucination in childhood primary headaches: case series.
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BACKGROUND
Although olfactory hallucination (OH) has been reported in patients with primary headaches, olfactory aura has not been recognised by the International Classification of Headache Disorders (ICHD-2). In this study, we examined the frequency and characteristics of OH among children and
Hearing voices: does it give your patient a headache? A case of auditory hallucinations as acoustic aura in migraine.
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OBJECTIVE
Auditory hallucinations are generally considered to be a psychotic symptom. However, they do occur without other psychotic symptoms in a substantive number of cases in the general population and can cause a lot of individual distress because of the supposed association with schizophrenia.
Elementary visual hallucinations, blindness, and headache in idiopathic occipital epilepsy: differentiation from migraine.
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This is a qualitative and chronological analysis of ictal and postictal symptoms, frequency of seizures, family history, response to treatment, and prognosis in nine patients with idiopathic occipital epilepsy and visual seizures. Ictal elementary visual hallucinations are stereotyped for each
Auditory hallucinations associated with headaches following traumatic brain injury.
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A 60-year-old woman with headache, confusion, and hallucinations.
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A 46-year-old woman with a history of personality change, headache, and olfactory hallucination.
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Olfactory hallucinations in primary headache disorders: case series and literature review. A comment.
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Zolpidem, vascular headache, and hallucinations in an adolescent.
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[A case of occipital epilepsy with anti-GluRepsilon2 antibody in cerebrospinal fluid, presenting as repeated visual disturbance and headache].
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A 78-year-old man was admitted to our hospital with repeated attacks of headache and visual hallucinations, which had begun 10 days before. He also displayed left hemispatial neglect and left homonymous hemianopsia during attacks. Brain magnetic resonance imaging (MRI) showed an abnormal
[Multiple cerebral cavernous haemangiomas in a woman with visual hallucinations].
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Cerebral vascular malformations is a common condition though it remains clinically silent in the vast majority of patients. Symptoms comprise seizures, headaches, focal neurological deficits and unconsciousness due to major cerebral haemor-rhage. A 31-year-old woman was referred for assessment of
[Non-convulsive status with hemianopsia and ictal headaches: an uncommon manifestation of parieto-occipital epilepsy].
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BACKGROUND
Parieto-occipital epilepsy is uncommon disease that usually occurs with positive symptoms such as illusions, visual hallucinations. The pericital headache, with or without migraine-type characteristics, is common symptoms (amaurosis, hemianopsia) are rare.
METHODS
A 21 year-old woman with
Visual hallucinations in a case of reversible hypertension-induced brain oedema.
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Visual hallucinations are commonly associated with seizures, drug effects, psychiatric disorders, or visual loss as 'release' phenomena. We report the case of a previously healthy 65-year-old woman, who was admitted to hospital with intermittent headache episodes accompanied by complex visual
A Pounding Problem: A Case of Recurrent Headache Caused by Anti-NMDA Receptor Encephalitis
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Background: Anti-N-methyl-d-aspartate receptor (Anti-NMDAR) encephalitis is a serious autoimmune disease in which antibody production against the NMDA receptor results in profound neurotransmitter dysregulation. Patients may present with
Complex hallucinations and panic attacks in a 13-year-old with migraines: the alice in wonderland syndrome.
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This case report describes a 13-year-old girl whose family requested a referral from the pediatrician for Child and Adolescent Mental Health Services in order to understand her recent onset of bizarre behavior. On assessment, she was found to have episodes of complex audiovisual hallucinations and
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