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1.
Rev Neurol ; 24(127): 306-10, 1996 Mar.
Artículo en Español | MEDLINE | ID: mdl-8742397

RESUMEN

Hiccoughs (singultus) is a habitual physiological phenomenon, the persistence of which might indicate neurological and extraneurological multiple lesions. Its activation involves starting up numerous central and peripheral mechanisms which have yet to be clearly determined. Hiccoughs results from an intermittent myoclonus of the diaphragm, reflex in origin, with unknown authentic cause or physiological significance. It has been suggested that, more than just an abnormal reflex, it could be a type of myoclonus brought on by repeated activity of the 'solitary inspiratory nucleus', by releasing control of the inhibiting-activating upper nervous system activity. We present the case of a patient with uncontrollable hiccoughs lasting over six years as a result of paramedial bilateral thalamic ischaemia (rostral occlusion syndrome of the basilar artery type 1) of cardioembolic origin (auricular fibrillation) secondary to hyperthyroidism.


Asunto(s)
Arteriopatías Oclusivas/complicaciones , Arteriopatías Oclusivas/fisiopatología , Arteria Basilar/fisiopatología , Hipo/etiología , Administración Oral , Anticoagulantes/administración & dosificación , Anticoagulantes/uso terapéutico , Arteriopatías Oclusivas/diagnóstico , Hipo/tratamiento farmacológico , Humanos , Hipertiroidismo/complicaciones , Hipertiroidismo/diagnóstico , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad
2.
Rev Neurol ; 23(119): 145-7, 1995.
Artículo en Español | MEDLINE | ID: mdl-8548611

RESUMEN

Hepatolenticular degeneration, also known as Wilson's disease (WD), is an infrequent hereditary disorder which is transmitted in recessive autosomic fashion: its genetic defect is to be found in the long branch of chromosome 13 (13q14.3) and allows disorder to take place which has not been sufficiently clarified, in the bilious excretion of the copper (Cu) which is deposited in an anomalous manner on a level with different organic tissues, giving rise to characteristic clinical manifestations which are, basically, of a neurological, hepatic, psychiatric and ocular nature. We present the case of a young patient whose case began, four years ago, with depressive-type manifestations, with diagnosis only being made now. Our opinion on the early detection of asymptomatic patients is commented on, along with that concerning the effectiveness and safety of therapeutic alternatives to D-penicilamine.


Asunto(s)
Corteza Cerebral/fisiopatología , Degeneración Hepatolenticular/tratamiento farmacológico , Degeneración Hepatolenticular/fisiopatología , Trientina/uso terapéutico , Adulto , Ventrículos Cerebrales/anomalías , Cromosomas Humanos Par 13 , Cobre/sangre , Femenino , Degeneración Hepatolenticular/diagnóstico , Humanos , Imagen por Resonancia Magnética , Tomografía Computarizada por Rayos X , Trientina/administración & dosificación
3.
Neurologia ; 9(4): 133-40, 1994 Apr.
Artículo en Español | MEDLINE | ID: mdl-8018343

RESUMEN

Occlusion of the top of the basilar artery causes infarctions in supra- and infra-tentorial regions (thalamus, occipito-temporal lobes, rostral trunk and cerebellum) with characteristic clinical and radiological manifestations. We studied 17 patients with this syndrome whose clinical data and neurological images led us to classify them into four groups: type I (2 patients, 12%), showing mainly alterations in consciousness and ocular motricity, and bilateral thalamic infarction; type II (6 patients, 35%), with campimetric manifestations and uni- or bilateral ischemia of the occipito-temporal lobes; type III (5 patients, 29%), with associated corticospinal deficits and lacunar images in the rostral brainstem; and type IV (4 patients, 24%) with symptoms of and neuro-images revealing lesions in the cerebellum. The proposed classification is an attempt to facilitate diagnosis by neuro-imaging and to group patients according to prognosis.


Asunto(s)
Arteria Basilar/fisiopatología , Encefalopatías/fisiopatología , Anciano , Encéfalo/diagnóstico por imagen , Encéfalo/fisiopatología , Encefalopatías/complicaciones , Encefalopatías/diagnóstico , Isquemia Encefálica/etiología , Isquemia Encefálica/fisiopatología , Femenino , Lateralidad Funcional , Hemianopsia/etiología , Hemianopsia/fisiopatología , Hemiplejía/etiología , Hemiplejía/fisiopatología , Humanos , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Lóbulo Occipital/fisiopatología , Pronóstico , Trastornos Psicomotores/etiología , Trastornos Psicomotores/fisiopatología , Radiografía , Tálamo/fisiopatología
4.
Arch Neurobiol (Madr) ; 55(4): 188-92, 1992.
Artículo en Español | MEDLINE | ID: mdl-1417425

RESUMEN

Spontaneous intracerebellar haematomas are a relatively unusual cause of haemorrhagic stroke. The uncommon variety of vermian haematomas (5%) represents a serious diagnostic and treatment challenge and its outcome is generally poor, being the result of rapid elevation of intracranial pressure and brainstem compression. A rare case of spontaneous vermian haematoma with benign course without surgery is reported, including the results of neuroimaging tests.


Asunto(s)
Enfermedades Cerebelosas/complicaciones , Hemorragia Cerebral/complicaciones , Hematoma/terapia , Anciano , Anciano de 80 o más Años , Ataxia Cerebelosa/etiología , Enfermedades Cerebelosas/diagnóstico , Enfermedades Cerebelosas/patología , Hemorragia Cerebral/diagnóstico , Hemorragia Cerebral/patología , Diagnóstico Diferencial , Hematoma/complicaciones , Hematoma/diagnóstico , Hematoma/patología , Humanos , Imagen por Resonancia Magnética , Masculino , Vértigo/diagnóstico , Vértigo/etiología
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