RESUMEN
Although patients with isolated oral syndrome or facial sensory loss following stroke of thalamic ventroposteromedial (VPM) nucleus have been reported, there have been no reports of numbness in the tip of the tongue and lower lip. Furthermore, symptoms in the tip of the tongue caused by stroke are typically characterized as gustatory sensory disturbances. A 62-year-old hypertensive man experienced an acute onset of severe numbness in the left tip of the tongue and ipsilateral lower lip. Neurological examination revealed no other abnormalities except for the aforementioned numbness. Head computed tomography showed a small hematoma in the medial part of the right thalamus, most likely within the VPM nucleus. The somatosensory impulse of the tongue is conveyed via the lingual nerve, and it reaches the contralateral medial VPM proper via the trigeminal spinal nucleus. Therefore, thalamic stroke mainly involving the medial VPM proper has the potential to elicit numbness in the tip of the tongue. A major portion of the VPM nucleus is vascularized by the inferolateral arteries. The inferolateral arteries vary greatly in the number and position of the arteries and their tributaries, and small-vessel disease in this territory can present with diverse symptoms because of this complexity. These findings indicate that central neurological involvement should not be overlooked in the case of sensory disturbance restricted to the tip of the tongue and lip.
Asunto(s)
Hipoestesia/etiología , Hemorragias Intracraneales/complicaciones , Labio/inervación , Umbral Sensorial , Enfermedades Talámicas/complicaciones , Lengua/inervación , Núcleos Talámicos Ventrales/fisiopatología , Humanos , Hipoestesia/diagnóstico , Hipoestesia/fisiopatología , Hemorragias Intracraneales/diagnóstico , Hemorragias Intracraneales/fisiopatología , Masculino , Persona de Mediana Edad , Enfermedades Talámicas/diagnóstico , Enfermedades Talámicas/fisiopatología , Tomografía Computarizada por Rayos X , Núcleos Talámicos Ventrales/diagnóstico por imagenRESUMEN
Here, we report brain abscess due to Fusobacterium necrophorum (F. necrophorum) in a 78-year-old healthy man. He developed convulsion and did not have any signs of meningitis. Although the brain magnetic resonance imaging findings of the left occipital lobe were typical of a brain abscess, his cerebrospinal fluid examination revealed only slight pleocytosis and mild increase in protein levels. Thus, it was difficult to rule out the possibility of metastatic brain tumor; the patient's condition was provisionally diagnosed as symptomatic epilepsy secondary to brain abscess. His convulsion disappeared soon after administration of antiepileptic, antibacterial, and steroid agents. A craniotomy was performed to evacuate the abscess, and F. necrophorum was identified by culturing the abscess contents. After the operation, he was treated with appropriate antibacterial agents, which resulted in resolution of the brain abscess. Although Fusobacterium species are gram-negative anaerobic bacilli commensal of the human oropharynx, we need to recognize that Fusobacterium species can be a primary pathogen causing brain abscesses and may leave residual neurological sequelae without early appropriate treatment.
Asunto(s)
Absceso Encefálico/complicaciones , Absceso Encefálico/microbiología , Infecciones por Fusobacterium/complicaciones , Infecciones por Fusobacterium/microbiología , Fusobacterium necrophorum , Convulsiones/etiología , Anciano , Ampicilina/administración & dosificación , Antibacterianos/administración & dosificación , Absceso Encefálico/diagnóstico , Absceso Encefálico/tratamiento farmacológico , Infecciones por Fusobacterium/diagnóstico , Infecciones por Fusobacterium/tratamiento farmacológico , Fusobacterium necrophorum/aislamiento & purificación , Humanos , Masculino , Meningitis Bacterianas , Sulbactam/administración & dosificación , Terapéutica , Tomografía Computarizada por Rayos XAsunto(s)
Encéfalo/metabolismo , Encéfalo/patología , Proteínas de Unión al ADN/metabolismo , Neuronas/patología , Ataxias Espinocerebelosas , Proteínas Adaptadoras Transductoras de Señales/metabolismo , Salud de la Familia , Femenino , Humanos , Cuerpos de Inclusión/metabolismo , Cuerpos de Inclusión/patología , Masculino , Persona de Mediana Edad , Péptidos/metabolismo , Proteína Sequestosoma-1 , Ataxias Espinocerebelosas/genética , Ataxias Espinocerebelosas/metabolismo , Ataxias Espinocerebelosas/patologíaRESUMEN
BACKGROUND: Multiple system atrophy (MSA) has been considered a sporadic disease, without patterns of inheritance. OBJECTIVE: To describe the clinical features of 4 multiplex families with MSA, including clinical genetic aspects. DESIGN: Clinical and genetic study. SETTING: Four departments of neurology in Japan. Patients Eight patients in 4 families with parkinsonism, cerebellar ataxia, and autonomic failure with age at onset ranging from 58 to 72 years. Two siblings in each family were affected with these conditions. MAIN OUTCOME MEASURES: Clinical evaluation was performed according to criteria by Gilman et al. Trinucleotide repeat expansion in the responsible genes for the spinocerebellar ataxia (SCA) series and for dentatorubral-pallidoluysian atrophy (DRPLA) was evaluated by polymerase chain reaction. Direct sequence analysis of coding regions in the alpha-synuclein gene was performed. RESULTS: Consanguineous marriage was observed in 1 of 4 families. Among 8 patients, 1 had definite MSA, 5 had probable MSA, and 2 had possible MSA. The most frequent phenotype was MSA with predominant parkinsonism, observed in 5 patients. Six patients showed pontine atrophy with cross sign or slitlike signal change at the posterolateral putaminal margin or both on brain magnetic resonance imaging. Possibilities of hereditary ataxias, including SCA1 (ataxin 1, ATXN1), SCA2 (ATXN2), Machado-Joseph disease/SCA3 (ATXN1), SCA6 (ATXN1), SCA7 (ATXN7), SCA12 (protein phosphatase 2, regulatory subunit B, beta isoform; PP2R2B), SCA17 (TATA box binding protein, TBP) and DRPLA (atrophin 1; ATN1), were excluded, and no mutations in the alpha-synuclein gene were found. CONCLUSIONS: Findings in these multiplex families suggest the presence of familial MSA with autosomal recessive inheritance and a genetic predisposition to MSA. Molecular genetic approaches focusing on familial MSA are expected to provide clues to the pathogenesis of MSA.
Asunto(s)
Atrofia de Múltiples Sistemas/genética , Atrofia de Múltiples Sistemas/patología , Anciano , Encéfalo/patología , Consanguinidad , Salud de la Familia , Femenino , Predisposición Genética a la Enfermedad , Humanos , Japón , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Linaje , Análisis de Secuencia de ADN , Expansión de Repetición de Trinucleótido , alfa-Sinucleína/genéticaRESUMEN
Polyglutamine diseases are hereditary neurodegenerative disorders that are caused by the expansion of a CAG repeat in the causative genes. They comprise at least nine disorders, including DRPLA, HD, and Machado-Joseph disease. Initially, the discovery of neuronal intranuclear inclusions (NIIs) in human brains and in a murine model of HD provided a plausible hypothesis that the expression of expanded polyglutamine stretches leads to NII formation, resulting in neuronal cell death in selective brain regions characteristic to each disease. Recent studies, however, suggest that nuclear dysfunction, especially transcriptional abnormalities caused by the diffuse intranuclear accumulation of mutant proteins, plays a pivotal role in the development and progression of clinical symptoms. Polyglutamine diseases have a similarity with neuronal storage disease, and this pathological process might become a target for the establishment of an effective therapy for these diseases.
Asunto(s)
Encéfalo/patología , Trastornos Heredodegenerativos del Sistema Nervioso/patología , Cuerpos de Inclusión Intranucleares/metabolismo , Epilepsias Mioclónicas Progresivas/patología , Péptidos/metabolismo , Animales , Encéfalo/metabolismo , Muerte Celular/fisiología , Modelos Animales de Enfermedad , Trastornos Heredodegenerativos del Sistema Nervioso/metabolismo , Humanos , Ratones , Ratones Transgénicos , Epilepsias Mioclónicas Progresivas/metabolismo , Degeneración Nerviosa/metabolismo , Degeneración Nerviosa/patología , Neuronas/metabolismo , Neuronas/patología , Expansión de Repetición de TrinucleótidoRESUMEN
Periaxin (PRX) plays an important role in the myelination of the peripheral nerve and consequently in the pathogenesis of Charcot-Marie-Tooth disease (CMT). To date, nine nonsense or frameshift PRX mutations have been reported in eight families with CMT. The patients with PRX mutations appeared to show characteristic clinical features with early onset but slow or no progression, a common result of mutations that lead to missing a C-terminal acidic domain. Here, we report a Japanese CMT patient with these characteristic clinical features, who was a compound heterozygote for PRX R1070X and L132FsX153 mutations. We previously reported that three Japanese isolated families also had the homozygous R1070X mutation. To examine the potential founder effect of the R1070X mutation in the Japanese population, we performed haplotype analysis and found that each R1070X allele lay on a different haplotype background in these four families. Therefore, the high frequency of the R1070X mutation among the Japanese population is not likely the consequence of a founder effect, but probably a result of a mutation hot spot.
Asunto(s)
Enfermedad de Charcot-Marie-Tooth/genética , Proteínas de la Membrana/genética , Mutación , Adulto , Edad de Inicio , Alelos , Axones/ultraestructura , Cromatografía Líquida de Alta Presión , ADN/sangre , ADN/genética , Femenino , Marcadores Genéticos , Haplotipos , Heterocigoto , Homocigoto , Humanos , Japón , Masculino , Proteínas de la Membrana/análisis , Repeticiones de Microsatélite , Madres , Fibras Nerviosas Mielínicas/ultraestructura , Ácidos Nucleicos Heterodúplex , Linaje , Análisis de Secuencia de ADNRESUMEN
We report a 51-year-old man genetically diagnosed as Charcot-Marie-Tooth disease type 4F. The patient was the first child of healthy, consanguineous parents. He had two sisters and one of them showed similar but milder symptoms. He had gait disturbance since childhood. Then he noticed muscle weakness of his hands at the age of early forties, and more difficulties in gait at the age of late forties. On examination at age 51, he showed absence of all deep tendon reflexes, weakness of the hand and distal leg muscles, pes cavus and decreased sensitivity to touch and vibration in the lower extremities. Electrophysiological studies of the median nerve showed delayed motor nerve conduction velocity and undetectable sensory nerve action potentials. The histology of his sural nerve revealed moderate loss of large myelinated fibers and the diameters of residual fibers shifted to small shown as size-frequency histogram. Many fibers are thinly myelinated and some of the Schwann cells looked as wrapping around the myelinate fibers with their processes. On gene analyses, we identified an Arg 1070 Stop homozygous mutation in the Periaxin, known to be a causative gene for CMT type 4F. Based on these observations, we emphasized that broad genetic analyses are necessary for diagnosis of CMT disease, including so far unidentified mutations among the Japanese populations.
Asunto(s)
Enfermedad de Charcot-Marie-Tooth/genética , Proteínas de la Membrana/genética , Mutación , Enfermedad de Charcot-Marie-Tooth/diagnóstico , Consanguinidad , Genes Recesivos , Humanos , Masculino , Persona de Mediana Edad , LinajeRESUMEN
Intracranial lipomas are believed to be congenital malformations rather than true neoplasms, resulting from the abnormal differentiation of the meninx primitiva, the undifferentiated mesenchyme. We report here the surgical pathological features of a lipoma that was located on the cerebral surface of an abnormally formed fissure, and the underlying cortex of the middle temporal gyrus of a 20-year-old woman. The mass was composed of typical adipose tissue in which a large number of blood vessels were present. Thick connective tissue associated with the arachnoid membrane covered the cortical surface. The cortex exhibited a polymicrogyric configuration in which the cortical ribbon was abnormally undulated and excessively folded. Reelin-immunolabeled Cajal-Retzius-cell-like cells were observed frequently in the fused molecular layer. The cortical lamination underlying the molecular layer was poorly defined. Along the border between the connective tissue and cortical surface, there was a narrow zone in which the mesenchymal and neuronal tissues were intermingled, and where immunohistochemical and ultrastructural investigations disclosed disruption of the basal lamina, prominent astrocytosis, and abundant axonal and synaptic profiles. These findings suggest that focal disturbances in cerebral cortical development occur in association with the development of lipomas.
Asunto(s)
Neoplasias Encefálicas/patología , Lipoma/patología , Lóbulo Temporal/patología , Adulto , Neoplasias Encefálicas/metabolismo , Neoplasias Encefálicas/cirugía , Calbindina 2 , Moléculas de Adhesión Celular Neuronal/metabolismo , Proteínas de la Matriz Extracelular/metabolismo , Femenino , Proteína Ácida Fibrilar de la Glía/metabolismo , Humanos , Inmunohistoquímica/métodos , Antígeno Ki-67/metabolismo , Laminina/metabolismo , Lipoma/metabolismo , Lipoma/cirugía , Imagen por Resonancia Cinemagnética/métodos , Microscopía Electrónica de Transmisión/métodos , Proteínas del Tejido Nervioso/metabolismo , Proteínas de Neurofilamentos/metabolismo , Parvalbúminas/metabolismo , Proteína Reelina , Proteína G de Unión al Calcio S100/metabolismo , Serina Endopeptidasas/metabolismo , Coloración y Etiquetado/métodos , Sinaptofisina/metabolismo , Lóbulo Temporal/metabolismo , Lóbulo Temporal/cirugía , Lóbulo Temporal/ultraestructuraRESUMEN
Periaxin (PRX) plays a significant role in the myelination of the peripheral nerve. To date, seven non-sense or frameshift PRX mutations have been reported in six pedigrees with Dejerine-Sottas neuropathy or severe Charcot-Marie-Tooth neuropathy (CMT). We detected a PRX mutation in three patients in the screening of 66 Japanese demyelinating CMT patients who were negative for the gene mutation causing dominant or X-linked demyelinating CMT. Three unrelated patients were homozygous for a novel R1070X mutation and presented early-onset but slowly progressive distal motor and sensory neuropathies. Mutations lacking the carboxyl-terminal acidic domain may show loss-of-function effects and cause severe demyelinating CMT.
Asunto(s)
Enfermedad de Charcot-Marie-Tooth/genética , Proteínas de la Membrana/genética , Mutación , Adulto , Edad de Inicio , Preescolar , Cromatografía Líquida de Alta Presión , Cromosomas Humanos X , Codón sin Sentido , Análisis Mutacional de ADN , Progresión de la Enfermedad , Femenino , Mutación del Sistema de Lectura , Genes Dominantes , Ligamiento Genético , Homocigoto , Humanos , Japón , Masculino , Persona de Mediana Edad , Estructura Terciaria de Proteína , Factores de TiempoRESUMEN
We report a homozygous case of spinocerebellar ataxia type 17 with 48 glutamines. The age of the patient at disease onset was not lower than those of heterozygotes with the same CAG-repeat sizes, but the clinical manifestations were rapidly progressive dementia and chorea. Neuronal loss was relatively restricted and most prominent in the Purkinje cell layer and striatum; however, intranuclear neuronal polyglutamine accumulation was widespread, with a high frequency in the cerebral cortex and striatum.