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4.
Radiologia ; 49(5): 351-4, 2007.
Artigo em Espanhol | MEDLINE | ID: mdl-17910874

RESUMO

We report the case of a patient that presented with an intense headache caused by a subarachnoid hemorrhage. Magnetic resonance angiography demonstrated the existence of an aneurysm of the left posterior communicating artery, as well as of a persistent primitive trigeminal artery.


Assuntos
Aneurisma Intracraniano/diagnóstico , Imageamento por Ressonância Magnética , Feminino , Humanos , Aneurisma Intracraniano/complicações , Pessoa de Meia-Idade , Hemorragia Subaracnóidea/etiologia
5.
Radiología (Madr., Ed. impr.) ; 49(5): 351-354, sept. 2007. ilus
Artigo em Es | IBECS | ID: ibc-69703

RESUMO

Exponemos el caso de una paciente que presentó cefalea intensa debida a una hemorragia subaracnoidea. La angiorresonancia magnética puso de manifiesto la existencia de un aneurisma de la arteria comunicanteposterior izquierda, así como de una arteria trigeminal primitiva persistente


We report the case of a patient that presented with an intense headache caused by a subarachnoid hemorrhage. Magnetic resonance angiography demonstrated the existence of an aneurysm of the left posteriorcommunicating artery, as well as of a persistent primitive trigeminal artery


Assuntos
Humanos , Feminino , Pessoa de Meia-Idade , Aneurisma Intracraniano/diagnóstico , Imageamento por Ressonância Magnética , Hemorragia Subaracnóidea/etiologia , Aneurisma Intracraniano/complicações
8.
Radiologia ; 48(5): 313-5, 2006.
Artigo em Espanhol | MEDLINE | ID: mdl-17168242

RESUMO

The giant diverticulum of the colon is a rare entity first diagnosed by Bouvin and Bonte in 1946. Few cases have been reported in the literature. It is normally located in the antimesenteric border of the sigmoid colon. In most cases it is considered to be an uncommon complication of a common disease: colonic diverticulosis. We present a case of giant diverticulum of the sigma diagnosed in an 80-year-old man and we describe the plain-film and CT findings.


Assuntos
Diverticulose Cólica/diagnóstico , Idoso de 80 Anos ou mais , Humanos , Masculino
9.
Radiología (Madr., Ed. impr.) ; 48(5): 313-315, sept. 2006. ilus
Artigo em Es | IBECS | ID: ibc-049416

RESUMO

El divertículo gigante de colon es una rara entidad diagnosticada por primera vez por Bouvin y Bonte en 1946. Desde entonces pocos casos han sido descritos en la literatura. Se localiza habitualmente en el borde antimesentérico del sigma. La mayoría se considera una complicación infrecuente de una enfermedad común, la diverticulosis colónica. Presentamos un caso de divertículo gigante de sigma diagnosticado en un varón de 80 años y describimos los hallazgos en la radiología simple y tomografía computarizada


The giant diverticulum of the colon is a rare entity first diagnosed by Bouvin and Bonte in 1946. Few cases have been reported in the literature. It is normally located in the antimesenteric border of the sigmoid colon. In most cases it is considered to be an uncommon complication of a common disease: colonic diverticulosis. We present a case of giant diverticulum of the sigma diagnosed in an 80-year-old man and we describe the plain-film and CT findings


Assuntos
Masculino , Idoso , Humanos , Divertículo do Colo/diagnóstico , Tomografia Computadorizada por Raios X/métodos , Colo Sigmoide/patologia , Diverticulose Cólica/complicações
13.
Rev Neurol ; 41(2): 86-90, 2005.
Artigo em Espanhol | MEDLINE | ID: mdl-16028186

RESUMO

INTRODUCTION: Cortical development disorders constitute a group of entities resulting from an interruption in the development of the central nervous system. Most of them derive from the stoppage of migration, but proliferation and organisation can also be affected. Heterotopia is the most frequent of all migration disorders. CASE REPORTS: We describe three cases of familial periependymal heterotopia consisting in three sisters who, after having seizures in infancy, were submitted to a magnetic resonance (MR) scan that revealed isointense nodules in the cortical grey matter in all the MR sequences. They were diagnosed as having periependymal heterotopia. The existence of a history of early onset seizures in the family of the mother supported the diagnosis of familial heterotopia. CONCLUSIONS: Heterotopia is the most frequently occurring anomaly affecting cortical development and, of these, the periependymal form is the most common. Periependymal heterotopia may be determined by sex-linked inheritance (X chromosome). It is considered to be one of the most common congenital disorders in familial and early onset epilepsy. MR is the preferred diagnostic technique, since its high resolution allows it to identify and characterise heterotopias.


Assuntos
Encefalopatias/complicações , Encéfalo/anormalidades , Coristoma/complicações , Epêndima/patologia , Epilepsia/etiologia , Agenesia do Corpo Caloso , Animais , Encéfalo/patologia , Encéfalo/fisiopatologia , Encefalopatias/congênito , Encefalopatias/patologia , Criança , Coristoma/congênito , Coristoma/patologia , Cromossomos Humanos X/genética , Proteínas Contráteis/genética , Epilepsia/patologia , Epilepsia/fisiopatologia , Feminino , Filaminas , Humanos , Lactente , Imageamento por Ressonância Magnética , Proteínas dos Microfilamentos/genética , Ratos , Tomografia Computadorizada por Raios X
14.
Rev. neurol. (Ed. impr.) ; 41(2): 86-90, 16 jul., 2005. ilus
Artigo em Es | IBECS | ID: ibc-039117

RESUMO

Introducción. Los trastornos del desarrollo corticalconstituyen un grupo de entidades que son consecuencia de la interrupcióndel desarrollo del sistema nervioso central. La mayoríaderiva de la detención de la migración, pero también pueden verseafectadas la proliferación y la organización. Dentro de los trastornosde la migración, la heterotopía es el más frecuente. Casos clínicos.Presentamos tres casos de heterotopía periependimaria familiar,tres hermanas a las que, tras sufrir una crisis en la infancia, seles realizó sendas resonancias magnéticas (RM), por las que seapreciaron nódulos isointensos a la sustancia gris cortical en todaslas secuencias de RM, y se les diagnosticó heterotopía periependimaria.La existencia de antecedentes en la familia materna de crisisde inicio precoz apoya el diagnóstico de heterotopía familiar.Conclusión. La heterotopía es la anomalía del desarrollo corticalmás frecuente y, dentro de ella, lo es la forma periependimaria. Laheterotopía periependimaria puede venir determinada por unaherencia ligada al sexo (cromosoma X). Se considera uno de lostrastornos congénitos más comunes en la epilepsia familiar y decomienzo precoz. La RM es la técnica diagnóstica que se elige, porsu gran resolución, ya que es capaz de identificar y caracterizar lasheterotopías


Introduction. Cortical development disorders constitute a group of entities resulting from an interruption in thedevelopment of the central nervous system. Most of them derive from the stoppage of migration, but proliferation andorganisation can also be affected. Heterotopia is the most frequent of all migration disorders. Case reports. We describe threecases of familial periependymal heterotopia consisting in three sisters who, after having seizures in infancy, were submitted toa magnetic resonance (MR) scan that revealed isotense nodules in the cortical grey matter in all the MR sequences. They werediagnosed as having periependymal heterotopia. The existence of a history of early onset seizures in the family of the mothersupported the diagnosis of familial heterotopia. Conclusions. Heterotopia is the most frequently occurring anomaly affectingcortical development and, of these, the periependymal form is the most common. Periependymal heterotopia may be determinedby sex-linked inheritance (X chromosome). It is considered to be one of the most common congenital disorders in familial andearly onset epilepsy. MR is the preferred diagnostic technique, since its high resolution allows it to identify and characteriseheterotopias


Assuntos
Feminino , Criança , Humanos , Epilepsia/complicações , Epilepsia/genética , Córtex Cerebral/anormalidades , Córtex Cerebral/patologia , Telencéfalo/anormalidades , Telencéfalo/patologia , Prognóstico , Imageamento por Ressonância Magnética
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