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No disponible
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Humanos , Masculino , Adulto , Imageamento por Ressonância Magnética , Síndrome de Cimitarra/diagnósticoRESUMO
No disponible
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Masculino , Pessoa de Meia-Idade , Humanos , Córtex Cerebral/fisiopatologia , Epilepsias Parciais/fisiopatologia , Coristoma/diagnóstico , Espectroscopia de Ressonância MagnéticaRESUMO
No disponible
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Feminino , Adulto , Humanos , Apendicite , Apendicite , Doenças Peritoneais , Doenças Peritoneais , Doenças do Colo , Omento , Anormalidade Torcional , Tomografia Computadorizada por Raios XRESUMO
INTRODUCTION: Brucellosis is a form of anthropozoonosis that is found the world over. It has a particularly high incidence rate in Spain, above all in rural areas such as Extremadura, Castile and Leon, Castile-La Mancha and Aragon, largely due to the consumption of non-pasteurised milk and cheese. Neurobrucellosis can be defined as a set of either early or late neurological complications caused by Brucella. It is difficult to determine its frequency, although it oscillates between 2-18% of all cases of brucellosis. CASE REPORTS: We report the cases of four patients diagnosed as having neurobrucellosis. The different presenting clinical symptoms, the complementary explorations, treatment and duration are all described. CONCLUSIONS: The clinical features of neurobrucellosis vary greatly and, in general, tend to be chronic. Many of the laboratory procedures usually employed in the diagnosis of brucellosis frequently give negative results. For these reasons, and because it is a disease that is both treatable and curable, the degree of suspicion must be high, especially in endemic areas, so that an early diagnosis can be made to allow suitable treatment to be established.
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Brucelose , Adolescente , Adulto , Idoso , Animais , Antibacterianos/uso terapêutico , Brucella , Brucelose/diagnóstico , Brucelose/tratamento farmacológico , Brucelose/fisiopatologia , Bovinos , Diagnóstico Diferencial , Feminino , Humanos , Masculino , Pessoa de Meia-IdadeAssuntos
Veia Axilar , Veia Subclávia , Trombose Venosa/diagnóstico por imagem , Adulto , Humanos , Masculino , Síndrome , UltrassonografiaRESUMO
No disponible
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Masculino , Adulto , Humanos , Veia Axilar , Veia Subclávia , Trombose Venosa , SíndromeRESUMO
INTRODUCTION: Idiopathic hypertrophic cranial pachymeningitis (IHCP) is a rare and little known form of chronic inflammation of the dura mater, the pathogenesis of which remains unclear. CASE REPORT: We report the case of a 77-year-old male who was admitted to hospital after suffering a stroke; following the findings in the MR imaging, the patient was diagnosed as having IHCP. Treatment with corticoids led to an improvement in the patient's condition both clinically and radiologically. CONCLUSIONS: IHCP produces a non-nodular diffuse dural thickening that is hypointense with respect to the brain parenchyma in all the MRI sequences with intravenous contrast enhancement.
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Meningite , Trombose Venosa/complicações , Idoso , Humanos , Imunossupressores/uso terapêutico , Imageamento por Ressonância Magnética , Masculino , Meningite/diagnóstico , Meningite/tratamento farmacológico , Meningite/etiologia , Meningite/patologia , Trombose Venosa/patologiaRESUMO
INTRODUCTION: Listeria monocytogenes is a gram-positive bacillus which causes sporadic infections in immunocompromised humans, with a special propensity for the central nervous system, in the form of acute, subacute or chronic meningitis, rhombencephalitis or abscesses in the brain or spinal cord. The final diagnosis is established by germ culture in blood or in cerebrospinal fluid (CSF). Preferred treatment is ampicillin in association with aminoglycosides. CASE REPORT: We report the case of a 70-year-old male patient with a history of arterial hypertension and chronic lymphatic leukaemia with no specific treatment, who suffered meningoencephalitis and brain abscesses caused by L. monocytogenes. Symptoms were a 48-hour history of headache and a febrile condition. The CSF showed lymphocytic pleocytosis with hypoglycorrhachia. Magnetic resonance scans of the brain revealed areas of cerebritis and multiple brain abscesses in the right frontal lobe. Specific treatment was established with ampicillin for 13 weeks, associated with gentamicin and vancomycin during the first few weeks, until x-rays showed the lesions to be resolved. CONCLUSIONS: L. monocytogenes infections must be investigated in all patients with cellular immunosuppression who present febrile symptoms. The central nervous system may be the only area of the body infected. Moreover, this site will need studying in patients who present neurological focus data or an alteration in the state of consciousness and bacteraemia due to L. monocytogenes. Establishing suitable treatment as early as possible can improve the prognosis.
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Abscesso Encefálico , Listeria monocytogenes , Listeriose/diagnóstico , Listeriose/patologia , Idoso , Antibacterianos/uso terapêutico , Abscesso Encefálico/diagnóstico , Abscesso Encefálico/microbiologia , Abscesso Encefálico/patologia , Humanos , Listeriose/tratamento farmacológico , Imageamento por Ressonância Magnética , MasculinoAssuntos
Morte Súbita , Síncope , Criança , Humanos , Síndrome do QT Longo/complicações , Masculino , Síncope/etiologiaRESUMO
No disponible
