Assuntos
Dracunculoidea/isolamento & purificação , Elasmobrânquios , Doenças dos Peixes/patologia , Meningite/veterinária , Infecções por Spirurida/veterinária , Animais , Feminino , Doenças dos Peixes/diagnóstico , Doenças dos Peixes/parasitologia , Meningite/diagnóstico , Meningite/parasitologia , Meningite/patologia , São Cristóvão e Névis , Infecções por Spirurida/diagnóstico , Infecções por Spirurida/parasitologia , Infecções por Spirurida/patologiaRESUMO
Cryptococcosis by Cryptococcus gattii occurs mainly in immunocompetent hosts, however, during the last decades, a growing number of cases in immunocompromised individuals have been noticed around the world. This report presents epidemiological, clinical and outcome aspects of patients with cryptococcosis caused by this species from a non-endemic area in Brazil. Of 278 Cryptococcus spp. clinical isolates recovered during the same period, 267 (96%) were molecularly identified as Cryptococcus neoformans VNI genotype and 11 (4%) as C. gattii VGII genotype by URA-5 RFLP. Of the 11 C. gattii patients, eight were male, mean age of 47.5 years. Of these, four were HIV-infected, one was kidney transplanted, one presented low CD4+ T cells values of unknown cause, another presented chronic liver disease meanwhile the remaining four were apparently immunocompetent. Disseminated disease and cryptococcal meningitis were present in four patients each. Most patients received amphotericin B plus fluconazole. Seven out of the 11 patients cured and four died before or during the therapy. The increased number of individuals with cryptococcosis by this species during the last decades needs to be carefully evaluated specially those who are HIV-infected. Nevertheless, Cryptococcus species differentiation is currently relevant in order to better know their relation with geographical, clinical host preference and outcome particularities.
Assuntos
Criptococose/epidemiologia , Criptococose/patologia , Cryptococcus gattii/isolamento & purificação , Adulto , Idoso , Anfotericina B/administração & dosagem , Antifúngicos/administração & dosagem , Brasil/epidemiologia , Criptococose/tratamento farmacológico , Criptococose/microbiologia , Cryptococcus gattii/classificação , Cryptococcus gattii/genética , DNA Fúngico/genética , Feminino , Fluconazol/administração & dosagem , Genótipo , Humanos , Infecções Fúngicas Invasivas/tratamento farmacológico , Infecções Fúngicas Invasivas/epidemiologia , Infecções Fúngicas Invasivas/microbiologia , Infecções Fúngicas Invasivas/patologia , Masculino , Meningite/tratamento farmacológico , Meningite/epidemiologia , Meningite/microbiologia , Meningite/patologia , Pessoa de Meia-Idade , Polimorfismo de Fragmento de Restrição , Estudos Retrospectivos , Análise de Sobrevida , Resultado do Tratamento , Adulto JovemRESUMO
OBJECTIVE: To describe clinical cases with neurological manifestations associated with Borrelia burgdorferi infection in a large cohort of children and adults from Mexico. MATERIAL AND METHODS: Patients with neurological manifestation (cranial neuritis, radiculoneuritis, meningitis and encephalomyelitis) were recruited in one pediatric and two general hospitals, during January 2006-December 2015. Blood and cerebrospinal fluid (CSF) samples were drawn from each patient at inclusion. IgM and IgG antibodies against B. burgdorferi were detected using a commercial ELISA test, and confirmed by Western-Blot test (WB) using three different antigens from Borrelia burgdorferi complex. Following CDC criteria were considered true cases with both positive tests. RESULTS: Of 606 patients recruited, 403 (66.5%) were adults and 203 (33.4%) children, 50.5% were male. B. burgdorferi infection was diagnosed in 168 patients (27.7%), 97 adults, mean age 42 ± 14.7 years and 71 children, mean age 9.6 ± 5 years; early disseminated disease occurred in 130 cases (77.4 %) and chronic stage in 38 (22.6 %). A previous tick bite was reported by 21% cases, and 5% recalled an erythema migrans lesion. Polyradiculoneuropathy and encephalomyelitis were the most common manifestations, whereas 14.8% presented an initial Guillain-Barré Syndrome. B. burgdorferi sensu stricto was identified in 142 (84%) cases, B. garinii in 14 (8%), B. afzelii in three, and nine cases presented coinfection with two species. CONCLUSION: Lyme neuroborreliosis is a frequent condition in patients with neurological diseases in Mexico.
Assuntos
Borrelia burgdorferi/isolamento & purificação , Encefalomielite/patologia , Neuroborreliose de Lyme/epidemiologia , Neuroborreliose de Lyme/patologia , Meningite/patologia , Neurite (Inflamação)/patologia , Radiculopatia/patologia , Adolescente , Adulto , Western Blotting , Criança , Pré-Escolar , Encefalomielite/microbiologia , Ensaio de Imunoadsorção Enzimática , Feminino , Humanos , Neuroborreliose de Lyme/microbiologia , Masculino , Meningite/microbiologia , México/epidemiologia , Pessoa de Meia-Idade , Neurite (Inflamação)/microbiologia , Radiculopatia/microbiologia , Picadas de Carrapatos/microbiologia , Adulto JovemRESUMO
A 43-year-old male with a history of eosinophilic angiocentric fibrosis presented with headache and double vision since 48 h. Idiopathic hypertrophic pachymeningitis was diagnosed based on nuclear magnetic resonance and comprehensive systemic study findings. Eosinophilic angiocentric fibrosis and idiopathic hypertrophic pachymeningitis have been associated with IgG4-related diseases, but this was the first case in which they coexisted in the same patient. After steroid treatment failure, rituximab was used with excellent results.
Assuntos
Eosinófilos/patologia , Meningite/diagnóstico , Adulto , Biópsia , Fibrose , Humanos , Hipertrofia/complicações , Hipertrofia/diagnóstico , Hipertrofia/patologia , Imageamento por Ressonância Magnética , Masculino , Meningite/complicações , Meningite/patologiaRESUMO
ABSTRACT A 43-year-old male with a history of eosinophilic angiocentric fibrosis presented with headache and double vision since 48 h. Idiopathic hypertrophic pachymeningitis was diagnosed based on nuclear magnetic resonance and comprehensive systemic study findings. Eosinophilic angiocentric fibrosis and idiopathic hypertrophic pachymeningitis have been associated with IgG4-related diseases, but this was the first case in which they coexisted in the same patient. After steroid treatment failure, rituximab was used with excellent results.
RESUMO Um homem de 43 anos, com história de fibrose angiocêntrica eosinofílica, apresentou cefaléia e visão dupla com 48 horas. A paquimeningite hipertrófica idiopática foi diagnosticada com base na ressonância magnética nuclear e em achados sistêmicos abrangentes no estudo. A fibrose angiocêntrica eosinofílica e a paquimeningite hipertrófica idiopática foram associadas a doenças relacionadas à IgG4, mas este foi o primeiro caso em que elas coexistiram no mesmo paciente. Após a falha do tratamento com esteroides, o rituximabe foi usado com excelentes resultados.
Assuntos
Humanos , Masculino , Adulto , Eosinófilos/patologia , Meningite/diagnóstico , Biópsia , Fibrose , Imageamento por Ressonância Magnética , Hipertrofia/complicações , Hipertrofia/diagnóstico , Hipertrofia/patologia , Meningite/complicações , Meningite/patologiaRESUMO
INTRODUÇÃO: Em 2010, a vacina conjugada 10-valente (PCV10) foi incorporada ao programa nacional de imunizações (PNI) brasileiro. Este imunobiológico confere imunização contra os dez principais tipos capsulares de Streptococcus pneumoniae, patógeno responsável por diversas manifestações clínicas e com elevada contribuição nas taxas de incidência e mortalidade por meningite, que é a condição clínica mais grave. OBJETIVO: O presente estudo teve como objetivo avaliar o impacto da PCV10 na epidemiologia da meningite pneumocócica na região metropolitana de Salvador (RMS) Bahia, comparando o período anterior (2008-2010) e posterior (2011-2013) a sua utilização, bem como realizar uma caracterização molecular minuciosa a partir de uma série histórica (1996-2012) entre os isolados resistentes a enicilina (PNSSP com CIM≥ 0,125 μg/mL) e para os sorotipos não-vacinais (2008-2012). MATERIAL E MÉTODOS: Foram incluídos todos casos de meningite pneumocócica confirmados laboratorialmente no período entre 1996 a 2013. Taxas de incidência para a Salvador e RMS foram calculadas com base nos dados populacionais do IBGE/2010. A determinação do tipo capsular foi realizada através da técnica de Multiplex-PCR e/ou reação de Quellung. A sensibilidade a nove antimicrobianos foi testada através das técnicas disco-difusão,microdiluição e E-test. Para caracterizar o perfil molecular foram aplicadas as técnicas de genotipagem de PFGE e MLST. RESULTADOS: Um total de 939 casos de meningite pneumocócica foram identificados no período de 1996-2013, sendo que 70 casos ocorrem entre 2011 a 2013 (período pós-vacinal). A incidência de meningite pneumocócica em todas as faixas etárias na RMS reduziu de 0,70 casos/100.000 habitantes para 0,59 casos/100.000 habitantes considerando o período de três anos antes e após a vacinação com PCV10 [p<0,05; RR IC 95%: 1,46 (1,03-2,05)]. Esta redução foi significativa na faixa etária de 0-2 anos e nos casos por sorotipos relacionados à PCV10. Não houve aumento significativo de casos por sorotipos não vacinais nesta casuística,apesar do surgimento de casos por sorotipos não-vacinais não detectados anteriormente na série histórica de MP (10F, 21, 22F, 15A e 24F). Os isolados resistentes à penicilina analisados na série histórica se restringiram a 13 sorotipos, entre os quais: 14 (45,1 %; 78/173), 23F (19,1%; 33/173), 6B (14,4 %; 25/173), 19F (9,2 %; 16/173) e 19A (5,2 %; 9/173). 94% dos casos nãosusceptíveis à penicilina (PNSSP) foram de sorotipos vacinais. Os grupos clonais caracterizados pelo PFGE/MLST predominantes ao longo dos anos foram representados pelo sorotipo 14, denominado grupo A/ST 66 [35,3 %(61/173)] e grupo GK/ST 156 [4.6 % (8/173)], este último associado com níveis elevados de resistência a penicilina e ceftriaxona. Não foram detectados grupos clonais emergentes associados a tipos capsulares não-vacinais.CONCLUSÕES: Estes achados sugerem que a introdução da PCV10 modificou a epidemiologia da meningite pneumocócica na população estudada.
INTRODUCTION: In 2010, the 10-valent pneumococcal conjugate vaccine (PCV10) was introduced into the Brazilian national immunization program (NIP). This immunobiological provides immunization against the main ten capsular types of Streptococcus pneumoniae, the pathogen responsible for different clinical manifestations and high contribution in the incidence and mortality from meningitis, which is the most severe clinical condition. OBJECTIVE: This study aimed to evaluate the impact of PCV10 in the epidemiology of pneumococcal meningitis in the metropolitan area of Salvador (RMS) Bahia, comparing the previous (2008-2010) and after (2011-2013) periods its use, as well as conduct a thorough molecular characterization from a historical series (1996-2012) among isolates resistant to penicillin (PNSSP with CIM≥ 0.125 g / ml) and nonvaccine serotypes (2008-2012). MATERIAL AND METHODS: We included all cases of pneumococcal meningitis laboratory confirmed for the period 1996 to 2013. Incidence rates for Salvador and RMS were calculated based on population data from IBGE/2010. The capsular type determination was performed by multiplex PCR and/or Quellung reaction. Isolates Nine antibiotics were tested by disk-diffusion test, broth micro-dilution and E-test. To characterize the molecular profiling techniques were applied genotyping PFGE and MLST...
Assuntos
Meningite/complicações , Meningite/diagnóstico , Meningite/imunologia , Meningite/mortalidade , Meningite/patologia , Meningite/prevenção & controle , Meningite/virologia , Streptococcus pneumoniae , Streptococcus pneumoniae/imunologia , Streptococcus pneumoniae/químicaRESUMO
Eosinophilic meningitis caused by Angiostrongylus cantonensis is an endemic and emerging disease that affects adults and children in Jamaica. Most cases resolve without sequelae, but young children are at high risk of neurological damage and death. Treatment with corticosteroids and albendazole is considered safe for adults and children, but protocols for its use in children have not been established. A 19-month-old infant with permanent neurological sequlae caused by Angiostrongylus cantonensis meningitis is reported, and five other Jamaican cases are summarized. A review of the literature of children with permanent neurological sequlae and death is presented. Children <5 years (especially <2) were at increased risk of incomplete recovery and death if they presented with bulbar signs, flaccid paresis and coma. None of the severe or fatal cases received early intervention with anthelminthics, and disease progression was not altered with corticosteroids. In view of the pathophysiology, necropsy reports and animal studies, it seems that the early use of larvicidals may change the course of severe presentations.
Assuntos
Angiostrongylus cantonensis/isolamento & purificação , Eosinofilia/diagnóstico , Eosinofilia/patologia , Meningite/diagnóstico , Meningite/patologia , Infecções por Strongylida/diagnóstico , Infecções por Strongylida/patologia , Corticosteroides/uso terapêutico , Fatores Etários , Animais , Anti-Helmínticos/uso terapêutico , Anti-Inflamatórios/uso terapêutico , Doenças Endêmicas , Eosinofilia/epidemiologia , Eosinofilia/parasitologia , Feminino , Humanos , Lactente , Jamaica/epidemiologia , Meningite/epidemiologia , Meningite/parasitologia , Infecções por Strongylida/epidemiologia , Infecções por Strongylida/parasitologia , Análise de SobrevidaAssuntos
Humanos , Masculino , Feminino , Cuidados Críticos , Meningite/diagnóstico , Meningite/etiologia , Meningite/patologia , Meningite/reabilitação , MeningiteRESUMO
OBJECTIVES: To report a case of multifocal fibrosclerosis with a nine-year follow up, and to discuss this disease's radiological appearance and management. The disease is a rare systemic disorder of unknown cause characterised by fibrous proliferation involving multiple anatomical sites. CASE REPORT: A 50-year-old woman presented with histological findings characterised by similar inflammatory processes involving the meninges, pituitary gland, peritoneum, retroperitoneum and orbits, prompting a search for a common pathophysiology. A diagnosis of multifocal fibrosclerosis was postulated. Symptom improvement was noted after treatment with prednisone and azathioprine. CONCLUSION: This is the first documented case of involvement of the cochleovestibular nerve in a patient with multifocal fibrosclerosis. The rare association between fibrotic diseases and masses showing various clinical patterns should be kept in mind by otolaryngologists, and imaging performed to investigate for multifocal fibrosclerosis. However, diagnosis can only be confirmed with tissue biopsy and histopathological examination.
Assuntos
Meningite/patologia , Fibrose Retroperitoneal/congênito , Transtornos de Sensação/complicações , Doenças do Nervo Vestibulococlear/patologia , Azatioprina/uso terapêutico , Biópsia , Diagnóstico Diferencial , Progressão da Doença , Feminino , Glucocorticoides/uso terapêutico , Humanos , Imunossupressores/uso terapêutico , Imageamento por Ressonância Magnética , Meningite/complicações , Meningite/diagnóstico , Pessoa de Meia-Idade , Doenças Orbitárias/complicações , Doenças Orbitárias/diagnóstico por imagem , Doenças Orbitárias/patologia , Prednisona/uso terapêutico , Radiografia , Recidiva , Fibrose Retroperitoneal/complicações , Fibrose Retroperitoneal/diagnóstico , Fibrose Retroperitoneal/patologia , Fibrose Retroperitoneal/terapia , Convulsões/complicações , Transtornos de Sensação/patologia , Sinusite/complicações , Doenças do Nervo Vestibulococlear/complicaçõesRESUMO
Neonatal meningitis is an illness characterized by inflammation of the meninges and occurring within the birth and the first 28 days of life. Invasive infection by Streptococcus pneumoniae, meningitis and sepsis, in neonate is associated with prolonged rupture of membranes; maternal colonization/illness, prematurity, high mortality and 50% of cases have some form of disability. For this purpose, we measured brain levels of TNF-α, IL-1ß, IL-6, IL-10, CINC-1, oxidative damage, enzymatic defense activity and the blood-brain barrier (BBB) integrity in neonatal Wistar rats submitted to pneumococcal meningitis. The cytokines increased prior to the BBB breakdown and this breakdown occurred in the hippocampus at 18 h and in the cortex at 12h after pneumococcal meningitis induction. The time-dependent association between the complex interactions among cytokines, chemokine may be responsible for the BBB breakdown and neonatal pneumococcal severity.
Assuntos
Barreira Hematoencefálica/fisiopatologia , Regulação da Expressão Gênica/fisiologia , Mediadores da Inflamação/metabolismo , Meningite , Infecções Pneumocócicas/complicações , Animais , Animais Recém-Nascidos , Córtex Cerebral/metabolismo , Córtex Cerebral/microbiologia , Córtex Cerebral/patologia , Modelos Animais de Doenças , Hipocampo/metabolismo , Hipocampo/microbiologia , Hipocampo/patologia , Meningite/etiologia , Meningite/metabolismo , Meningite/patologia , Ratos , Fatores de TempoRESUMO
Neisseria meningitidis es agente causal de meningitis y meningococcemia. Se realizó la presente investigación a fin de analizar fenotípicamente las cepas invasivas de N. meningitidis aisladas en Cumaná, estado Sucre. Se incluyó el total de cepas identificadas como N. meningitidis en el laboratorio de bacteriología del Hospital Universitario Antonio Patricio de Alcalá, durante los años 2009-2010; provenientes de muestras de líquido cefalorraquídeo (LCR) y sangre (hemocultivos). A cada aislamiento se le determinó la susceptibilidad antimicrobiana y el serogrupo respectivo. Durante el período en estudio se analizaron 10 cepas, de las cuales 5 provenían de LCR. El ensayo de susceptibilidad antimicrobiana reveló que las cepas presentaban sensibilidad a penicilina, cefotaxima, meropenem, rifampicina, ciprofloxacina y cloranfenicol siendo sólo resistentes al trimetoprim/ sulfametoxazol. El serogrupo más frecuente fue el B (8 cepas), aislándose un caso de serogrupo Y. Respecto al grupo etario de los pacientes, de las 10 cepas, 8 provenían de pacientes pediátricos. Este es el primer estudio con cepas de N. meningitidis aisladas en Cumaná, por lo que se hace imprescindible el análisis permanente de las cepas aisladas en la zona, con fines de monitoreo, principalmente, de la susceptibilidad antimicrobiana y los serogrupos circulantes.
Neisseria meningitidis is the causal agent for meningitis and meningococcemia. This research was performed to phenotypically analyze invasive strains of N. meningitidis isolated in Cumana, State of Sucre. The study included all strains identified as N. meningitidis isolated in the bacteriology laboratory at the University Hospital Antonio Patricio de Alcalá, during the years 2009-2010, coming from cerebrospinal fluid (CSF) samples and blood cultures. For each isolate, the antimicrobial susceptibility and respective serogroup were determined. During the period of study, 10 strains were analyzed, of which 5 came from CSF. The antimicrobial susceptibility test revealed that the strains showed sensitivity to penicillin, cefotaxime, meropenem, rifampicin, ciprofloxacin and chloramphenicol; they were resistant only to trimethoprim/ sulfamethoxazole. Serogroup B was the most frequent (8 strains); one case of serogroup Y was isolated. Regarding the patients ages, of the 10 strains, 8 were found in pediatric patients. This is the first study about strains of N. meningitidis isolated in Cumaná, so it is essential that permanent research regarding the strains isolated in the area is carried out for monitoring purposes, mainly in terms of antimicrobial susceptibility and the circulating serogroups.
Assuntos
Anti-Infecciosos , Meningite/patologia , Neisseria meningitidis Sorogrupo B/isolamento & purificação , Neisseria meningitidis Sorogrupo Y/isolamento & purificaçãoRESUMO
BACKGROUND: Management of communicating hydrocephalus associated with infectious meningitis and arachnoiditis of the basal cisterns can be challenging if no microorganism or pathological diagnosis is established. The purpose of our series is to elucidate the efficacy of endoscopic basal cistern exploration, biopsy, and endoscopic third ventriculostomy (ETV) in patients with basal cistern meningitis and hydrocephalus. METHODS: Between 2005 and 2010, all patients who underwent transventricular endoscopic exploration biopsy and biopsy of the basal cisterns were analyzed and prospectively followed up. Particular attention was given to neuroendoscopic findings, sensitivity of biopsy, and the role of ETV. RESULTS: Twenty-four patients, ranging in age from 2 to 63 years, underwent transventricular endoscopic biopsy and exploration of the basal cisterns. All patients had negative cerebrospinal fluid analysis obtained by lumbar puncture. Successful ETV, exploration, dissection, and biopsy of the basal cisterns were performed successfully in all patients with a flexible neuroendoscope. Neuroendoscopic findings included: unusually thick Liliequist membrane, moderate to severe adhesive arachnoiditis, inflammatory and cotton-like exudates, granulations, and narrow subarachnoid space. Definitive histopathological diagnosis from the basal cisterns specimen was obtained in 79% of patients. There were no complications related to the procedure. At 15 months of follow-up, 70% of the patients with hydrocephalus did not require a ventriculoperitoneal shunt. CONCLUSIONS: Endoscopic transventricular basal cisterns exploration is feasible with a flexible neuroendoscope. It is a viable alternative in the management of patients with basal cistern meningitis and arachnoiditis without histopathological diagnosis. It yields to an accurate diagnosis in 79% of the patients. ETV is a good alternative in the management of intracisternal extraventricular obstructive hydrocephalus.
Assuntos
Ventrículos Cerebrais/cirurgia , Hidrocefalia/patologia , Hidrocefalia/cirurgia , Meningite/patologia , Meningite/cirurgia , Neuroendoscopia/métodos , Adolescente , Adulto , Idoso , Anestesia Geral , Aracnoide-Máter/patologia , Aracnoidite/cirurgia , Biópsia , Córtex Cerebral/patologia , Córtex Cerebral/cirurgia , Líquido Cefalorraquidiano/química , Líquido Cefalorraquidiano/citologia , Criança , Pré-Escolar , Estudos de Coortes , Dura-Máter/patologia , Feminino , Seguimentos , Humanos , Imageamento por Ressonância Magnética , Masculino , Meningite/complicações , Transtornos Mentais/etiologia , Transtornos Mentais/psicologia , Pessoa de Meia-Idade , Tomografia Computadorizada por Raios X , Resultado do TratamentoRESUMO
La paquimeningitis hipertrófica idiopática crónica y la estenosis traqueal subglótica idiopática son raras condiciones de origen desconocido. En ambas existen un proceso inflamatorio fibrótico que afecta respectivamente, la duramadre y la traquea. La paquimeningitis hipertrófica idiopática crónica en forma típica, causa parálisis progresiva de nervios craneales, cefaleas, hipertensión intracraneal o disfunción cerebelosa. En la estenosis traqueal subglótica idiopática, usualmente limitada a la región subglótica y los dos primeros anillos traqueales, los sintomas son variables incluyendo disnea progresiva, sibilancias y estribor notables sobre el cuello. La paquimeningitis hipertrófica idiopática crónica ocurre en pacientes de todas las edades y el examen de elección para detectarla es la resonancia magnética cerebral, en tanto que la estenosis traqueal subglótica idiopática suele afectar mujeres jóvenes o maduras y es mejor evidenciada mediante tomografía computarizada. El diagnóstico es uno de exclusión. Deben descartarse enfermedades infecciosas como tuberculosis y lúes, y otras como sarcoidosis, carcinomatosis meníngea o vasculitis. Suelen responder inicialmente a los corticosteroides pero puede haber recurrencia al suspenderlos. La evolución a largo plazo es incierta. Este trabajo informa acerca de una paciente en quien ambas condiciones se dieron cita, discutiéndose sus manifestaciones clínicas, radiológicas y patológicas. Aunque considerada esencial para el diagnóstico, en nuestro caso no se realizó una biopsia meníngea. Planteamos la posibilidad de una asociación entre ambas condiciones, por su inicio simultáneo con recaídas, por su condición de inflamación crónica y recurrente y su respuesta a los corticosteroides.
Chronic idiopathic hypertrophic paquimeningitis and chronic subglottic tracheal stenosis are rare conditions of unknown origin. In both there is a fibrotic inflammatory process affecting, respectively the dura mater and the trachea. The chronic idiopathic hypertrophic paquimeningitis in its typical presentation causes progressive paralysis of cranial nerves, headaches, intracranial hypertensión or cerebellar dysfunction. In the chronic subglottic tracheal stenosis, usually limited to the subglottic region and the two first traqueal rings, its symptoms are variable including progressive shortness of breath, wheezing and stridor notable on the neck. The chronic idiopathic hypertrophic paquimeningitis occurs in patients of all ages and the test of choice for diagnosis it is the brain magnetic resonance image, while the chronic subglottic tracheal stenosis usually affect young or mature women and is best evidenced by computerizide tomography scan. The diagnósis is one of exclusion. Infectious diseases such as tuberculosis and lues, and others as sarcoidosis, meningeal carcinomatosis or vasculitides should be discarded. Often initially respond to corticosteroids but may have recurrences when stopped. The evolution in the long term is uncertain. This paper reports on a patient with both conditions, discussing their clinical, radiological and pathological manifestation. Although considered essential for the diagnosis, in our case was not performed a meningeal biopsy. We postulate the possibility of association between these two conditions, based in their simultaneous onset, the occurence of relapses in both diseases, its condition of recurrent and chronic inflammation, and its response to corticosteroids.
Assuntos
Humanos , Feminino , Adulto , Asma/diagnóstico , Diplopia/etiologia , Dor Ocular/diagnóstico , Dura-Máter/lesões , Estenose Traqueal/patologia , Inflamação/etiologia , Meningite/patologia , Acuidade Visual/fisiologia , Dispneia/etiologia , Espectroscopia de Ressonância Magnética/métodos , OftalmologiaRESUMO
Neonatal group B streptococcus meningitis causes neurologic morbidity and mortality. Cerebrovascular involvement is a common, poorly studied, and potentially modifiable pathologic process. We hypothesized that imaging patterns of focal brain infarction are recognizable in neonatal group B streptococcal meningitis. A consecutive case series included term neonates with the following: (1) bacterial meningitis, (2) acute group B streptococcal infection (positive cerebrospinal fluid/blood culture), (3) brain magnetic resonance imaging within 14 days, and (4) acute intraparenchymal focal infarctions (restricted diffusion). Lesions within known arterial territories were classified as arterial ischemic stroke. Clinical presentations, investigations, and neurologic outcomes were recorded. Eight newborns (50% female) with focal infarction were identified. Five presented early (<1 week), and all manifested clinical shock and elevated acute-phase reactants. Less than 50% had prenatal group B streptococcal screening, while 2 of 3 screened were negative. Two distinct patterns of focal infarction were identified: (1) deep perforator arterial stroke to basal ganglia, thalamus, and periventricular white matter (7/8, 88%), and (2) superficial injury with patchy, focal infarctions of the cortical surface (6/8, 75%). Outcomes (mean 23.8 months) were poor, with severe disability or death in 6/8 (75%). Recognizable stroke patterns contribute to severe neurologic outcomes and represent a potentially modifiable pathophysiologic process in neonatal group B streptococcal meningitis.
Assuntos
Proteínas de Bactérias/líquido cefalorraquidiano , Meningite/complicações , Infecções Estreptocócicas/complicações , Acidente Vascular Cerebral/etiologia , Feminino , Humanos , Recém-Nascido , Imageamento por Ressonância Magnética/métodos , Masculino , Meningite/patologia , Estudos Retrospectivos , Infecções Estreptocócicas/líquido cefalorraquidiano , Acidente Vascular Cerebral/classificação , Acidente Vascular Cerebral/patologiaRESUMO
Los Virus Herpes Simple son responsables de una variedad de infecciones a nivel de mucosas bucal y genital, son neurotrópicos, capaces de alojarse en células nerviosas y permanecer latentes con subsecuentes reactivaciones, en algunos casos pueden provocar meningitis y encefalitis. tienen una morbilidad significativa y una mortalidad elevada. El presente estudio tiene como objetivo determinar la incidencia de VHS en la etiología de los síndromes agudos del SNC mediante la detección en suero y LCR de anticuerpos específicos. Se estudiaron 93 muestras pareadas de pacientes con afecciones neurológicas que mostraron resultados negativos en el estudio bacteriológico de LCR y cuya relación Alb-LCR/Alb-suero fue <0,0075. Los anticuerpos fueron detectados por el método de inmunoensayo enzimático Elisa: Enzygnost® anti virus VHS/IgM-IgG (Behring, 1994), donde 1,2% (1/93) de las muestras de suero resultaron positivas para IgM; 89,24% (83/93)de los sueros resultaron positivos para IgG; y 27,39% (20/93) de las muestras de LCR presentaron anti-IgG positivo. La presencia de IgG en LCR sugiere la producción intratecal de estos anticuerpos en el SNC, lo que muestra una participación importante de este agente viral en las infecciones y enfermedades asociadas al SNC
Herpes simplex viruses are agents responsible for a variety of infections on buccal and genital mucosa; they are neurotropic, capable of lodging in the nerve cells and remaining latent with subsequent reactivations; in some cases, they can provoke meningitis and encephalitis; and they have a significant morbidity and are associated with a high mortality. The present project aims to determine HSVs effect on the etiology of acute central nervous system (CNS) syndromes using the detection of specific antibodies in serum and cerebrospinal fluid. The 93 paired samples from patients with neurological affectations studied demonstrated negative results in the LCR bacteriological study and their Alb-LCR/Alb-serum relation was < 0.0075. Antibodies were detected by the enzymatic immunoassay ELISA method, where 1.2% (1/93) of the serum samples turned out positive for IgM; 89.24% (83/93) of the serum samples resulted positive for IgG; and 27.39% (20/93) of LCR samples were positive for anti-IgG. IgG presence in LCR suggested the intrathecal production of these antibodies inside the CNS, which demonstrates a significant participation by this viral agent in infections and diseases associated with the CNS
Assuntos
Humanos , Anticorpos/uso terapêutico , Encefalite por Herpes Simples/patologia , Herpes Simples/virologia , Líquido Cefalorraquidiano/fisiologia , Meningite/patologia , Meningite/virologia , Sistema Nervoso Central/patologia , Sistema Nervoso Central/virologia , Soro/virologia , Ensaio de Imunoadsorção Enzimática/métodosRESUMO
INTRODUCTION: Hypertrophic pachymeningitis is a clinical condition that is caused by a diffuse or localised thickening of the dura mater. It predominantly affects males and manifests as chronic headache, with or without association to neurological manifestations, such as paralysis of the cranial nerves, cerebellar ataxia and neuro-ophthalmic complications. CASE REPORT: A 61-year-old male, with no relevant past history, who, one month before admission, had begun to suffer from right frontotemporal headache that irradiated to the ipsilateral orbital region and was more pronounced at night. A week later he was affected by a decrease in visual acuity in the right eye and two weeks later he noted the presence of right palpebral ptosis, while the headaches increased. The examination showed: right palpebral ptosis with global ophthalmoparesis with predominance of adduction and abduction, and diminished photomotor reflex in the right eye. The visual acuity of the right eye was reduced and the palpebral fissure was 0 in the right eye. The fundus oculi was normal. Infectious and non-infectious causations of meningitis were precluded. Magnetic resonance imaging revealed a diffuse thickening of the supratentorial and infratentorial meninges, as well as diffuse uptake of the paramagnetic substance; thickening of the mucus in both paranasal maxillary sinuses was also observed. A meningeal biopsy study confirmed the existence of hypertrophic pachymeningitis. Treatment was established with prednisone and the clinical symptoms improved. CONCLUSIONS: Idiopathic hypertrophic pachymeningitis is an underdiagnosed condition that must be taken into consideration in cases of patients with a history of subacute or chronic meningitis in which infectious and non-infectious causations have been precluded, and high-dose steroid treatment must be established.
Assuntos
Meningite/diagnóstico , Meningite/patologia , Blefaroptose/etiologia , Seio Cavernoso/patologia , Cefaleia/etiologia , Humanos , Masculino , Seio Maxilar/patologia , Meninges/patologia , Meningite/complicações , Pessoa de Meia-Idade , Oftalmoplegia/etiologiaRESUMO
El objetivo del trabajo es cuantificar la magnitud de casos de meningitis sin diagnóstico etiológico especificado. Identificar la prevalencia de los agentes causantes en los diferentes grupos etáreos y según sexo. Señalar las características clínicas de los casos observados y vacunas recibidas. Conocer la relación entre meningitis y patologías asociadas.
Assuntos
Humanos , Adolescente , Recém-Nascido , Lactente , Pré-Escolar , Criança , Distribuição de Qui-Quadrado , Infecções Meningocócicas/etiologia , Infecções Pneumocócicas/etiologia , Meningite/diagnóstico , Meningite/etiologia , Meningite/patologia , Vacinas Bacterianas/administração & dosagemRESUMO
Las vacunas conjugadas contra Haemophilus influenzae tipo b (Hib) son la herramienta más importante para prevenir la mayoría de las enfermedades invasoras producidas por dicho patógeno, pero debido a su costo, aún no se han introducido mundialmente de manera masiva. En el presente estudio se determinó la relación costo-efectividad de una vacuna contra Hib para prevenir la neumonía y la meningitis bacterianas en niños menores de 2 años en Colombia.
Assuntos
Humanos , Haemophilus influenzae tipo b , Vacinas Anti-Haemophilus , Meningite por Haemophilus , Meningite/patologiaRESUMO
A 7-year-old, otherwise healthy Peruvian boy presented with a 3-month history of an indurated centrofacial plaque. Histologic examination revealed a granuloma containing free-living amebae tentatively identified as Balamuthia mandrillaris. The patient failed to respond to tentative treatment. He was admitted to the intensive care unit 7 months later with neurologic manifestations of granulomatous amebic encephalitis, which proved fatal. The difficulty in diagnosing this rare presentation of cutaneous amebiasis, the challenge of treating the condition, and the morbidity and high mortality associated with cerebral involvement are discussed.