Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
1.
Rev. bras. hematol. hemoter ; Rev. bras. hematol. hemoter;39(3): 202-209, July-Sept. 2017. tab, graf
Artigo em Inglês | LILACS | ID: biblio-898927

RESUMO

Abstract Background l-Asparaginase is essential in the treatment of childhood acute lymphoblastic leukemia. If immunoglobulin G anti-l-asparaginase antibodies develop, they can lead to faster plasma clearance and reduced efficiency as well as to hypersensitivity reactions, in which immunoglobulin E can also participate. This study investigated the presence of immunoglobulin G and immunoglobulin E anti-l-asparaginase antibodies and their clinical associations. Methods Under 16-year-old patients at diagnosis of B-cell acute lymphoblastic leukemia confirmed by flow cytometry and treated with a uniform l-asparaginase and chemotherapy protocol were studied. Immunoglobulin G anti-l-asparaginase antibodies were measured using an enzyme-linked immunosorbent assay. Intradermal and prick skin testing was performed to establish the presence of specific immunoglobulin E anti-l-asparaginase antibodies in vivo. Statistical analysis was used to investigate associations of these antibodies with relevant clinical events and outcomes. Results Fifty-one children were studied with 42 (82.35%) having anti-l-asparaginase antibodies. In this group immunoglobulin G antibodies alone were documented in 10 (23.8%) compared to immunoglobulin E alone in 18 (42.8%) patients. Immunoglobulin G together with immunoglobulin E were simultaneously present in 14 patients. Children who produced exclusively immunoglobulin G or no antibodies had a lower event-free survival (p-value = 0.024). Eighteen children (35.3%) relapsed with five of nine of this group who had negative skin tests suffering additional relapses (range: 2-4), compared to none of the nine children who relapsed who had positive skin tests (p-value < 0.001). Conclusion Children with acute lymphoblastic leukemia and isolated immunoglobulin G anti-l-asparaginase antibodies had a higher relapse rate, whereas no additional relapses developed in children with immunoglobulin E anti-l-asparaginase antibodies after the first relapse.


Assuntos
Asparaginase , Imunoglobulina E , Imunoglobulina G , Escherichia coli , Leucemia-Linfoma Linfoblástico de Células Precursoras , Anticorpos Neutralizantes , Hipersensibilidade
2.
Rev Bras Hematol Hemoter ; 39(3): 202-209, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28830598

RESUMO

BACKGROUND: l-Asparaginase is essential in the treatment of childhood acute lymphoblastic leukemia. If immunoglobulin G anti-l-asparaginase antibodies develop, they can lead to faster plasma clearance and reduced efficiency as well as to hypersensitivity reactions, in which immunoglobulin E can also participate. This study investigated the presence of immunoglobulin G and immunoglobulin E anti-l-asparaginase antibodies and their clinical associations. METHODS: Under 16-year-old patients at diagnosis of B-cell acute lymphoblastic leukemia confirmed by flow cytometry and treated with a uniform l-asparaginase and chemotherapy protocol were studied. Immunoglobulin G anti-l-asparaginase antibodies were measured using an enzyme-linked immunosorbent assay. Intradermal and prick skin testing was performed to establish the presence of specific immunoglobulin E anti-l-asparaginase antibodies in vivo. Statistical analysis was used to investigate associations of these antibodies with relevant clinical events and outcomes. RESULTS: Fifty-one children were studied with 42 (82.35%) having anti-l-asparaginase antibodies. In this group immunoglobulin G antibodies alone were documented in 10 (23.8%) compared to immunoglobulin E alone in 18 (42.8%) patients. Immunoglobulin G together with immunoglobulin E were simultaneously present in 14 patients. Children who produced exclusively immunoglobulin G or no antibodies had a lower event-free survival (p-value=0.024). Eighteen children (35.3%) relapsed with five of nine of this group who had negative skin tests suffering additional relapses (range: 2-4), compared to none of the nine children who relapsed who had positive skin tests (p-value<0.001). CONCLUSION: Children with acute lymphoblastic leukemia and isolated immunoglobulin G anti-l-asparaginase antibodies had a higher relapse rate, whereas no additional relapses developed in children with immunoglobulin E anti-l-asparaginase antibodies after the first relapse.

3.
PLoS One ; 11(12): e0168819, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-28030642

RESUMO

OBJECTIVE: The aim of this study was to evaluate whether the concentration of sCD40L, a product of platelet activation, correlates with the presence of Pseudomonas aeruginosa in the airway of patients with cystic fibrosis (CF) and to determine its possible clinical association. METHODS: Sixty patients with CF, ranging in age from 2 months to 36 years, were studied. The demographics, cystic fibrosis transmembrane conductance regulator (CFTR) genotype, spirometry measurements, radiographic and tomographic scans, platelet count in peripheral blood, sCD40L, IL-6, TNF-α and ICAM1 data were collected. Infection-colonization of the airway was evaluated using sputum and throat swab cultures; the levels of anti-Pseudomonas aeruginosa antibodies (Anti-PaAb) were evaluated. RESULTS: Patients with CF and chronic colonization had anti-PaAb values of 11.6 ± 2.1 ELISA units (EU) and sCD40L in plasma of 1530.9 ±1162.3 pg/mL; those with intermittent infection had 5.7 ± 2.7 EU and 2243.6 ± 1475.9 pg/mL; and those who were never infected had 3.46 ± 1.8 EU (p≤0.001) and 1008.1 ± 746.8 pg/mL (p≤0.01), respectively. The cutoff value of sCD40L of 1255 pg/mL was associated with an area under the ROC (receiver operating characteristic curve) of 0.84 (95% CI, 0.71 to 0.97), reflecting P. aeruginosa infection with a sensitivity of 73% and a specificity of 89%. Lung damage was determined using the Brasfield Score, the Bhalla Score, and spirometry (FVC%, FEV1%) and found to be significantly different among the groups (p≤0.001). CONCLUSION: Circulating sCD40L levels are increased in patients with cystic fibrosis and P. aeruginosa infection. Soluble CD40L appears to reflect infection and provides a tool for monitoring the evolution of lung deterioration.


Assuntos
Ligante de CD40/sangue , Ligante de CD40/química , Fibrose Cística/sangue , Fibrose Cística/microbiologia , Infecções por Pseudomonas/complicações , Pseudomonas aeruginosa/fisiologia , Adolescente , Criança , Pré-Escolar , Estudos de Coortes , Fibrose Cística/complicações , Feminino , Humanos , Lactente , Masculino , Curva ROC , Solubilidade , Adulto Jovem
4.
Dig Liver Dis ; 43(3): 204-8, 2011 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-20843755

RESUMO

BACKGROUND: Eosinophilic esophagitis (EoE) is not routinely considered in the differential diagnosis of refractory gastroesophageal reflux disease (GERD). AIMS: To prospectively evaluate the prevalence of EoE and describe the clinical features and predictors of EoE in patients with refractory symptoms of GERD. METHODS: Esophageal biopsies were obtained in patients with symptoms of GERD refractory to 8 weeks of conventional antisecretory therapy. Diagnosis of EoE was defined as at least 20 eosinophils × high power field and clinical unresponsiveness to proton pump inhibitors. Clinical and manometric features were compared. Independent risk factors predicting EoE were identified. RESULTS: Six out of 150 included patients (4%) met the diagnostic criteria for EoE. Patients with EoE were significantly younger, had significantly more dysphagia, atopy, ineffective esophageal peristalsis, esophageal rings and esophageal strictures than patients without EoE. Independent predictors of EoE were: age under 45 years (OR 4.8, 95% CI 2.4-8.6), dysphagia (OR 12.2, 95% CI 4.3-19.4), and atopy (OR 3.4, 95% CI 1.5-7.4). CONCLUSIONS: EoE is an uncommon condition (4%) in patients with refractory symptoms of GERD. Age under 45 years, atopy or dysphagia may warrant suspicion of EoE in this subset of patients.


Assuntos
Esofagite Eosinofílica/diagnóstico , Esofagite Eosinofílica/epidemiologia , Refluxo Gastroesofágico/complicações , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Biópsia , Diagnóstico Diferencial , Endoscopia do Sistema Digestório , Esofagite Eosinofílica/complicações , Esofagite Eosinofílica/patologia , Esôfago/patologia , Feminino , Refluxo Gastroesofágico/tratamento farmacológico , Humanos , Masculino , Manometria , Pessoa de Meia-Idade , Prevalência , Estudos Prospectivos , Fatores de Risco , Adulto Jovem
5.
Rev Alerg Mex ; 49(3): 95-8, 2002.
Artigo em Espanhol | MEDLINE | ID: mdl-12190005

RESUMO

The aspiration of foreign bodies into the airway is a common problem in childhood, mainly in children younger than 10-years old. Foreign bodies located in the tracheobronchial tree can cause episodic cough, dyspnea and wheezing, and generate a misdiagnosed of asthma if physicians do not consider the possibility of a bronchial foreign body as a differential diagnosis of this disease. In these cases, chest X-ray films are very important because those can show the most of foreign bodies or indirect radiographic signs of a bronchial foreign body. Nowadays, bronchoscopy is the method of choice for removal foreign bodies from the tracheobronchial tree. If there are not complications, most of patients may recover and become non-symptomatic in a short-term after the foreign body extraction. We show the case of a nine years old boy who suffered the aspiration of a tack, which stayed in a bronchi during several years, and was misdiagnosed as asthmatic.


Assuntos
Asma/diagnóstico , Brônquios , Erros de Diagnóstico , Corpos Estranhos/diagnóstico , Albuterol/uso terapêutico , Antiasmáticos/uso terapêutico , Antibacterianos/uso terapêutico , Broncoscopia , Criança , Tosse/etiologia , Diagnóstico Diferencial , Dispneia/etiologia , Expectorantes/uso terapêutico , Febre/etiologia , Corpos Estranhos/complicações , Corpos Estranhos/diagnóstico por imagem , Corpos Estranhos/terapia , Humanos , Masculino , Atelectasia Pulmonar/etiologia , Radiografia , Sons Respiratórios/etiologia , Sinusite/complicações
6.
Alergia (Méx.) ; 43(n.esp): 16-8, 1996.
Artigo em Espanhol | LILACS | ID: lil-181600

RESUMO

La rinosinusitis crónica afecta al 5 por ciento de la población que sufre infecciones de las vías respiratorias. El objetivo del presente estudio es conocer los sintomas predominantes en la población menor de 14 años con diagnóstico de rinosinusitis crónica, conocer su distribución etaria, por sexo y tiempo de evolución. Se incluyeron 100 pacientes con este diagnóstico a quienes se les realizaron: historia clínica, examen físico, citología nasal, pruebas cutáneas y serie de senos paranasales. Los sintomas predominantes fueron: tos, halitosis, descarga retronasal purulenta, fiebre, cefalea, odinofagia, dolor facial, y edema periorbitario, de predominio en el sexo masculino y con un tiempo promedio de evolución de 1-2 años


Assuntos
Humanos , Masculino , Feminino , Lactente , Pré-Escolar , Adolescente , Diagnóstico Clínico , Hipersensibilidade/prevenção & controle , Hipersensibilidade/terapia , Seios Paranasais , Rinite/prevenção & controle , Rinite/terapia , Sinais e Sintomas Respiratórios
7.
Alergia (Méx.) ; 34(3): 75-8, jul.-sept. 1987. tab
Artigo em Espanhol | LILACS | ID: lil-48008

RESUMO

En el presente estudio se trata de demostrar si hay correlación entre elevación de IgE, eosinofilia y parasitosis, ya que la cuantificación de la IgE es difícil y costosa, mientras que el estudio de eosinófilos es simple y económico. Los resultados muestran en forma estadística, moderada correlación entre los valores de IgE y eosinófilos. Además se encontró que en la población económicamente baja la IgE y los eosinófilos son más elevados que los de la población de estrato medio, esto pudiera explicarse por la presencia de parasitosis intestinal


Assuntos
Pré-Escolar , Criança , Humanos , Masculino , Feminino , Eosinofilia/sangue , Fezes/parasitologia , Imunoglobulina E/análise , Ensaio de Imunoadsorção Enzimática , Hipersensibilidade/diagnóstico
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA