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1.
J Perinatol ; 32(7): 559-62, 2012 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-22739841

RESUMO

Congenital cytomegalovirus (CMV) is frequently associated with active retinitis. In contrast, in the immunocompetent neonate with postnatally acquired CMV infection retinitis is rarely present and usually does not progress. We describe the case of an infant with postnatal CMV infection and active retinitis diagnosed at 20 days of life. Owing to the rapid progression of the retinitis, therapy with intravenous ganciclovir was performed, with prompt regression of the retinitis. Therapy was then continued with oral valganciclovir for one further week. Although very unusual, CMV retinitis has to be taken into consideration in neonates with early postnatally acquired CMV infection, as an early diagnosis and treatment may be crucial to avoid visual impairment.


Assuntos
Retinite por Citomegalovirus/diagnóstico , Antivirais/administração & dosagem , Retinite por Citomegalovirus/tratamento farmacológico , Ganciclovir/administração & dosagem , Humanos , Recém-Nascido , Infusões Intravenosas , Masculino
2.
Int J Pediatr Otorhinolaryngol ; 73(9): 1308-10, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-19540602

RESUMO

Heterotopic neuroglial tissue is a rare lesion, occurring more frequently in the nasal cavities. Other rare locations are the orbit, the scalp, the palate, the pharynx, the parapharyngeal space and the lungs. They are usually detected occasionally because they are often asymptomatic, but sometimes they might present with dyspnoea, feeding difficulty, snorting and nasal flaring. Respiratory symptoms occur when heterotopic neuroglial tissue is located in the parapharyngeal space. We report a case of an infant affected by Pierre Robin sequence (PRS) who was admitted to our Institution for a worsening respiratory distress that was not explainable only by PRS.


Assuntos
Coristoma/diagnóstico , Neuroglia/patologia , Faringe/patologia , Síndrome de Pierre Robin/diagnóstico , Síndrome do Desconforto Respiratório do Recém-Nascido/diagnóstico , Coristoma/complicações , Coristoma/cirurgia , Humanos , Recém-Nascido , Imageamento por Ressonância Magnética , Masculino , Faringe/cirurgia , Síndrome de Pierre Robin/complicações , Síndrome do Desconforto Respiratório do Recém-Nascido/etiologia , Síndrome do Desconforto Respiratório do Recém-Nascido/cirurgia
3.
Am J Trop Med Hyg ; 65(3): 219-26, 2001 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11561708

RESUMO

The Triatoma infestans salivary gland proteins (TSGP) can induce local and systemic hypersensitivity reactions in humans. IgG antibodies against TSGP were present in higher levels in sera of Chagas disease patients, and in individuals living in triatomine-infested areas than in controls living in triatomine-free areas. TSGP-specific IgG1 was found in sera of Chagas patients, and of individuals living in triatomine-infested rural areas, and uniquely specific IgG4 was present in sera of Chagas patients living in triatomine-infested areas, reactive against TSGP. Unique specificities were not detected in sera of individuals reacting against the ubiquitous mosquito Culex quinquifasciatus saliva proteins (CSGP). In conclusion, IgG1 reactive against TSGP is the main antibody present in individuals living in the triatomine-infested study areas. Also, IgG4 is found in the sera of insect-transmitted Chagas disease patients living in study areas.


Assuntos
Doença de Chagas/imunologia , Imunoglobulina G/imunologia , Proteínas de Insetos/imunologia , Glândulas Salivares/imunologia , Triatoma/imunologia , Animais , Western Blotting , Brasil , Doença de Chagas/sangue , Estudos de Coortes , Culex/imunologia , Feminino , Humanos , Imunoglobulina G/sangue , Imunoglobulina G/classificação , Masculino , População Rural , População Urbana
4.
J Endocrinol Invest ; 24(6): 438-44, 2001 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-11434668

RESUMO

The current study was designed to examine the relationship between body fat distribution, as evaluated by anthropometry and magnetic resonance imaging (MRI), and circulating insulin, sex hormone and SHBG levels in obese adolescent girls. Twenty-nine obese adolescent girls, aged 12.6-16.9 years with a mean BMI of 30.51+/-1.86 participated in this study. All girls had breast stage B4-5 and pubic hair stage P4-5. Percent obesity and BMI as indices of being overweight were calculated; the waist-to-hip ratio (WHR) and the waist-to-thigh ratio (WTR) were calculated to obtain two anthropometric indices for the pattern of body fat distribution. The areas of visceral (VAT) and subcutaneous adipose tissue (SAT) were evaluated by MRI at the L4-L5 level. Serum concentrations of total T, DHEAS, 17beta-estradiol, progesterone and SHBG were measured. Plasma glucose and insulin concentrations were evaluated during an oral glucose tolerance test. WHR was the only anthropometric parameter that was significantly associated with the area of VAT. Insulin level showed correlation with both WHR and the area of VAT; no correlation was found between insulin levels and WTR. Both WHR and VAT were negatively correlated with serum DHEAS level and positively correlated with T level. There were strong negative correlations between serum SHBG level and the area of VAT and WHR. Inverse correlation was found between serum SHBG level and insulin. Serum 17beta-estradiol and progesterone levels showed no significant correlation with all the patterns of body fat distribution. SAT was not significantly correlated with both anthropometric parameters and any of the sex hormones evaluated. We can draw two main conclusions. Firstly, in massively obese adolescent girls, the WHR seems to be a good indicator for the accumulation of VAT, and abdominal obesity, rather than adiposity per se, appears to be related to biochemical complications. Secondly, increased upper body adiposity and, in particular, the intra-abdominal fat area are associated with increased insulin levels in massively obese adolescent girls. The associated reductions in SHBG and DHEAS levels represent an early general risk factor for the development of metabolic and cardiovascular diseases in this population, as previously described for obese adult women.


Assuntos
Tecido Adiposo/fisiopatologia , Composição Corporal , Insulina/sangue , Obesidade/fisiopatologia , Tecido Adiposo/patologia , Adolescente , Glicemia/análise , Constituição Corporal , Criança , Sulfato de Desidroepiandrosterona/sangue , Estradiol/sangue , Feminino , Teste de Tolerância a Glucose , Humanos , Imageamento por Ressonância Magnética , Obesidade/patologia , Puberdade , Globulina de Ligação a Hormônio Sexual/análise , Testosterona/sangue , Vísceras
5.
Mem Inst Oswaldo Cruz ; 95 Suppl 1: 123-31, 2000.
Artigo em Inglês | MEDLINE | ID: mdl-11142701

RESUMO

The development of biotechnology in the last three decades has generated the feeling that the newest scientific achievements will deliver high standard quality of life through abundance of food and means for successfully combating diseases. Where the new biotechnologies give access to genetic information, there is a common belief that physiological and pathological processes result from subtle modifications of gene expression. Trustfully, modern genetics has produced genetic maps, physical maps and complete nucleotide sequences from 141 viruses, 51 organelles, two eubacteria, one archeon and one eukaryote (Saccharomices cerevisiae). In addition, during the Centennial Commemoration of the Oswaldo Cruz Institute the nearly complete human genome map was proudly announced, whereas the latest Brazilian key stone contribution to science was the publication of the Shillela fastidiosa genomic sequence highlythed on a Nature cover issue. There exists a belief among the populace that further scientific accomplishments will rapidly lead to new drugs and methodological approaches to cure genetic diseases and other incurable ailments. Yet, much evidence has been accumulated, showing that a large information gap exists between the knowledge of genome sequence and our knowledge of genome function. Now that many genome maps are available, people wish to know what are we going to do with them. Certainly, all these scientific accomplishments will shed light on many more secrets of life. Nevertheless, parsimony in the weekly announcements of promising scientific achievements is necessary. We also need many more creative experimental biologists to discover new, as yet un-envisaged biotechnological approaches, and the basic resource needed for carrying out mile stone research necessary for leading us to that "promised land" often proclaimed by the mass media.


Assuntos
Biotecnologia/tendências , Genoma de Protozoário , Interações Hospedeiro-Parasita/genética , Doenças Parasitárias/genética , Pesquisa/tendências , Animais , Mapeamento Cromossômico , Genoma , Humanos
6.
Mem Inst Oswaldo Cruz ; 91(4): 491-8, 1996.
Artigo em Inglês | MEDLINE | ID: mdl-9070409

RESUMO

The parotid lymph nodes of naive and previously infected Balb/c mice were studied after, respectively, infection and re-infection with cercariae of Schistosoma mansoni via the ears. Schistosomula were able to pass through the lymph node by following the lymph flow or by penetrating the veins of the medullary cords. The number of nodal mast cells was higher from day 2 to 6 of primary infection; and from day 5 to 11 of re-infection. The amount of degranulating mast cells was significantly higher at day 4 of infection and at day 1 of re-infection. Eosinophils characterized the nodal inflammatory processes observed after day 5 in both primarily-infected and re-infected mice. However, only in the latter the eosinophils were able to adhere to the larval surface. In primarily-infected mice, no intranodal larva presented signs of degeneration. In contrast, in re-infected animals, some degenerating larvae were found inside eosinophilic infiltrates. The eosinophils reached the nodal tissue by migrating through the high endothelial venules and their collecting veins.


Assuntos
Linfonodos/imunologia , Glândula Parótida/imunologia , Schistosoma mansoni/imunologia , Esquistossomose/imunologia , Animais , Contagem de Células , Eosinófilos/imunologia , Imunidade Celular , Linfonodos/parasitologia , Linfonodos/patologia , Masculino , Mastócitos/imunologia , Camundongos , Camundongos Endogâmicos BALB C , Glândula Parótida/parasitologia , Glândula Parótida/patologia , Esquistossomose/parasitologia
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