1000 resultados para História da medicina tropical


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El desarrollo de equipos ultrasonográficos portátiles ha permitido incorporar esta técnica a los métodos de detección precoz de la Hidatidosis Humana. En esta experiência fueron efectuadas 690 ecografias, hallándose un 5.51% de imágenes compatibles en población general y un 12.24% en grupos de riesgo (convivientes de casos operados). Se observo una disminución significativa de los porcentajes de infección en el hombre en población general en Ias áreas bajo programa de control, utilizándose Ias encuestas ecográficas para esta determinación. Se concluyó sobre la posibilidad de incorporar la ecografía a los sistemas de vigilância epidemiológica de la hidatidosis humana.

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Os autores descrevem a ocorrência de epidemias causadas pelo vírus Oropouche (ORO) nos Estados do Maranhão (MA) e Goiás (GO) em 1988. 36 amostras de vírus foram obtidas a partir da inoculação do sangue de 120 pacientes em camundongos recém nascidos. A doença foi caracterizada por febre, cefaléia, dores musculares, articulares, fotofobia, dor retro ocular, náuseas e tontura. 128 das 197 pessoas examinadas em Porto Franco, MA, tinham anticorpos inibidores da hemaglutinação (IH) para o agente e, em 106 foram detectados anticorpos IgM por MAC ELISA. Todos os grupos etários foram infectados, embora a incidência tenha sido mais elevada entre aqueles com 10 a 19 anos de idade. Quanto ao sexo, a infecção ocorreu igualmente em ambos os sexos. Recorrência dos sintomas foi observada em 56% dos casos positivos estudados. A inoculação em camundongos Swiss recém nascidos de 3.624 Culicoides paraensis (Ceratopogonidae) e 1.970 Culex (Culex) quinquefasciatus (Culicidae), coletados em Porto Franco-MA, resultou em um único isolamento do vírus ORO a partir dos Culicoides. Essa é a primeira descrição de casos confirmados de infecção pelo vírus Oropouche nos Estados do Maranhão e Goiás, Brasil.

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In search of an efficient but simple, low cost procedure for the serodiagnosis of Toxoplasmosis, especially suited for routine laboratories facing technical and budget limitations as in less developed countries, the diagnostic capability of Hematoxo® , an hemagglutination test for toxoplasmosis, was evaluated in relation to a battery of tests including IgG- and IgM-immunofluorescence tests, hemagglutination and an IgM-capture enzymatic assay. Detecting a little as 5 I.U. of IgG antitoxoplasma antibodies, Hematoxo® showed a straight agreement as to reactivity and non-reactivity for the 443 non-reactive and the 387 reactive serum samples, included in this study. In 23 cases presenting a serological pattern of acute toxoplasmosis and showing IgM antibodies, Hematoxo® could detect IgM antibodies in 18, indicated by negativation or a significant decrease in titers as a result of treating samples with 2-mercapto-ethanol. However, a neat increase in sensitivity for IgM specific antibodies could be achieved by previously removing IgG from the sample, as demonstrated in a series of acute toxoplasmosis sera. A simple procedure was developed for this purpose, by reconstituting a lyophilized suspension of Protein A - rich Staphylococcus with the lowest serum dilution to be tested. Of low cost and easy to perform, Hematoxo® affords not only a practical qualitative procedure for screening reactors and non-reactors, as in prenatal services, but also quantitative assays that permit to titrate antibodies as well as to identify IgM antibodies.

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This report describes the first documented case of Erysipelothrix rhusiopathiae endocarditis in Latin America. The patient was a 51-years-old male, moderate alcoholic, with a previous history of aortic failure. He was used to fishing and cooking as a hobby and had his left hand wounded by a fish-bone. The disease began with erysipeloid form and developed to septicemia and endocarditis. He was treated with antibiotics and surgery for aortic valve replacement. There are only 46 cases of E. rhusiopathiae endocarditis reported to date. The authors wonder if several other cases might go unreported for lack of microbiological laboratorial diagnosis.

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Pathogenic Yersinia pestis isolates were collected during a plague outbreak at the Paraiba State in 1986. The Y. pestis isolates were investigated for the presence of virulence-associated factors and plasmid content. All strains analysed were proficient in the expression of the VW and fraction 1 antigens, pigment adsorption and pesticin-fibronolysin-coagulase production. A similar plasmid profile composed by four plasmid with molecular weight of 60, 44, 14.9, and 6.4 Megadaltons (MD) was found in all strains. DNA cleavage with EcoRI restriction enzyme further demonstrated the uniform plasmid content of the Y. pestis isolates. Seven additional Y. pestis strains, previously isolated in the same region but in an endemic state, showed the same plasmid fingerprint. The lack of any detectable difference between epidemic and endemic isolates as well as the value of plasmid fingerprints in epidemiology of Y. pestis is discussed.

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O tratamento etiológico da doença de Chagas é iniciado geralmente apenas quando se dispõe de um diagnóstico parasitológico positivo. Na tentativa de aumentar o número de candidatos assim selecionados para o tratamento específico, estudamos 36 pacientes chagásicos crônicos associando o xenodiagnóstico, a hemocultura e o teste de lise mediada pelo complemento, em duas séries sucessivas, intercaladas de um mínimo de 60 dias. A sensibilidade do xenodiagnóstico e da hemocultura foi respectivamente de 30,5% e de 8,3% na primeira série e de 36,1% e de 19,4% nas duas séries. Foram positivos, em pelo menos uma das duas provas, 17 (47,2%) dos pacientes. Destes, entretanto, somente 9 (53,0%) mostraram teste de lise constantemente positivo enquanto que em 5 (29,4%) o teste foi negativo e 3 (17,6%) apresentaram resultados ora positivos, ora negativos. Nos pacientes com provas parasitológicas negativas, o teste de lise foi positivo em 4 (15,8%), negativo em 9 (47,4%) e discordante em 6 (31,5%). Assim, o teste de lise mediada pelo complemento não se constitue em bom método de triagem de candidatos ao tratamento. Apesar da baixa sensibilidade, as provas parasitológicas ainda constituem o instrumento mais seguro para o clínico.

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El objetivo del trabajo fue lograr la reproducción experimental del ciclo evolutivo de Diphyllobothrium erinaceieuropei Rudolphi 1819 (Cestoda, Pseudophyllidea) con la intervención de Paracyclops fimbriatus y larvas de Bufo arenarum como hospedadores intermediarios y caninos como hospedadores definitivos. Los huevos del parásito se obtuvieron de heces de caninos infectados naturalmente y se conservaron refrigerados en agua. Se incubaron 7 días a 25°C para que desarrollaran los coracidios y se pusieron en recipientes que contenían a los copépodos mencionados. Al cabo de 12 días a 22,6°C (promedio) se hallaron procercoides maduros en ellos y se agregaron 10 renacuajos de Bufo arenarum. Estos se examinaron por disección 22, 23, 61 y 107 días después, hallándose en todos 1 o más plerocercoides (Temperatura promedio: 24,9°C). El día 23, de 6 renacuajos se obtuvieron 49 plerocercoides, de los cuales se administraron 28, por vía oral, a una perra. El día 107, 3 de 11 plerocercoides obtenidos de un renacuajo se le dieron a otra perra por la misma vía. Se hallaron huevos del cestode en las heces del primer canino a partir del día 22 posterior a la infección (p.i.) y a los 30 días p.i., segmentos de estróbila. En el segundo canino se hallaron huevos a los 30 días p.i..

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Foi estudada a migração do Schistosoma mansoni (cepas LE e SJ) em oito grupos de camundongos albinos (Mus musculus) não isogênicos, infectados transcutaneamente com cerca de 450 cercarias não irradiadas (grupos controles) e irradiadas com 3 Krad, 20 Krad e 40 Krad de radiação gama proveniente de cobalto-60, Na pele, observou-se uma diminuição progressiva das taxas de recuperação em função do tempo e, nos pulmões e sistema porta, verificou-se uma relação inversa significativa entre as taxas de recuperação total e as doses de irradiação. A dose de 20 Krad praticamente impede a migração dos parasites, de ambas as cepas, dos pulmões até o sistema porta, enquanto a de 40 Krad praticamente impede a migração dos mesmos da pele para os pulmões.

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The authors compare the serologic efficacy and the clinical protection afforded by three different measles vaccination schemes in adequately nourished children in São Paulo city, Brazil. Two hundred forty two children were divided into three groups. Group A, comprising 117 children who had received the vaccine before 12 months of age and a second dose at 12 months of age or more. Group B, comprising 46 children who had received only one dose, before 12 months of age. Group C, comprising 79 children who had received only one dose, at 12 months of age or more. The geometric mean titer of antibodies in Group A was 790.1; in Group B, 251.1; and in Group C, 550.3. There was no statistically significant difference between Groups A and C. The exposure to the measles virus was probably similar in all groups, and the children in Groups A and C had similar chances of acquiring the disease after vaccination whereas in Group B the chances were higher when compared to the other two groups. The results obtained in this study favor the use, in developing countries, of a vaccination program against measles that includes an early first dose at eight months of age and revaccination after 12 months of age.

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The detection of HBV-DNA in serum by molecular hybridization is the most sensitive and specific marker of replication and infectivity of hepatitis B virus and currently is proposed as a routine diagnostic technique in the follow-up of HBV - related diseases. Comparing different techniques already described, we found that direct spotting of serum samples on nitrocellulose membranes under vacuum filtration, followed by denaturing and neutralizing washes is more practical, simple, sensible and reproducible. DNA polymerase assay using phosphonoformic acid as specific viral inhibitor has shown 86.8% of concordance with HBV-DNA detection, and so, it is an useful alternative in the follow-up of hepatitis B chronic patients. We found 19.2% HBeAg positive samples with no other markers of viral replication and no anti-HBe positive sample had detectable HBV-DNA. Discordance between the 2 systems have been extensively described, and we confirm this for the first time in our country. Molecular biological techniques are essential to determine the replication status of chronic hepatitis B patients.

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In order to define an accurate assay for anti-adenovirus antibody detection, a recently developed ELISA was compared with IFA and CF. On 58 sera, the ELISA was more sensitive than both CF and IFA, which showed relative sensitivities of 63% and 94%, respectively. It was not possible to determine the exact specificity of the tests because of the lack of a gold standard. Furthermore, the ELISA was used to define the prevalence of adenovirus antibodies in 116 infants between 1 and 24 months old (mean 7.28). The data showed that maternal antibodies waned by the age of 5 to 6 months and that more than 80% of the children had been infected by adenoviruses by the age of 10 months.

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In the present work the immune adherence hemagglutination test (IAHA) was standardized in a simplified procedure. This test showed good reproducibility, better than the classical mice serum neutralization test (SN). The tests showed high correlation degree: high titers in one test corresponded to high titers in the other one, and the same occured with low titers. The IAHA test is extremely simple, fast to perform, and of low cost when compared to tests such as SN or indirect immunofluorescense (IIF). It also proved to be useful in less sophisticated laboratories or even as a screening test for the titration of rabies antibodies.

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Se estudió la susceptibilidad "in vitro" de 24 cepas de 3 especies del género Cryptococcus a 5 drogas antifúngicas (anfotericina B, 5 fluorocitosina, ketoconazol, itraconazol y miconazol). Las mismas se agruparon según su especie, variedad y origen de aislamiento. Para determinar la concentración inhibitoria mínima (C.I.M.) de cada droga se empleó el método de dilución en agar con el medio básico nitrogenado para levaduras, adicionado de glucosa. Se obtuvo además la media geométrica de estos valores para cada grupo y se comparó cada uno de ellos. Los resultados obtenidos fueron homogéneos con la sola excepción de las cepas de Cryptococcus sp (no neoformans), en las cuales se detectaron elevados valores de C.I.M. para la 5 fluorocitosina.

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La esporotricosis consiste en micosis profunda, de evolución subaguda o crónica decurrente de infección por el hongo dimorfico Sporothrix schenkii. Consiste en dermatopatia mucho frecuente en nuestro medio, resultante de la penetración de abrojos e de arañazos por espinos de plantas. El S. schenkii ha sido descrito, en S. Paulo, en perros, gatos, aseninos, bovinos, equinos y ratones. Todavía, el carácter de antropozoonosis de la enfermedad pocas veces ha sido descrito tanto en la literatura internacional como en la nacional, existiendo apenas una citación en lo Brasil, de probable transmisión gato/hombre. Se discrebió, en lo presente relato, caso clínico de esporotricosis felina con transmisión através de arañadura en propietario, tratador y médico veterinário. Un gato, sin raza definida, macho, con 3 años, mucho agresivo, con grave cuadro cutáneo (cefálico, torácico y de miembros torácicos) manifestado por lesiones ulceradas, exudativas de alopecia, deposición de crostas hemorrágicas, agraviado por síntomas de lo complejo respiratorio felino, donde por su temperamento agresivo habia arenado en corto espacio de tiempo 5 individuos, donde 3 de los individuos manifestaron sintomas de evolución y gravedad distintas. El diagnostico clínico presuntivo fue confirmado perlo examen histopatológico (H.E., PAS) de fragmentos de piel, linfonodos y amígdalas cogidos, "intra-vitam" y/o "post-morten", per lo aislamiento de lo agente, per la inoculación en testículos de ratas adultas y posterior nuevo aislamiento. Se confirmó la patologia por pruebas suerológicas (F.C., anticuerpos precipitantes) y prueba de intradermoreación (esporotriquina) en los pacientes acometidos.