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1.
Braz J Med Biol Res ; 49(12): e5519, 2016 Dec 12.
Artigo em Inglês | MEDLINE | ID: mdl-27982280

RESUMO

The presence of the single nucleotide polymorphisms in exon 1 of the mannose-binding lectin 2 (MBL2) gene was evaluated in a sample of 159 patients undergoing coronary artery bypass surgery (71 patients undergoing valve replacement surgery and 300 control subjects) to investigate a possible association between polymorphisms and heart disease with Chlamydia infection. The identification of the alleles B and D was performed using real time polymerase chain reaction (PCR) and of the allele C was accomplished through PCR assays followed by digestion with the restriction enzyme. The comparative analysis of allelic and genotypic frequencies between the three groups did not reveal any significant difference, even when related to previous Chlamydia infection. Variations in the MBL plasma levels were influenced by the presence of polymorphisms, being significantly higher in the group of cardiac patients, but without representing a risk for the disease. The results showed that despite MBL2 gene polymorphisms being associated with the protein plasma levels, the polymorphisms were not enough to predict the development of heart disease, regardless of infection with both species of Chlamydia.


Assuntos
Infecções por Chlamydia/sangue , Infecções por Chlamydia/genética , Doenças das Valvas Cardíacas/microbiologia , Lectina de Ligação a Manose/sangue , Lectina de Ligação a Manose/genética , Estudos de Casos e Controles , Infecções por Chlamydia/diagnóstico , Estudos Transversais , Feminino , Frequência do Gene , Predisposição Genética para Doença , Genótipo , Doenças das Valvas Cardíacas/sangue , Doenças das Valvas Cardíacas/cirurgia , Humanos , Masculino , Pessoa de Meia-Idade , Reação em Cadeia da Polimerase , Polimorfismo de Nucleotídeo Único
2.
Braz. j. med. biol. res ; 49(12): e5519, 2016. tab, graf
Artigo em Inglês | LILACS | ID: biblio-828177

RESUMO

The presence of the single nucleotide polymorphisms in exon 1 of the mannose-binding lectin 2 (MBL2) gene was evaluated in a sample of 159 patients undergoing coronary artery bypass surgery (71 patients undergoing valve replacement surgery and 300 control subjects) to investigate a possible association between polymorphisms and heart disease with Chlamydia infection. The identification of the alleles B and D was performed using real time polymerase chain reaction (PCR) and of the allele C was accomplished through PCR assays followed by digestion with the restriction enzyme. The comparative analysis of allelic and genotypic frequencies between the three groups did not reveal any significant difference, even when related to previous Chlamydia infection. Variations in the MBL plasma levels were influenced by the presence of polymorphisms, being significantly higher in the group of cardiac patients, but without representing a risk for the disease. The results showed that despite MBL2 gene polymorphisms being associated with the protein plasma levels, the polymorphisms were not enough to predict the development of heart disease, regardless of infection with both species of Chlamydia.


Assuntos
Humanos , Masculino , Feminino , Pessoa de Meia-Idade , Infecções por Chlamydia/sangue , Infecções por Chlamydia/genética , Doenças das Valvas Cardíacas/microbiologia , Lectina de Ligação a Manose/sangue , Lectina de Ligação a Manose/genética , Estudos de Casos e Controles , Infecções por Chlamydia/diagnóstico , Estudos Transversais , Frequência do Gene , Predisposição Genética para Doença , Genótipo , Doenças das Valvas Cardíacas/sangue , Doenças das Valvas Cardíacas/cirurgia , Reação em Cadeia da Polimerase , Polimorfismo de Nucleotídeo Único
3.
Am J Transplant ; 14(1): 96-101, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-24369026

RESUMO

Visceral leishmaniasis is an uncommon disease in transplant recipients; however, if left untreated, the mortality can be high. If an organ donor or recipient is known to be an asymptomatic Leishmania spp. carrier,monitoring is advised. This study proposes to assess the prevalence of asymptomatic Leishmania spp.infection in liver transplant donors and recipients from an endemic area. A total of 50 liver recipients and 17 liver donors were evaluated by direct parasite search, indirect fluorescent antibody test (IFAT), anti-Leishmania rK39 rapid test and Leishmania spp.DNA detection by polymerase chain reaction (PCR).Leishmania spp. amastigotes were not observed in liver or spleen tissues. Of the 67 serum samples, IFAT was reactive in 1.5% and indeterminate for 17.9%, and the anti-Leishmania rK39 rapid test was negative for all samples. The PCR test was positive for 7.5%, 8.9%, and 5.9% of blood, liver and spleen samples, respectively(accounting for 23.5% of the donors and 8% of the recipients). Leishmania infantum-specific PCR confirmed all positive samples. In conclusion, a high prevalence of asymptomatic L. infantum was observed in donors and recipients from an endemic area, and PCR was the most sensitive method for screening these individuals.


Assuntos
Leishmaniose Visceral/epidemiologia , Transplante de Fígado/efeitos adversos , Adolescente , Adulto , Idoso , Brasil/epidemiologia , Criança , Pré-Escolar , Estudos Transversais , DNA de Protozoário/análise , Feminino , Imunofluorescência , Humanos , Leishmania/genética , Leishmania infantum/imunologia , Leishmaniose Visceral/diagnóstico , Masculino , Pessoa de Meia-Idade , Reação em Cadeia da Polimerase , Prevalência , Estudos Prospectivos , Doadores de Tecidos
4.
Transplant Proc ; 45(1): 297-300, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23375318

RESUMO

The Model for End-Stage Liver Disease (MELD), which predicts mortality on the waiting list before liver transplantation, has changed organ allocation criteria to prioritize severely ill patients. The aim of this study was to investigate the impact of the new criteria on the incidence of Healthcare Associated Infections (HAI) and patient survival after liver transplantation. This retrospective cohort included liver transplant recipients from 2005 to 2007. Infection notification followed the recommended criteria of the National Healthcare Safety Network (NHSN). Statistical analysis was performed using the Statistical Package for the Social Sciences. Of 142 patients, 67 (47.2%) underwent transplantation before June 2006. There were no differences between the 2 periods considering patient gender, diagnosis, age, length of hospitalization, and mean time to first infection occurrence. However, the length of intensive care unit (ICU) hospitalization (P = .006) and central venous catheter (CVC) use (P = .025) were higher in the first period of the study. Comparison of time until first systemic infection before and after changes in allocation criteria showed no significant difference (log-rank = 0.06; P = .81). There was a trend toward greater lethality during the second period of the study (P = .09). There was no difference in time to death between the 2 periods (log-rank = 0.9; P = .76). However, when comparing time to death of all patients with systemic infection versus those without this event, patients without infection showed a higher mortality rate (log-rank = 15.7; P < .001).


Assuntos
Doença Hepática Terminal/patologia , Doença Hepática Terminal/terapia , Falência Hepática/cirurgia , Transplante de Fígado/métodos , Obtenção de Tecidos e Órgãos/métodos , Listas de Espera , Adolescente , Adulto , Idoso , Algoritmos , Brasil , Estudos de Coortes , Doenças Transmissíveis/complicações , Doenças Transmissíveis/terapia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Modelos Estatísticos , Fatores de Tempo , Resultado do Tratamento , Adulto Jovem
5.
Genet Mol Res ; 11(2): 1272-9, 2012 May 14.
Artigo em Inglês | MEDLINE | ID: mdl-22614356

RESUMO

Planting resistant varieties is the most effective control measure against the angular leaf spot of dry beans, a fungal disease caused by Pseudocercospora griseola. However, dry bean varieties with durable resistance are not easily obtained. Knowledge about the genetic variability of the pathogen population is key for the success of dry bean breeding programs aimed at developing resistant materials, but finding suitable operationally simple and genetically accurate markers is not an easy task. The aim of this study was to assess the suitability of the ISSR-PCR technique to quantify the genetic variability of P. griseola isolates. Total DNA of 27 P. griseola isolates from Goiás, Minas Gerais, Espírito Santo, and Paraná States was extracted and amplified using specific primers for ISSR. Using cluster analysis, 27 genotypes were identified. The ISSR-PCR technique was suitable for assessing intraspecific variability of P. griseola. The ISSR-PCR marker was found to be highly sensitive to genetic variation and can aid in elucidating the genetic structure of the population of this plant pathogen as a support tool for the dry bean breeding programs.


Assuntos
Ascomicetos/genética , Variação Genética , Ascomicetos/isolamento & purificação , Sequência de Bases , Brasil , Análise por Conglomerados , Primers do DNA , Reação em Cadeia da Polimerase
6.
Genet Mol Res ; 10(4): 3552-8, 2011 Dec 14.
Artigo em Inglês | MEDLINE | ID: mdl-22194206

RESUMO

Polymorphisms in the TP53 gene codon 72 (Arg72Pro) influence apoptosis induction and DNA damage repair. We evaluated how variants of protein p53 (p53Arg and p53Pro) affect cell death and DNA damage repair by analyzing the frequencies of karyorrhexis and micronuclei. There were significant differences in the frequency of karyorrhexis between the three p53 genotypes (Arg/Arg, Arg/Pro, and Pro/Pro), between samples taken before and after radiotherapy, and between patients and controls. The frequency of micronucleated cells increased significantly after radiotherapy. There were no significant differences in the micronucleus frequency in healthy tissues of these patients compared to controls, or in the comparisons between the three genotypes. We conclude that Arg72Pro polymorphism influences cell apoptotic capacity. This is the first study investigating karyorrhexis and micronuclei, as indicators of apoptosis after radiotherapy, and how these indicators are influenced by the TP53 polymorphism Arg72Pro.


Assuntos
Substituição de Aminoácidos/genética , Predisposição Genética para Doença , Mucosa Bucal/patologia , Mucosa Bucal/efeitos da radiação , Polimorfismo de Nucleotídeo Único/genética , Radioterapia , Proteína Supressora de Tumor p53/genética , Adulto , Idoso , Idoso de 80 Anos ou mais , Estudos de Casos e Controles , Frequência do Gene/genética , Mutação em Linhagem Germinativa/genética , Humanos , Micronúcleos com Defeito Cromossômico , Pessoa de Meia-Idade
7.
Braz J Infect Dis ; 14(1): 54-9, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20428655

RESUMO

Methicillin-resistant Staphylococcus aureus (MRSA) infections frequently complicate the post-operative course of transplant recipients, and despite nasal carriage and endemic colonization, MRSA outbreaks are not commonly described. This study reports a case of MRSA outbreak and discusses infection control measures and recommendations for this situation.


Assuntos
Infecção Hospitalar/epidemiologia , Surtos de Doenças , Staphylococcus aureus Resistente à Meticilina/isolamento & purificação , Infecções Estafilocócicas/epidemiologia , Transplante , Transplante de Medula Óssea/estatística & dados numéricos , Infecção Hospitalar/microbiologia , Genótipo , Humanos , Transplante de Rim/estatística & dados numéricos , Transplante de Fígado/estatística & dados numéricos , Fenótipo , Estudos Prospectivos , Fatores de Risco , Infecções Estafilocócicas/microbiologia , Transplante/estatística & dados numéricos
8.
Rev. bras. plantas med ; 12(1): 73-79, jan.-mar. 2010. ilus, tab
Artigo em Inglês | LILACS | ID: lil-578937

RESUMO

A nodal segment culture was developed in order to assess Solanum torvum Sw. regeneration and solasodine levels. The influence of auxins (indoleacetic acid, 1-Naphthaleneacetic acid) and benzyl adenine on S. torvum growth in micropropagation was investigated. A nodal segment culture was initiated with seeds germinated in MS basal medium added of GA3 and grown in different concentrations of IAA, IAA + BAP and NAA + BAP. Sixty-day-old plants from the in vitro culture were collected, frozen and lyophilized; then, the methyl orange method was used to quantify solasodine for the spectrophotometric assay. The best results regarding plant regeneration and solasodine accumulation were obtained by using the MS basal medium without addition of plant growth regulators; however, there was great production of calluses presenting friable bases. Based on these results, cell cultures can be initiated from such calluses with application of other auxins and cytokinins to enhance solasodine production, besides different elicitors, light intensities and sucrose concentrations.


A regeneração de Solanum torvum e a avaliação do conteúdo de solasodina foram os objetivos de cultura de segmentos nodais. A influência de auxinas (ácido 3-indolacético, ácido naftalenoacético) e de 6-benzilaminopurina no crescimento de S. torvum na micropropagação foi investigado. Cultura de segmentos nodais foi iniciada por sementes germinadas em meio básico MS acrescido de GA3 e cultivadas em diferentes concentrações de AIA, AIA + BAP e ANA + BAP. Plantas da cultura in vitro com 60 dias foram coletadas, congeladas e liofilizadas e o método de alaranjado de metila foi utilizado para quantificação de solasodina para o ensaio espectrofotométrico. Os melhores resultados para regeneração vegetal e acúmulo de solasodina foram alcançados no meio MS sem adição de reguladores de crescimento havendo, porém grande produção de calos de base friáveis. Esses resultados mostram que a partir desses calos, cultura de células pode ser iniciada com aplicação de outras auxinas e citocininas para o aumento da produção de solasodina além de diferentes eliciadores, intensidades luminosas e concentrações de sacarose.


Assuntos
Alcaloides de Solanáceas/química , Solanaceae/crescimento & desenvolvimento , Álcalis , Citocininas , Fenômenos Fisiológicos Vegetais/fisiologia , Esteroides
9.
Nutr Neurosci ; 13(1): 21-8, 2010 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-20132651

RESUMO

Perinatal nutrition has persistent influences on neural development and cognition. In humans and other animals, protein malnutrition during the perinatal period causes permanent changes, inducing to adulthood metabolic syndrome. Feeding is mainly modulated by neural and hormonal inputs to the hypothalamus. Hypothalamic glycogen stores are a source of glucose in high energetic demands, as during development of neural circuits. As some hypothalamic circuits are formed during lactation, we studied the effects of malnutrition, during the first 10 days of lactation, on glycogen stores in hypothalamic nuclei involved in the control of energy metabolism. Female pregnant rats were fed ad libitum with a normal protein diet (22% protein). After delivery, each dam was kept with 6 male pups. During the first 10 days of lactation, dams from the experimental group received a protein-free diet and the control group a normoprotein diet. By post-natal day 10 (P10), glycogen stores were very high in the arcuate nucleus and median eminence of control group. Glycogen stores decreased during development. In P20 control animals, glycogen stores were lower when compared to P10 control animals. Animals submitted to malnutrition presented a staining even lower than control ones. After P45, it was difficult to determine differences between control and diet groups because glycogen stores were reduced. We also showed that tanycytes were the cells presenting glycogen stores. Our data reinforce the concept that maternal nutritional state during lactation may be critical for neurodevelopment since it resulted in a low hypothalamic glycogen store, which may be critical for establishment of neuronal circuitry.


Assuntos
Animais Lactentes/metabolismo , Glicogênio/metabolismo , Hipotálamo/patologia , Deficiência de Proteína/patologia , Envelhecimento/metabolismo , Animais , Animais Lactentes/crescimento & desenvolvimento , Núcleo Arqueado do Hipotálamo/crescimento & desenvolvimento , Núcleo Arqueado do Hipotálamo/metabolismo , Núcleo Arqueado do Hipotálamo/patologia , Dieta com Restrição de Proteínas , Feminino , Proteína Glial Fibrilar Ácida , Transportador de Glucose Tipo 2/metabolismo , Hipotálamo/crescimento & desenvolvimento , Hipotálamo/metabolismo , Masculino , Fenômenos Fisiológicos da Nutrição Materna , Eminência Mediana/crescimento & desenvolvimento , Eminência Mediana/metabolismo , Eminência Mediana/patologia , Proteína Básica da Mielina/metabolismo , Neuroglia/classificação , Neuroglia/patologia , Especificidade de Órgãos , Deficiência de Proteína/metabolismo , Distribuição Aleatória , Ratos , Ratos Wistar , Fatores de Transcrição/metabolismo , Vimentina/metabolismo
11.
Transplant Proc ; 37(5): 2293-6, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15964402

RESUMO

Bone Marrow Transplant (BMT) is a lifesaving procedure for several diseases. Histocompatibility between host and donor is crucial for the success of this therapy. Since human leukocyte antigen (HLA) genes are the most polymorphic in humans, a foreknowledge of their frequencies and a vast register of volunteer donors are important for patients who need an unrelated donor. This research evaluated data from 3500 HLA-typed donors using PCR-SSP (One Lambda ABDRX kits, low/medium resolution). The allele and haplotype frequencies were calculated from the donor HLA typings. Among the total sample we observed that the allelic groups HLA-A*02, -B*35, and -DRB1*11 had frequencies of 0.228, 0.112, and 0.125, respectively. The haplotype HLA-A*01-B*08-DRB1*03 was the most frequent (0.024). We also compared our results with another study conducted in a Northeastern Brazilian population. The identification of the most common allelic groups and haplotypes is of great interest, not only to know the HLA composition of the population but also to search for the best HLA match for a transplant. However, the search for the perfect match depends on the eventual registration of every specific donor in the national registers for bone marrow donation.


Assuntos
Transplante de Medula Óssea/imunologia , Antígenos HLA/genética , Antígenos HLA/imunologia , Haplótipos , Doadores Vivos , Brasil , Antígenos HLA-B/genética , Antígenos HLA-B/imunologia , Antígenos HLA-DR/genética , Antígenos HLA-DR/imunologia , Cadeias HLA-DRB1 , Teste de Histocompatibilidade , Humanos , Reação em Cadeia da Polimerase , Polimorfismo Conformacional de Fita Simples
12.
Ann Trop Med Parasitol ; 99(3): 229-36, 2005 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15829132

RESUMO

Visceral leishmaniasis (VL) caused by Leishmania chagasi is a growing public-health problem in many parts of the New World. Although several studies have focused on the consequences of environmental damage, human migration and land occupation on the incidence of VL, the effects on the disease of the substandard living conditions that often result from the process of urbanization have not been investigated in detail. The present study was based in the Brazilian city of Teresina, where, since 1980, there have been two large outbreaks of VL (one in 1981-1985 and the other in 1993-1996), each involving at least 1000 newly reported cases. The role of household structure and the provision of urban services in the city, as predictors of the occurrence of VL, was studied in a case-control investigation. After controlling for age, crowding, and the background incidence of VL in the area where the subjects lived, the risk of acquiring the disease was found to be significantly higher for those who lived in houses with an inadequate sewage system and those who had no regular rubbish collection. Improving household structure and providing basic urban services might be effective strategies for controlling the spread of VL in urban areas.


Assuntos
Leishmania infantum , Leishmaniose Visceral/transmissão , Prática de Saúde Pública , Urbanização , Animais , Brasil , Estudos de Casos e Controles , Habitação , Humanos , Leishmaniose Visceral/prevenção & controle , Pobreza , Eliminação de Resíduos , Esgotos
13.
Interv Neuroradiol ; 11(4): 363-7, 2005 Dec 20.
Artigo em Inglês | MEDLINE | ID: mdl-20584449

RESUMO

SUMMARY: Carotid cavernous fistulas (CCF) are mostly post-traumatic and are due to a tear of the internal carotid artery (ICA) inside the cavernous sinus. The improvement of endovascular techniques with venous approach enables the preservation of internal carotid artery patency in most cases when detachable balloons fail in order to reconstruct and repair the tear in the ICA. The case described here has a giant aneurysmatic dilatation of the cavernous sinus and inferior petrosal sinus. We associate coils and Onyx to occlude the lesion preserving and repairing the large hole of the fistula.

14.
Acta Trop ; 83(1): 13-8, 2002 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-12062788

RESUMO

First noted in the city of Teresina in 1981, the last decades have witnessed a remarkable increase in urban transmission of American visceral leishmaniasis (VL) in many Brazilian cities. Teresina, the site of this study, has faced two large outbreaks of VL. The first occurred from 1981-1985 when almost 1000 new cases were reported. The second started in the 1990s, and between 1993 and 1996 more than 1200 new cases were detected. This report describes the prevalence of infection with Leishmania chagasi in Teresina at the end of the second outbreak and gives estimates of the number of people who became infected during the epidemic. Between June 1995 and May 1996, 200 households were chosen at random from a list of addresses covering about 93% of Teresina's urban households. In each household, one person over the age of 1 year was screened for Leishmania antibodies and skin-tested. Nearly 50% of persons had a positive leishmanin reaction, but only 13.9% had detectable antibodies to L. chagasi. While prevalence estimates based on the leishmanin skin-test increased with age (P<0.001), those based on serological tests showed a lesser, and non significant, variation with age (P=0.31). Using a geometric growth equation, and assuming that the annual distribution of clinical cases may serve as an approximation to what would have been the distribution of infections by year, we estimated that over 320000 persons were infected during the epidemic. Little is known about the epidemiology of VL in urban areas, where social networks, population density, and relationships of housing with the natural environment are more varied and complex than in the rural scene. In those areas, control interventions have failed to eliminate transmission of the parasite and prevent new epidemics. Further epidemiological studies of VL in urban areas might be needed to inform control actions.


Assuntos
Surtos de Doenças , Leishmaniose Visceral/epidemiologia , Adolescente , Adulto , Anticorpos Antiprotozoários/isolamento & purificação , Brasil/epidemiologia , Criança , Pré-Escolar , Humanos , Lactente , Leishmaniose Visceral/imunologia , Prevalência , Estudos Soroepidemiológicos , População Urbana
15.
Interv Neuroradiol ; 8(1): 55-60, 2002 Mar 30.
Artigo em Inglês | MEDLINE | ID: mdl-20594513

RESUMO

SUMMARY: A high flow pial arteriovenous fistula in a twenty-years-old girl is described. The arteriovenous communication corresponds to a single hole fistula on the right rolandic area, with a giant venous ectasia. The patient presented seizures and left hemiparesis as symptoms. The fistula was embolized with glue obtaining total occlusion of the shunt. Hypotension was induced and valsalva manoeuver was done during the glue injection to reduce the flow into the fistula, however 26 hours after the procedure the patient bled resulting in a fatal outcome. The purpose of this paper is discuss the presentation of Rendu-Osler-Weber (ROW) in children and the therapeutic guidelines.

16.
Interv Neuroradiol ; 7(2): 121-6, 2001 Jun 30.
Artigo em Inglês | MEDLINE | ID: mdl-20663337

RESUMO

SUMMARY: We describe a rare case of multiple arteriovenous fistulae of the spinal cord (SCAVF) in the same myelomer in a five-year-old boy. This case report consists of a trifocal SCAVF at the Th12 myelomeric level without communication between the three different fistulae. Two AVF were located posteriorly, bilateraly, in the spinal cord, fed by left and right posterior radiculopial arteries and one anteriorly in the anterior spinal axis. The venous drainage was independent for each lesion. The patient presents associated lesions characterized by cutaneous stain and inferior limb asymmetry. A metameric distribution is the explanation for the multiplicity of these lesions in a syndromic association related to Cobb syndrome. The patient was treated by transarterial embolization using glue with occlusion of the three different fistulae. The patient achieved a good improvement in neurological status.

17.
Cir. vasc. angiol ; 11(3): 55-9, set. 1995. ilus, tab
Artigo em Português | LILACS | ID: lil-165675

RESUMO

Sendo a ressonância nuclear magnética (RNM) capaz de detectar o deslocamento de sangue no sistema vascular, procurou-se avaliar sua capacidade em diagnosticar a trombose venosa profunda aguda (TVP) dos membros inferiores. Vinte e um pacientes foram submetidos ao estudo do sistema venoso profundo pelo RNM e pela flebografia radiológica convencional. Vinte desses pacientes apresentavam suspeita de TVP pelo exame clínico armado com estetoscópio Doppler ultra-som. Os resultados da RNM foram comparados m os obtidos pela flebografia convencional, considerando-se os achados em cada veia e nos andares ílio-cava, femoro-poplíteo e distal. Em veias cava, ilíaca comum e líaca externa, a sensibilidade da RNM foi de 100 por cento nso dosi primeiros e de 90 por cento no último caso. A sensibilidade no andar ílio-cava foi de 100 por cento. Em veias femoral comum, femoral profunda e poplítea, a sensibilidade foi de 79 por cento, 94 por cento e 87 por cento, respectivamente. Considerando-se o andar femoro-poplíte,a sensibilidade foi de 94 por cento. Nos três gurpos distais - tibial anterior, tibial posteiro e fibular - a sensibilidade foi de 100 por cento. A RNM é exame que permite o diagnóstico da TVP dos membros inferiores com alto grau de sensibilidade, podendo vir a se tornar um procedimento propedêutico alternativo para flebografia convencional.


Assuntos
Diagnóstico por Imagem , Espectroscopia de Ressonância Magnética , Tromboflebite
18.
Arq Neuropsiquiatr ; 45(4): 403-11, 1987 Dec.
Artigo em Português | MEDLINE | ID: mdl-3329508

RESUMO

The authors report three cases of central nervous system cryptococcosis in children in the first decade of life, from Rio Grande do Sul State, Brazil. Diagnosis was supported by demonstration of Cryptococcus neoformans with India-ink preparations of the spinal fluid and Sabouraud's media culture. Clinical presentation included acute, subacute and chronic forms. Increased intracranial pressure and hydrocephalus were the complications during the course of the disease, and a ventriculoperitoneal shunt was used in one case. Undernutrition was associated with all cases and tubercle bacillus infection with one. Specific therapy was administered to the three patients. One patient was cured and the other two died.


Assuntos
Encefalopatias/microbiologia , Criptococose , Fatores Etários , Anfotericina B/uso terapêutico , Encefalopatias/epidemiologia , Brasil , Líquido Cefalorraquidiano/microbiologia , Criança , Pré-Escolar , Criptococose/tratamento farmacológico , Criptococose/epidemiologia , Criptococose/mortalidade , Cryptococcus neoformans/isolamento & purificação , Feminino , Humanos , Masculino , Meningoencefalite/microbiologia
19.
J Clin Endocrinol Metab ; 63(5): 1204-10, 1986 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-3760120

RESUMO

To determine the source(s) of the excessive androgen production in patients with the polycystic ovary syndrome (PCOS), 12 hirsute women with PCOS underwent selective left adrenal and left ovarian venous catheterization. Blood samples were collected simultaneously for determination of cortisol, 17-hydroxy-progesterone, androstenedione (delta), testosterone (T), dehydroepiandrosterone, and dehydroepiandrosterone sulfate. The relative contributions of adrenal secretion rates of T and delta in each patient were estimated by relating their adrenal gradients to those of cortisol. From such calculations we found that in all patients the major source of androgens was the ovary (direct ovarian secretion and/or ovarian secretion of prehormones which then were converted to androgen in the peripheral circulation). After catheterization, 11 of the 12 patients underwent a 5-day dexamethasone suppression test (2 mg/day). In 7 patients studied, plasma delta and/or T levels decreased significantly. Our results indicate that in hirsutism associated with the PCOS, the predominant source of androgens is the ovaries and that glucocorticoid suppression cannot assign adrenal origin as the site of excessive androgens.


Assuntos
Glândulas Suprarrenais/irrigação sanguínea , Androgênios/biossíntese , Hirsutismo/sangue , Ovário/irrigação sanguínea , Síndrome do Ovário Policístico/sangue , Adolescente , Adulto , Androgênios/sangue , Androstenodiona/biossíntese , Cateterismo , Dexametasona , Feminino , Hirsutismo/etiologia , Humanos , Síndrome do Ovário Policístico/complicações , Testosterona/biossíntese
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