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1.
Transpl Infect Dis ; 9(1): 66-72, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17313478

RESUMO

We report the case of a kidney transplant recipient who developed Lyme disease, followed by human granulocytic anaplasmosis (HGA) 3 years later. A review of all previously published cases of Lyme disease (3 cases), HGA (5 cases), and human monocytic ehrlichiosis (HME) (5 cases) in transplant recipients is presented. Manifestations of the cases reviewed were similar to those of non-transplant patients. There appeared to be no obvious correlation between immunosuppression and the occurrence of the illness in the transplant recipients. Serologic testing failed to make a diagnosis in 1 patient with HME in the literature and in our patient with HGA, but molecular tests established the diagnosis in both cases. Tandem infection was observed in 1 patient with two episodes of HME 2 years apart. A high index of suspicion for tick-borne illnesses and appropriate prevention measures are needed for transplant patients with epidemiologic risk factors.


Assuntos
Anaplasma phagocytophilum , Anaplasmose/etiologia , Borrelia burgdorferi , Imunossupressores/efeitos adversos , Transplante de Rim , Doença de Lyme/etiologia , Idoso , Rejeição de Enxerto/prevenção & controle , Humanos , Imunossupressores/administração & dosagem , Masculino , Literatura de Revisão como Assunto , Fatores de Risco
2.
Clin Microbiol Rev ; 19(1): 165-256, 2006 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-16418529

RESUMO

Real-time PCR has revolutionized the way clinical microbiology laboratories diagnose many human microbial infections. This testing method combines PCR chemistry with fluorescent probe detection of amplified product in the same reaction vessel. In general, both PCR and amplified product detection are completed in an hour or less, which is considerably faster than conventional PCR detection methods. Real-time PCR assays provide sensitivity and specificity equivalent to that of conventional PCR combined with Southern blot analysis, and since amplification and detection steps are performed in the same closed vessel, the risk of releasing amplified nucleic acids into the environment is negligible. The combination of excellent sensitivity and specificity, low contamination risk, and speed has made real-time PCR technology an appealing alternative to culture- or immunoassay-based testing methods for diagnosing many infectious diseases. This review focuses on the application of real-time PCR in the clinical microbiology laboratory.


Assuntos
Técnicas de Laboratório Clínico , Infecções/diagnóstico , Sondas de Oligonucleotídeos , Reação em Cadeia da Polimerase/métodos , Infecções Bacterianas/diagnóstico , Infecções Bacterianas/microbiologia , Humanos , Infecções/etiologia , Micoses/diagnóstico , Micoses/microbiologia , Infecções por Protozoários/diagnóstico , Infecções por Protozoários/parasitologia , Viroses/diagnóstico , Viroses/virologia
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