RESUMO
Early diagnosis and prompt initiation of appropriate antimicrobial therapy are crucial steps in the management of patients with invasive fungal infections. However, the diagnosis of invasive mycoses remains a major challenge in clinical practice, because presenting symptoms may be subtle and non-invasive diagnostic assays often lack sensitivity and specificity. Diagnosis is often expressed on a scale of probability (proven, probable and possible) based on a constellation of imaging findings, microbiological tools and histopathology, as there is no stand-alone assay for diagnosis. Recent data suggest that the carbohydrate biomarker (1â3)-ß-d-glucan may be useful in both the diagnosis and therapeutic monitoring of invasive fungal infections due to some yeasts, molds, and dimorphic fungi. In this paper, we review recent advances in the use of (1â3)-ß-d-glucan to monitor clinical response to antifungal therapy and explore how this assay may be used in the future.
Assuntos
Antifúngicos/uso terapêutico , Infecções Fúngicas Invasivas/diagnóstico , Infecções Fúngicas Invasivas/tratamento farmacológico , beta-Glucanas/análise , Animais , Aspergilose/sangue , Aspergilose/líquido cefalorraquidiano , Aspergilose/diagnóstico , Aspergilose/tratamento farmacológico , Líquido da Lavagem Broncoalveolar/química , Candidíase/sangue , Candidíase/líquido cefalorraquidiano , Candidíase/diagnóstico , Candidíase/tratamento farmacológico , Humanos , Infecções Fúngicas Invasivas/sangue , Infecções Fúngicas Invasivas/líquido cefalorraquidiano , Meningite Fúngica/sangue , Meningite Fúngica/líquido cefalorraquidiano , Meningite Fúngica/diagnóstico , Meningite Fúngica/tratamento farmacológico , Pneumonia por Pneumocystis/sangue , Pneumonia por Pneumocystis/líquido cefalorraquidiano , Pneumonia por Pneumocystis/diagnóstico , Pneumonia por Pneumocystis/tratamento farmacológico , beta-Glucanas/sangue , beta-Glucanas/líquido cefalorraquidianoRESUMO
Progressive multifocal leukoencephalopathy (PML) is a demyelinating disease of the central nervous system caused by the JC polyomavirus. We describe a rare case of PML in a 48-year-old female patient with diffuse large B-cell lymphoma who received rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP) therapy. While she was undergoing five cycles of R-CHOP, she noticed gradually progressive neurological symptoms, such as slurred speech and gait disturbance, and she eventually developed high-grade fever. She also developed Pneumocystis jiroveci pneumonia. The neurological symptoms deteriorated thereafter, and she developed spastic quadriparesis and bulbar palsy. Magnetic resonance imaging showed hyperintensity within the right cerebellar hemisphere on T2-weighted images. Polymerase chain reaction-based tests of the cerebrospinal fluid revealed the presence of the JC virus. Despite intravenous and intrathecal cytarabine treatment, the patient died of PML 5 months after it was diagnosed. Retrospective analysis of her laboratory data showed that her CD4(+) T-cell count before R-CHOP therapy had decreased to 68 microL(-1). Thus, when administering rituximab-containing chemotherapy, even to patients with no prior history of opportunistic infections, attention should be paid to the potential occurrence of PML, particularly in patients with low CD4(+) T-cell counts.