RESUMO
We present a case report of young man with Type 1 diabetes who developed acute visual loss after initially presenting with diabetic ketoacidosis. The diagnosis of invasive paranasal sinusoidal aspergillosis was made following CT and biopsy. Although uncommon, visual loss is a recognised complication of disseminated aspergillosis and is more likely in immune-compromised patients and those with diabetes. Early investigation with appropriate sinus imaging and involvement of the Ear Nose and Throat team in recommended when patients with diabetes develop acute visual loss in the context of a non-specific infective illness.
Assuntos
Aspergilose/complicações , Aspergilose/diagnóstico , Cegueira/complicações , Cegueira/microbiologia , Diabetes Mellitus Tipo 1/complicações , Serviço Hospitalar de Emergência , Doença Aguda , Anfotericina B/uso terapêutico , Antibacterianos/uso terapêutico , Antifúngicos/uso terapêutico , Aspergilose/tratamento farmacológico , Biópsia , Cegueira/diagnóstico , Caspofungina , Diagnóstico Diferencial , Equinocandinas/uso terapêutico , Evolução Fatal , Humanos , Lipopeptídeos , Imageamento por Ressonância Magnética/métodos , Masculino , Meropeném , Pessoa de Meia-Idade , Seios Paranasais/diagnóstico por imagem , Seios Paranasais/microbiologia , Seios Paranasais/patologia , Tienamicinas/uso terapêutico , Tomografia Computadorizada por Raios X/métodos , Reino UnidoRESUMO
We evaluated the in vitro activity of ramoplanin, an antimicrobial compound that inhibits cell wall synthesis by acting at the level of lipid intermediate formation, against Clostridium difficile. We included strains with reduced susceptibilities to vancomycin (vancomycin-intermediate [Van(i)] strains) or with resistance to metronidazole (Mtz(r)), in order to assess the potential utility of ramoplanin for the treatment of C. difficile-associated diarrhea. We tested the activity of ramoplanin against a total of 105 nonduplicate clinical isolates of toxigenic C. difficile, including 8 Van(i) isolates and 6 Mtz(r) isolates, obtained from our laboratory. Ramoplanin was active against all strains tested at concentrations ranging from 0.03 to 0.5 microg/ml (MICs at which 50 and 90% of isolates were inhibited, 0.25 microg/ml; geometric mean MIC, 0.22 microg/ml). All isolates, independently of their levels of susceptibility to vancomycin or metronidazole, were considered susceptible to ramoplanin (MICs, < or =0.5 microg/ml).