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1.
Braz. j. infect. dis ; 11(2): 297-299, Apr. 2007.
Artículo en Inglés | LILACS | ID: lil-454733

RESUMEN

Enterococci are an uncommon cause of CNS infection. A 20 month-old boy, diagnosed with hydrocephalus with ventriculoperitoneal shunt and history of lengthy hospitalization and use of wide spectrum antibiotics, was admitted to the pediatric intensive care unit diagnosed with ventriculitis. On the 14th day of empirical antibiotic therapy (vancomycin and meropenem) the child presented fever while the CSF sample culture evidenced vancomycin-resistant Enterococcus faecium. The patient received intravenous linezolid achieving cerebrospinal fluid sterilization. Conclusion: Intravenous linezolid appears to be a safe and effective therapy for vancomycin-resistant enterococcus ventriculoperitoneal shunt infection.


Asunto(s)
Humanos , Lactante , Masculino , Acetamidas/uso terapéutico , Antiinfecciosos/uso terapéutico , Ventrículos Cerebrales/microbiología , Encefalitis/tratamiento farmacológico , Enterococcus faecium/aislamiento & purificación , Infecciones por Bacterias Grampositivas/tratamiento farmacológico , Oxazolidinonas/uso terapéutico , Resistencia a la Vancomicina , Encefalitis/microbiología , Enterococcus faecium/efectos de los fármacos , Infecciones por Bacterias Grampositivas/microbiología , Hidrocefalia/tratamiento farmacológico , Hidrocefalia/microbiología , Resultado del Tratamiento , Derivación Ventriculoperitoneal
2.
Rev. Hosp. Clin. Fac. Med. Univ. Säo Paulo ; 55(1): 29-34, Jan.-Feb. 2000. ilus
Artículo en Inglés | LILACS | ID: lil-260705

RESUMEN

The blue rubber nevus syndrome consists of multiple venous malformations in the skin and gastrointestinal tract associated with intestinal hemorrhage and iron deficiency anemia. Other organs may be involved. The causes of this syndrome are unknown. Its most common presentation is in the form of sporadic cases, but dominant autosomal inheritance has been described. It is a condition that affects both sexes equally, and its occurrence is rare in the black race. We present a case of this syndrome diagnosed in a 11-year-old patient. He had severe anemia and a venous swelling on the trunk. Similar lesions were found in the stomach, bowel, and on his foot. We emphasize the main clinical aspects: intestine, eyes, nasopharynx, parotids, lungs, liver, spleen, heart, brain, pleura, peritoneum, pericardium, skeletal muscles, bladder, and penis lesions, systemic complications that may occur to these patients which are thrombosis and calcification, as well as consumptive coagulopathy and thrombocytopenia that may occur within the nevi.


Asunto(s)
Humanos , Masculino , Niño , Nevo Azul , Neoplasias Cutáneas , Anemia Ferropénica/diagnóstico , Sistema Digestivo/patología , Hemorragia Gastrointestinal/diagnóstico , Nevo Azul/complicaciones , Nevo Azul/diagnóstico , Síndrome
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