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Osteoarticular infection by Candida albicans in an infant with cystic fibrosis
2011
Journal of Medical Microbiology
Invasive candidiasis is rare in children after the neonatal period, but can occur in children with (secondary) immunodeficiency with a damaged gastrointestinal or skin barrier, or when receiving antibiotics. A 10-month-old girl was diagnosed as suffering from cystic fibrosis (CF) when showing failure to thrive, pulmonary symptoms and hypoproteinaemia. At that time, Candida albicans was identified from blood culture and treated intravenously with liposomal amphotericin B for 13 days. Six weeks
doi:10.1099/jmm.0.031757-0
pmid:21596911
fatcat:f4bi6ukw5fc2bjdm5afzxfvl7m