L. Klingspor et al., DEEP CANDIDA INFECTION IN CHILDREN WITH LEUKEMIA - CLINICAL PRESENTATIONS, DIAGNOSIS AND OUTCOME, Acta paediatrica, 86(1), 1997, pp. 30-36
Objectives: To analyse the clinical features associated with deep Cand
ida infection (DCI) and the outcome in children with leukaemia, and to
evaluate. various diagnostic methods. Materials and methods: Serum sa
mples were analysed to determine Candida IgA, IgM and IgG antibodies a
nd detect free C, albicans glucoprotein antigen and C. enolase antigen
in eight children who had nine episodes of DCI and six with suspected
DCI. Results: DCI occurred shortly after the leukaemia diagnosis (med
ian 40 days) or after the leukaemia relapse (median 30 days). Children
with DCI had fever (100%), skin lesions/exanthema (45%), oral thrush
(45%), oesophagitis (22%) and laryngo-tracheitis (22%). Candida endoca
rditis, arthritis and hepatic candidosis were diagnosed in one patient
each. Two children with disseminated candidosis died in leukaemia rel
apse. in patients with C. albicans infections serology had a sensitivi
ty of 83%. However, in patients with C. parapsilosis infection antibod
y detection was negative. As the patients were cured of their Candida
infection, the IgG antibodies disappeared and the IgM and IgA antibodi
es fell within the normal range for age. Conclusion: DCI in children o
ccurs shortly after the leukaemia diagnosis or shortly after relapse o
f leukaemia. The clinical features are many. Candida serology may help
to diagnose or confirm DCI. The dynamics of antibody titres may help
to establish the efficacy of antifungal treatment.