Data di Pubblicazione:
2022
Abstract:
OBJECTIVE: Human brucellosis
is a zoonosis with an extremely wide spectrum
of clinical manifestations. Focal splenic involvement
is very uncommon, particularly in the pediatric
age group, during the illness’ acute phase.
CASE REPORT: A 4-year-old boy, already receiving
third-generation cephalosporin treatment,
was transferred from a local hospital to
the University Pediatric Department for fever,
anemia, increased inflammation index, and multiple,
hyper-echogenic splenic lesions on abdominal
ultrasound. Initial diagnostic laboratory
investigations for Brucella infection, including
the Widal-Wright test, were found to be negative.
However, further diagnostic laboratory analysis
using the chemiluminescent immunoassay was
positive for Brucella IgM antibodies. Treatment
with rifampicin at a dose of 150 mg/Kg/twice
daily and co-trimethoprim at a dose of 80 mg/
Kg/twice daily was started and continued for 7
weeks. IgM antibodies were undetectable after
2 weeks of treatment, and after 6 weeks of treatment,
abdominal ultrasound documented a reduction
of the diameter of the major splenic infiltrate
from 1 to 0.5 cm. At 3 and 5 months of follow-
up, re-evaluation of the abdominal lesions
displayed complete resolution of the splenic lesions
and a complete clinical recovery.
CONCLUSIONS: The present case and a literature
review are presented in this study since
a standard diagnostic laboratory evaluation for
brucellosis may miss the diagnosis, and in suspected
cases, the laboratory analysis should be
extended. Splenic abscesses are known to be
rare in brucellosis, but the diagnosis should be
considered in children with severe focal lesions,
as specific antibiotic treatment may result in
complete clinical recovery.
Tipologia CRIS:
14.a.1 Articolo su rivista
Keywords:
Splenic abscess, Acute brucellosis, Childhood brucellosis,
Brucellosis treatment.
Elenco autori:
Pavone, P.; Gulizia, C.; D’Amico, S.; Grassi, P.; LA ROSA, G.; Leotta, R.; Basile, A.; Palmucci, S.; Foti, P. V.; Belfiore, G.; Marino, L.; Pellicanò, G. F.; Pulvirenti, G.
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