Hemolytic uremic syndrome (HUS),
characterized by the triad of micro-angiopathic hemolytic anemia,
thrombocytopenia, and acute renal insufficiency, is a common cause of acute
renal failure in children. It usually follows an episode of gastroenteritis with enterotoxigenic Escherichia coli and is termed typical HUS. However, HUS
is also a complication of invasive pneumococcal infection. Reasons for not
diagnosing this condition include the absence of a specific laboratory test,
the lack of consistent case definitions, unfamiliarity, a misdiagnosis of disseminated
intravascular coagulation (DIC), and cases with micro-angiopathic hemolytic
anemia and only mild renal injury.
The
aim of our study is to describe the epidemiology, the treatment and the
evolution of HUS after invasive pneumococcal infections in Tunisia. Cases were identified between 2008 and 2016. Infection with S. Pneumoniae was confirmed
with culture of cerebrospinal fluid, pleural fluid, or blood. Eight children
fulfilled our criteria for inclusion in the study. Primary patterns were fever,
respiratory signs, neurological signs and uncommon patterns. Pneumonia was a
presenting feature in 6 of 8 cases (75%), two patients had confirmed
pneumococcal meningitis.
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