Abstract

We report the first case of primary amebic meningoencephalitis in Italy, in a 9-year-old boy. Clinical course was fulminant, and diagnosis was made by identifying amebas in stained brain sections and by indirect immunofluorescence analysis. Naegleria fowleri was characterized as genotype I on the basis of polymerase chain reaction test results.

Highlights

  • Primary amebic meningoencephalitis (PAM) is invariably an acute, often fulminant infection caused by Naegleria fowleri, a small, free-living ameba that occasionally infects humans and other mammals

  • DNA was extracted with 500 μL of Conclusions As the clinical and epidemiologic history demonstrate, our patient contracted PAM caused by N. fowleri 10 days after swimming and diving in polluted river water in Italy during the unusually hot summer

  • Though not strictly specific, clinical features of PAM (1,2): 1) hyperacute clinical course; 2) unrelenting signs and symptoms of meningitis and encephalitis, the latter confirmed by computed tomographic (CT) imaging; 3) high levels of peripheral leukocyte count, mainly polymorphonuclear leukocytes; 4) cloudy cerebrospinal fluid (CSF) with leukocytes, hyperproteinosis, low glucose level, and absence of bacteria and fungi; 5) rapid worsening of disease, leading to death within a week

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Summary

Introduction

Primary amebic meningoencephalitis (PAM) is invariably an acute, often fulminant infection caused by Naegleria fowleri, a small, free-living ameba that occasionally infects humans and other mammals. Sion, the patient was febrile (temperature 38°C), with a total leukocyte count of 13,780/mm[3] and C-reactive protein level of 1.2 mg/L. A lumbar puncture showed cloudy cerebrospinal fluid (CSF) with 2.5 mmol/L glucose, 4.54 g/L protein, and a leukocyte count of 6,800/mm[3] with 90% neutrophils.

Results
Conclusion

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