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Revue Neurologique 2011-Mar

[Cerebral actinomycosis pseudotumor: a case report].

Aðeins skráðir notendur geta þýtt greinar
Skráðu þig / skráðu þig
Krækjan er vistuð á klemmuspjaldið
R Battikh
F M'Sadek
F Bougrine
W Madhi
N Ben Abdelhafidh
A Bouziani
M Yedeas
S Othmani

Lykilorð

Útdráttur

BACKGROUND

Cerebral actinomycosis is rare and difficult to diagnose.

METHODS

We report a case of a 45-year-old man hospitalized for seizures associated with fever and left hemiparesis. The white cell count and C-reactive protein were elevated. HIV serology was negative. Blood cultures remained sterile. The CT scan revealed hyperdense nodular lesions in the occipital area, with annular contrast uptake and peripheral edema causing a mass effect, suggestive of brain metastasis. The pathology examination of a surgical specimen disclosed cerebral actinomycosis. A dental origin of the infection was suspected. Hemiparesis remained after a 12-month antibiotic regimen associated with dental care and short-term corticosteroid therapy.

CONCLUSIONS

Actinomycosis should be discussed as a possible diagnosis for all cerebral lesions, particularly in patients with a potential dental infection. Histology is required for positive diagnosis. Antibiotic therapy alone is generally sufficient; surgery is often performed for diagnostic purposes.

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