Abstract
AbstractCystic echinococcosis is a major public health concern, particularly in endemic areas. The primary cerebral hydatid cyst is rare. Specific diagnosis is mainly based on microscopic examinations of the cyst fluid. Prognosis is usually benign after surgery. Nevertheless, surgical rupture may cause complications including anaphylactic shock, recurrence or dissemination. We report a solitary and primary cerebral hydatid cyst, revealed by intracranial hypertension and gait disorders in a 7-year-old boy. Despite per-operative rupture of the cyst, the child has evolved well with a follow-up of six months.
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