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Pan Afr Med J ; 28: 206, 2017.
Article in French | MEDLINE | ID: mdl-29610644

ABSTRACT

CVT is generally rare, particularly among infants. The occurrence of a SAH associated with CVT is very uncommon and only a few cases have been reported in the literature. Symptoms are variable and often misleading. Outcome can be lethal or it can cause potentially severe sequelae if it is not treated or treated late. We report the case of a 22-month old infant examined for convulsions with Stage II coma, intracranial hypertension syndrome and infectious syndrome. Laboratory tests showed pseudomonas spp sepsis and cerebral CT scan allowed the diagnosis. Treatment was based on antibiotic therapy but mainly on anticoagulation therapy. The patient had a significant clinical improvement and follow-up cerebral CT scan showed disappearance of thrombosis with sequellar right hemoragic images. CVT is a severe disease, usually of infectious origin. Anticoagulant therapy is controversial, in particular in patients with associated hemorrhage, but clinical experience supports the effectiveness and safety of this treatment.


Subject(s)
Intracranial Thrombosis/diagnosis , Pseudomonas Infections/diagnosis , Sepsis/diagnosis , Subarachnoid Hemorrhage/diagnosis , Anti-Bacterial Agents/therapeutic use , Anticoagulants/therapeutic use , Follow-Up Studies , Humans , Infant , Intracranial Thrombosis/drug therapy , Male , Pseudomonas Infections/drug therapy , Sepsis/drug therapy , Sepsis/microbiology , Subarachnoid Hemorrhage/drug therapy , Tomography, X-Ray Computed
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