Epidemiology:
*Incidence:0.22/100000
*Frequent in neonates
*Risk factor:
# Pregnancy and puerperium
# Oral contraceptive pill
# ENT infection
# Cancer
# Prothrombitic states
# Dural AV fistula
Clinical features:
*Increased ICP as IIH
# Headche
# Visual obscurations
# Papilloedema
# CN VI palsy
*Focal neurological defecit:
# Hemiparesis
# Dysphasia
# Seizures
*Diffuse Encephalopathy:
# Delirium
# Coma
# Seizures
# Multifocal neurological defecit
*Cavernous Sinus Syndrome:
# CN III,IV,VI,V
# Proptosis
Investigations:
*Imaging: CT+ CT venogram or MRI+MR venogram
* Lumber puncture:
# After exclusion of mass lesion
# OP > 20 cm CSF
# Not necessary if diagnosis is definite after imaging
Management:
* Treat associated infection
*Anticoagulation with heparin followed by warfarin for 6 months.Lifelong if Prothrombitic conditions exist.
* If not responding or deteriorating,consider local thrombolysis therapy.
* Treatment of raised ICP:
# Repeated Lumber puncture or external lumber drain or lumboperitoneal shunt
# Mannitol
# If not Responding or deteriorating consider sedation, ventilation,and decompression craniectomy.
* Seizures:IV phenytoin or valproate
Reference:
1.Manji H, Connolly S, Kitchen N, Lambert C,Metha. Oxford handbook of Neurology: Neurological disorders.2nd edition. Oxford. Oxford University Press.2014
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