Intracranial haematomas I . Extra dural haematomas :- between the dura & the skull middle meningeal artery Common site is temporal fossa . TRAUMA
INVESTIGATIONS: CT ( Biconvex hyperdense lesion ) MRI CEREBRAL ANGIOGRAPHY Treatment: Surgical evacuation followed by Craniotomy
II. Subdural haematomas :- between the dura and the arachnoid . Common causes are bleeding from superficial veins or venous sinuses. Anticoagulant treatment predispose to intracranial bleeding and subdural haematoma .
Clinical features: Acute : Clinical features are similar to extra dural hematoma. Chronic : Dementia, altered behaviour , psychiatric manifestations or focal neurological deficits may develop. In middle aged headache, contralateral hemiplegia , papilledema children: vomiting, restlessness. Irritability, refusal to feed, anaemia , seizures and failure to thrive.
Treatment: Craniotomy for Acute Subdural Hematoma Surgical evacuation by Burr hole for chronic subdural hematoma . DIAGNOSIS: Acute-concave hyperdense lesion on CT Chronic- 0-10days( hyperdense ) 10days-2wks( isodense ) >2wks( hypodense ) lesions on CT .
BRAIN ABSCESS Mostly single may be multiple Majority Supratentorial , 10% infratentorial Metastatic: hematogenesis,direct spread from adjacent structures or penetrating brain injury.
DIAGNOSIS Method of Choice- CT scan of Brain Ring enhancing Lesion Peripheral Blood smear Leukocytosis Raised ESR
TREATMENT SPECIFIC TREATMENT Anti-microbial therapy MEASURES TO REDUCE ICP Drainage of abscess Mannitol corticosteroids ANTI-EPILEPTIC TREATMENT Phenytoin Carbamazapine
SURGICAL TREATMENT GOALS: Obtain pus for culture & sensitivity Decrease ICP TECHNIQUES: Burr hole & aspiration Excision & craniotomy for recurrent, thickwalled brain abscess.
INTRACRANIAL TUBERCULOMA Mostly in developing countries caused by Micro-bacterium tuberculus . Nodular or irregular avascular masses of variable sizes surrounded by edema. Frequently multiple Common location: sub-cortical in cerebral hemisphere.
Clinical presentation Symptoms & signs of progressive intracranial SOL : Raised ICP Focal neurologic deficits Seizures etc General malaise,fever in 50% patients.
INVESTIGATIONS Lab work-up Leukocytosis ESR- raised or normal Mantox test- often+ve Chest X-ray Plain skull X-ray CT & MRI- Investigation of choice Hyper-dense masses with ring and surroundind edema, often”Target sign”
TREATMENT Anti-tubercular therapy Measures to reduce ICP Control seizure
INDICATIONS: Intracranial lesions could not be specified Progressive neurological detoriation ALTERNATIVES: Excision: CSF-shunting: mandatory in complicating obstructive hydrocephalus SURGICAL TREATMENT